hypothesis testing in statistics definition

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In today’s data-driven world , decisions are based on data all the time. Hypothesis plays a crucial role in that process, whether it may be making business decisions, in the health sector, academia, or in quality improvement. Without hypothesis & hypothesis tests, you risk drawing the wrong conclusions and making bad decisions. In this tutorial, you will look at Hypothesis Testing in Statistics.

What Is Hypothesis Testing in Statistics?

Hypothesis Testing is a type of statistical analysis in which you put your assumptions about a population parameter to the test. It is used to estimate the relationship between 2 statistical variables.

Let's discuss few examples of statistical hypothesis from real-life - 

• A teacher assumes that 60% of his college's students come from lower-middle-class families.
• A doctor believes that 3D (Diet, Dose, and Discipline) is 90% effective for diabetic patients.

Now that you know about hypothesis testing, look at the two types of hypothesis testing in statistics.

Hypothesis Testing Formula

Z = ( x̅ – μ0 ) / (σ /√n)

• Here, x̅ is the sample mean,
• μ0 is the population mean,
• σ is the standard deviation,
• n is the sample size.

How Hypothesis Testing Works?

An analyst performs hypothesis testing on a statistical sample to present evidence of the plausibility of the null hypothesis. Measurements and analyses are conducted on a random sample of the population to test a theory. Analysts use a random population sample to test two hypotheses: the null and alternative hypotheses.

The null hypothesis is typically an equality hypothesis between population parameters; for example, a null hypothesis may claim that the population means return equals zero. The alternate hypothesis is essentially the inverse of the null hypothesis (e.g., the population means the return is not equal to zero). As a result, they are mutually exclusive, and only one can be correct. One of the two possibilities, however, will always be correct.

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Null Hypothesis and Alternate Hypothesis

The Null Hypothesis is the assumption that the event will not occur. A null hypothesis has no bearing on the study's outcome unless it is rejected.

H0 is the symbol for it, and it is pronounced H-naught.

The Alternate Hypothesis is the logical opposite of the null hypothesis. The acceptance of the alternative hypothesis follows the rejection of the null hypothesis. H1 is the symbol for it.

Let's understand this with an example.

A sanitizer manufacturer claims that its product kills 95 percent of germs on average. 

To put this company's claim to the test, create a null and alternate hypothesis.

H0 (Null Hypothesis): Average = 95%.

Alternative Hypothesis (H1): The average is less than 95%.

Another straightforward example to understand this concept is determining whether or not a coin is fair and balanced. The null hypothesis states that the probability of a show of heads is equal to the likelihood of a show of tails. In contrast, the alternate theory states that the probability of a show of heads and tails would be very different.

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Hypothesis Testing Calculation With Examples

Let's consider a hypothesis test for the average height of women in the United States. Suppose our null hypothesis is that the average height is 5'4". We gather a sample of 100 women and determine that their average height is 5'5". The standard deviation of population is 2.

To calculate the z-score, we would use the following formula:

z = ( x̅ – μ0 ) / (σ /√n)

z = (5'5" - 5'4") / (2" / √100)

z = 0.5 / (0.045)

 We will reject the null hypothesis as the z-score of 11.11 is very large and conclude that there is evidence to suggest that the average height of women in the US is greater than 5'4".

Steps of Hypothesis Testing

Step 1: specify your null and alternate hypotheses.

It is critical to rephrase your original research hypothesis (the prediction that you wish to study) as a null (Ho) and alternative (Ha) hypothesis so that you can test it quantitatively. Your first hypothesis, which predicts a link between variables, is generally your alternate hypothesis. The null hypothesis predicts no link between the variables of interest.

Step 2: Gather Data

For a statistical test to be legitimate, sampling and data collection must be done in a way that is meant to test your hypothesis. You cannot draw statistical conclusions about the population you are interested in if your data is not representative.

Step 3: Conduct a Statistical Test

Other statistical tests are available, but they all compare within-group variance (how to spread out the data inside a category) against between-group variance (how different the categories are from one another). If the between-group variation is big enough that there is little or no overlap between groups, your statistical test will display a low p-value to represent this. This suggests that the disparities between these groups are unlikely to have occurred by accident. Alternatively, if there is a large within-group variance and a low between-group variance, your statistical test will show a high p-value. Any difference you find across groups is most likely attributable to chance. The variety of variables and the level of measurement of your obtained data will influence your statistical test selection.

Step 4: Determine Rejection Of Your Null Hypothesis

Your statistical test results must determine whether your null hypothesis should be rejected or not. In most circumstances, you will base your judgment on the p-value provided by the statistical test. In most circumstances, your preset level of significance for rejecting the null hypothesis will be 0.05 - that is, when there is less than a 5% likelihood that these data would be seen if the null hypothesis were true. In other circumstances, researchers use a lower level of significance, such as 0.01 (1%). This reduces the possibility of wrongly rejecting the null hypothesis.

Step 5: Present Your Results 

The findings of hypothesis testing will be discussed in the results and discussion portions of your research paper, dissertation, or thesis. You should include a concise overview of the data and a summary of the findings of your statistical test in the results section. You can talk about whether your results confirmed your initial hypothesis or not in the conversation. Rejecting or failing to reject the null hypothesis is a formal term used in hypothesis testing. This is likely a must for your statistics assignments.

Types of Hypothesis Testing

To determine whether a discovery or relationship is statistically significant, hypothesis testing uses a z-test. It usually checks to see if two means are the same (the null hypothesis). Only when the population standard deviation is known and the sample size is 30 data points or more, can a z-test be applied.

A statistical test called a t-test is employed to compare the means of two groups. To determine whether two groups differ or if a procedure or treatment affects the population of interest, it is frequently used in hypothesis testing.

Chi-Square 

You utilize a Chi-square test for hypothesis testing concerning whether your data is as predicted. To determine if the expected and observed results are well-fitted, the Chi-square test analyzes the differences between categorical variables from a random sample. The test's fundamental premise is that the observed values in your data should be compared to the predicted values that would be present if the null hypothesis were true.

Hypothesis Testing and Confidence Intervals

Both confidence intervals and hypothesis tests are inferential techniques that depend on approximating the sample distribution. Data from a sample is used to estimate a population parameter using confidence intervals. Data from a sample is used in hypothesis testing to examine a given hypothesis. We must have a postulated parameter to conduct hypothesis testing.

Bootstrap distributions and randomization distributions are created using comparable simulation techniques. The observed sample statistic is the focal point of a bootstrap distribution, whereas the null hypothesis value is the focal point of a randomization distribution.

A variety of feasible population parameter estimates are included in confidence ranges. In this lesson, we created just two-tailed confidence intervals. There is a direct connection between these two-tail confidence intervals and these two-tail hypothesis tests. The results of a two-tailed hypothesis test and two-tailed confidence intervals typically provide the same results. In other words, a hypothesis test at the 0.05 level will virtually always fail to reject the null hypothesis if the 95% confidence interval contains the predicted value. A hypothesis test at the 0.05 level will nearly certainly reject the null hypothesis if the 95% confidence interval does not include the hypothesized parameter.

Simple and Composite Hypothesis Testing

Depending on the population distribution, you can classify the statistical hypothesis into two types.

Simple Hypothesis: A simple hypothesis specifies an exact value for the parameter.

Composite Hypothesis: A composite hypothesis specifies a range of values.

A company is claiming that their average sales for this quarter are 1000 units. This is an example of a simple hypothesis.

Suppose the company claims that the sales are in the range of 900 to 1000 units. Then this is a case of a composite hypothesis.

One-Tailed and Two-Tailed Hypothesis Testing

The One-Tailed test, also called a directional test, considers a critical region of data that would result in the null hypothesis being rejected if the test sample falls into it, inevitably meaning the acceptance of the alternate hypothesis.

In a one-tailed test, the critical distribution area is one-sided, meaning the test sample is either greater or lesser than a specific value.

In two tails, the test sample is checked to be greater or less than a range of values in a Two-Tailed test, implying that the critical distribution area is two-sided.

If the sample falls within this range, the alternate hypothesis will be accepted, and the null hypothesis will be rejected.

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Right Tailed Hypothesis Testing

If the larger than (>) sign appears in your hypothesis statement, you are using a right-tailed test, also known as an upper test. Or, to put it another way, the disparity is to the right. For instance, you can contrast the battery life before and after a change in production. Your hypothesis statements can be the following if you want to know if the battery life is longer than the original (let's say 90 hours):

• The null hypothesis is (H0 <= 90) or less change.
• A possibility is that battery life has risen (H1) > 90.

The crucial point in this situation is that the alternate hypothesis (H1), not the null hypothesis, decides whether you get a right-tailed test.

Left Tailed Hypothesis Testing

Alternative hypotheses that assert the true value of a parameter is lower than the null hypothesis are tested with a left-tailed test; they are indicated by the asterisk "<".

Suppose H0: mean = 50 and H1: mean not equal to 50

According to the H1, the mean can be greater than or less than 50. This is an example of a Two-tailed test.

In a similar manner, if H0: mean >=50, then H1: mean <50

Here the mean is less than 50. It is called a One-tailed test.

Type 1 and Type 2 Error

A hypothesis test can result in two types of errors.

Type 1 Error: A Type-I error occurs when sample results reject the null hypothesis despite being true.

Type 2 Error: A Type-II error occurs when the null hypothesis is not rejected when it is false, unlike a Type-I error.

Suppose a teacher evaluates the examination paper to decide whether a student passes or fails.

H0: Student has passed

H1: Student has failed

Type I error will be the teacher failing the student [rejects H0] although the student scored the passing marks [H0 was true]. 

Type II error will be the case where the teacher passes the student [do not reject H0] although the student did not score the passing marks [H1 is true].

Level of Significance

The alpha value is a criterion for determining whether a test statistic is statistically significant. In a statistical test, Alpha represents an acceptable probability of a Type I error. Because alpha is a probability, it can be anywhere between 0 and 1. In practice, the most commonly used alpha values are 0.01, 0.05, and 0.1, which represent a 1%, 5%, and 10% chance of a Type I error, respectively (i.e. rejecting the null hypothesis when it is in fact correct).

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A p-value is a metric that expresses the likelihood that an observed difference could have occurred by chance. As the p-value decreases the statistical significance of the observed difference increases. If the p-value is too low, you reject the null hypothesis.

Here you have taken an example in which you are trying to test whether the new advertising campaign has increased the product's sales. The p-value is the likelihood that the null hypothesis, which states that there is no change in the sales due to the new advertising campaign, is true. If the p-value is .30, then there is a 30% chance that there is no increase or decrease in the product's sales.  If the p-value is 0.03, then there is a 3% probability that there is no increase or decrease in the sales value due to the new advertising campaign. As you can see, the lower the p-value, the chances of the alternate hypothesis being true increases, which means that the new advertising campaign causes an increase or decrease in sales.

Why is Hypothesis Testing Important in Research Methodology?

Hypothesis testing is crucial in research methodology for several reasons:

• Provides evidence-based conclusions: It allows researchers to make objective conclusions based on empirical data, providing evidence to support or refute their research hypotheses.
• Supports decision-making: It helps make informed decisions, such as accepting or rejecting a new treatment, implementing policy changes, or adopting new practices.
• Adds rigor and validity: It adds scientific rigor to research using statistical methods to analyze data, ensuring that conclusions are based on sound statistical evidence.
• Contributes to the advancement of knowledge: By testing hypotheses, researchers contribute to the growth of knowledge in their respective fields by confirming existing theories or discovering new patterns and relationships.

Limitations of Hypothesis Testing

Hypothesis testing has some limitations that researchers should be aware of:

• It cannot prove or establish the truth: Hypothesis testing provides evidence to support or reject a hypothesis, but it cannot confirm the absolute truth of the research question.
• Results are sample-specific: Hypothesis testing is based on analyzing a sample from a population, and the conclusions drawn are specific to that particular sample.
• Possible errors: During hypothesis testing, there is a chance of committing type I error (rejecting a true null hypothesis) or type II error (failing to reject a false null hypothesis).
• Assumptions and requirements: Different tests have specific assumptions and requirements that must be met to accurately interpret results.

After reading this tutorial, you would have a much better understanding of hypothesis testing, one of the most important concepts in the field of Data Science . The majority of hypotheses are based on speculation about observed behavior, natural phenomena, or established theories.

If you are interested in statistics of data science and skills needed for such a career, you ought to explore Simplilearn’s Post Graduate Program in Data Science.

If you have any questions regarding this ‘Hypothesis Testing In Statistics’ tutorial, do share them in the comment section. Our subject matter expert will respond to your queries. Happy learning!

1. What is hypothesis testing in statistics with example?

Hypothesis testing is a statistical method used to determine if there is enough evidence in a sample data to draw conclusions about a population. It involves formulating two competing hypotheses, the null hypothesis (H0) and the alternative hypothesis (Ha), and then collecting data to assess the evidence. An example: testing if a new drug improves patient recovery (Ha) compared to the standard treatment (H0) based on collected patient data.

2. What is hypothesis testing and its types?

Hypothesis testing is a statistical method used to make inferences about a population based on sample data. It involves formulating two hypotheses: the null hypothesis (H0), which represents the default assumption, and the alternative hypothesis (Ha), which contradicts H0. The goal is to assess the evidence and determine whether there is enough statistical significance to reject the null hypothesis in favor of the alternative hypothesis.

Types of hypothesis testing:

• One-sample test: Used to compare a sample to a known value or a hypothesized value.
• Two-sample test: Compares two independent samples to assess if there is a significant difference between their means or distributions.
• Paired-sample test: Compares two related samples, such as pre-test and post-test data, to evaluate changes within the same subjects over time or under different conditions.
• Chi-square test: Used to analyze categorical data and determine if there is a significant association between variables.
• ANOVA (Analysis of Variance): Compares means across multiple groups to check if there is a significant difference between them.

3. What are the steps of hypothesis testing?

The steps of hypothesis testing are as follows:

• Formulate the hypotheses: State the null hypothesis (H0) and the alternative hypothesis (Ha) based on the research question.
• Set the significance level: Determine the acceptable level of error (alpha) for making a decision.
• Collect and analyze data: Gather and process the sample data.
• Compute test statistic: Calculate the appropriate statistical test to assess the evidence.
• Make a decision: Compare the test statistic with critical values or p-values and determine whether to reject H0 in favor of Ha or not.
• Draw conclusions: Interpret the results and communicate the findings in the context of the research question.

4. What are the 2 types of hypothesis testing?

• One-tailed (or one-sided) test: Tests for the significance of an effect in only one direction, either positive or negative.
• Two-tailed (or two-sided) test: Tests for the significance of an effect in both directions, allowing for the possibility of a positive or negative effect.

The choice between one-tailed and two-tailed tests depends on the specific research question and the directionality of the expected effect.

5. What are the 3 major types of hypothesis?

The three major types of hypotheses are:

• Null Hypothesis (H0): Represents the default assumption, stating that there is no significant effect or relationship in the data.
• Alternative Hypothesis (Ha): Contradicts the null hypothesis and proposes a specific effect or relationship that researchers want to investigate.
• Nondirectional Hypothesis: An alternative hypothesis that doesn't specify the direction of the effect, leaving it open for both positive and negative possibilities.

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Avijeet is a Senior Research Analyst at Simplilearn. Passionate about Data Analytics, Machine Learning, and Deep Learning, Avijeet is also interested in politics, cricket, and football.

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Statistics Made Easy

Introduction to Hypothesis Testing

A statistical hypothesis is an assumption about a population parameter .

For example, we may assume that the mean height of a male in the U.S. is 70 inches.

The assumption about the height is the statistical hypothesis and the true mean height of a male in the U.S. is the population parameter .

A hypothesis test is a formal statistical test we use to reject or fail to reject a statistical hypothesis.

The Two Types of Statistical Hypotheses

To test whether a statistical hypothesis about a population parameter is true, we obtain a random sample from the population and perform a hypothesis test on the sample data.

There are two types of statistical hypotheses:

The null hypothesis , denoted as H 0 , is the hypothesis that the sample data occurs purely from chance.

The alternative hypothesis , denoted as H 1 or H a , is the hypothesis that the sample data is influenced by some non-random cause.

Hypothesis Tests

A hypothesis test consists of five steps:

1. State the hypotheses. 

State the null and alternative hypotheses. These two hypotheses need to be mutually exclusive, so if one is true then the other must be false.

2. Determine a significance level to use for the hypothesis.

Decide on a significance level. Common choices are .01, .05, and .1. 

3. Find the test statistic.

Find the test statistic and the corresponding p-value. Often we are analyzing a population mean or proportion and the general formula to find the test statistic is: (sample statistic – population parameter) / (standard deviation of statistic)

4. Reject or fail to reject the null hypothesis.

Using the test statistic or the p-value, determine if you can reject or fail to reject the null hypothesis based on the significance level.

The p-value  tells us the strength of evidence in support of a null hypothesis. If the p-value is less than the significance level, we reject the null hypothesis.

5. Interpret the results. 

Interpret the results of the hypothesis test in the context of the question being asked. 

The Two Types of Decision Errors

There are two types of decision errors that one can make when doing a hypothesis test:

Type I error: You reject the null hypothesis when it is actually true. The probability of committing a Type I error is equal to the significance level, often called  alpha , and denoted as α.

Type II error: You fail to reject the null hypothesis when it is actually false. The probability of committing a Type II error is called the Power of the test or  Beta , denoted as β.

One-Tailed and Two-Tailed Tests

A statistical hypothesis can be one-tailed or two-tailed.

A one-tailed hypothesis involves making a “greater than” or “less than ” statement.

For example, suppose we assume the mean height of a male in the U.S. is greater than or equal to 70 inches. The null hypothesis would be H0: µ ≥ 70 inches and the alternative hypothesis would be Ha: µ < 70 inches.

A two-tailed hypothesis involves making an “equal to” or “not equal to” statement.

For example, suppose we assume the mean height of a male in the U.S. is equal to 70 inches. The null hypothesis would be H0: µ = 70 inches and the alternative hypothesis would be Ha: µ ≠ 70 inches.

Note: The “equal” sign is always included in the null hypothesis, whether it is =, ≥, or ≤.

Related:   What is a Directional Hypothesis?

Types of Hypothesis Tests

There are many different types of hypothesis tests you can perform depending on the type of data you’re working with and the goal of your analysis.

The following tutorials provide an explanation of the most common types of hypothesis tests:

Introduction to the One Sample t-test Introduction to the Two Sample t-test Introduction to the Paired Samples t-test Introduction to the One Proportion Z-Test Introduction to the Two Proportion Z-Test

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• Fundamental Analysis

Hypothesis to Be Tested: Definition and 4 Steps for Testing with Example

What Is Hypothesis Testing?

Hypothesis testing, sometimes called significance testing, is an act in statistics whereby an analyst tests an assumption regarding a population parameter. The methodology employed by the analyst depends on the nature of the data used and the reason for the analysis.

Hypothesis testing is used to assess the plausibility of a hypothesis by using sample data. Such data may come from a larger population, or from a data-generating process. The word "population" will be used for both of these cases in the following descriptions.

Key Takeaways

• Hypothesis testing is used to assess the plausibility of a hypothesis by using sample data.
• The test provides evidence concerning the plausibility of the hypothesis, given the data.
• Statistical analysts test a hypothesis by measuring and examining a random sample of the population being analyzed.
• The four steps of hypothesis testing include stating the hypotheses, formulating an analysis plan, analyzing the sample data, and analyzing the result.

How Hypothesis Testing Works

In hypothesis testing, an  analyst  tests a statistical sample, with the goal of providing evidence on the plausibility of the null hypothesis.

Statistical analysts test a hypothesis by measuring and examining a random sample of the population being analyzed. All analysts use a random population sample to test two different hypotheses: the null hypothesis and the alternative hypothesis.

The null hypothesis is usually a hypothesis of equality between population parameters; e.g., a null hypothesis may state that the population mean return is equal to zero. The alternative hypothesis is effectively the opposite of a null hypothesis (e.g., the population mean return is not equal to zero). Thus, they are mutually exclusive , and only one can be true. However, one of the two hypotheses will always be true.

The null hypothesis is a statement about a population parameter, such as the population mean, that is assumed to be true.

4 Steps of Hypothesis Testing

All hypotheses are tested using a four-step process:

• The first step is for the analyst to state the hypotheses.
• The second step is to formulate an analysis plan, which outlines how the data will be evaluated.
• The third step is to carry out the plan and analyze the sample data.
• The final step is to analyze the results and either reject the null hypothesis, or state that the null hypothesis is plausible, given the data.

Real-World Example of Hypothesis Testing

If, for example, a person wants to test that a penny has exactly a 50% chance of landing on heads, the null hypothesis would be that 50% is correct, and the alternative hypothesis would be that 50% is not correct.

Mathematically, the null hypothesis would be represented as Ho: P = 0.5. The alternative hypothesis would be denoted as "Ha" and be identical to the null hypothesis, except with the equal sign struck-through, meaning that it does not equal 50%.

A random sample of 100 coin flips is taken, and the null hypothesis is then tested. If it is found that the 100 coin flips were distributed as 40 heads and 60 tails, the analyst would assume that a penny does not have a 50% chance of landing on heads and would reject the null hypothesis and accept the alternative hypothesis.

If, on the other hand, there were 48 heads and 52 tails, then it is plausible that the coin could be fair and still produce such a result. In cases such as this where the null hypothesis is "accepted," the analyst states that the difference between the expected results (50 heads and 50 tails) and the observed results (48 heads and 52 tails) is "explainable by chance alone."

Some staticians attribute the first hypothesis tests to satirical writer John Arbuthnot in 1710, who studied male and female births in England after observing that in nearly every year, male births exceeded female births by a slight proportion. Arbuthnot calculated that the probability of this happening by chance was small, and therefore it was due to “divine providence.”

What is Hypothesis Testing?

Hypothesis testing refers to a process used by analysts to assess the plausibility of a hypothesis by using sample data. In hypothesis testing, statisticians formulate two hypotheses: the null hypothesis and the alternative hypothesis. A null hypothesis determines there is no difference between two groups or conditions, while the alternative hypothesis determines that there is a difference. Researchers evaluate the statistical significance of the test based on the probability that the null hypothesis is true.

What are the Four Key Steps Involved in Hypothesis Testing?

Hypothesis testing begins with an analyst stating two hypotheses, with only one that can be right. The analyst then formulates an analysis plan, which outlines how the data will be evaluated. Next, they move to the testing phase and analyze the sample data. Finally, the analyst analyzes the results and either rejects the null hypothesis or states that the null hypothesis is plausible, given the data.

What are the Benefits of Hypothesis Testing?

Hypothesis testing helps assess the accuracy of new ideas or theories by testing them against data. This allows researchers to determine whether the evidence supports their hypothesis, helping to avoid false claims and conclusions. Hypothesis testing also provides a framework for decision-making based on data rather than personal opinions or biases. By relying on statistical analysis, hypothesis testing helps to reduce the effects of chance and confounding variables, providing a robust framework for making informed conclusions.

What are the Limitations of Hypothesis Testing?

Hypothesis testing relies exclusively on data and doesn’t provide a comprehensive understanding of the subject being studied. Additionally, the accuracy of the results depends on the quality of the available data and the statistical methods used. Inaccurate data or inappropriate hypothesis formulation may lead to incorrect conclusions or failed tests. Hypothesis testing can also lead to errors, such as analysts either accepting or rejecting a null hypothesis when they shouldn’t have. These errors may result in false conclusions or missed opportunities to identify significant patterns or relationships in the data.

The Bottom Line

Hypothesis testing refers to a statistical process that helps researchers and/or analysts determine the reliability of a study. By using a well-formulated hypothesis and set of statistical tests, individuals or businesses can make inferences about the population that they are studying and draw conclusions based on the data presented. There are different types of hypothesis testing, each with their own set of rules and procedures. However, all hypothesis testing methods have the same four step process, which includes stating the hypotheses, formulating an analysis plan, analyzing the sample data, and analyzing the result. Hypothesis testing plays a vital part of the scientific process, helping to test assumptions and make better data-based decisions.

Sage. " Introduction to Hypothesis Testing. " Page 4.

Elder Research. " Who Invented the Null Hypothesis? "

Formplus. " Hypothesis Testing: Definition, Uses, Limitations and Examples. "

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Unit 12: Significance tests (hypothesis testing)

About this unit, the idea of significance tests.

• Simple hypothesis testing (Opens a modal)
• Idea behind hypothesis testing (Opens a modal)
• Examples of null and alternative hypotheses (Opens a modal)
• P-values and significance tests (Opens a modal)
• Comparing P-values to different significance levels (Opens a modal)
• Estimating a P-value from a simulation (Opens a modal)
• Using P-values to make conclusions (Opens a modal)
• Simple hypothesis testing Get 3 of 4 questions to level up!
• Writing null and alternative hypotheses Get 3 of 4 questions to level up!
• Estimating P-values from simulations Get 3 of 4 questions to level up!

Error probabilities and power

• Introduction to Type I and Type II errors (Opens a modal)
• Type 1 errors (Opens a modal)
• Examples identifying Type I and Type II errors (Opens a modal)
• Introduction to power in significance tests (Opens a modal)
• Examples thinking about power in significance tests (Opens a modal)
• Consequences of errors and significance (Opens a modal)
• Type I vs Type II error Get 3 of 4 questions to level up!
• Error probabilities and power Get 3 of 4 questions to level up!

Tests about a population proportion

• Constructing hypotheses for a significance test about a proportion (Opens a modal)
• Conditions for a z test about a proportion (Opens a modal)
• Reference: Conditions for inference on a proportion (Opens a modal)
• Calculating a z statistic in a test about a proportion (Opens a modal)
• Calculating a P-value given a z statistic (Opens a modal)
• Making conclusions in a test about a proportion (Opens a modal)
• Writing hypotheses for a test about a proportion Get 3 of 4 questions to level up!
• Conditions for a z test about a proportion Get 3 of 4 questions to level up!
• Calculating the test statistic in a z test for a proportion Get 3 of 4 questions to level up!
• Calculating the P-value in a z test for a proportion Get 3 of 4 questions to level up!
• Making conclusions in a z test for a proportion Get 3 of 4 questions to level up!

Tests about a population mean

• Writing hypotheses for a significance test about a mean (Opens a modal)
• Conditions for a t test about a mean (Opens a modal)
• Reference: Conditions for inference on a mean (Opens a modal)
• When to use z or t statistics in significance tests (Opens a modal)
• Example calculating t statistic for a test about a mean (Opens a modal)
• Using TI calculator for P-value from t statistic (Opens a modal)
• Using a table to estimate P-value from t statistic (Opens a modal)
• Comparing P-value from t statistic to significance level (Opens a modal)
• Free response example: Significance test for a mean (Opens a modal)
• Writing hypotheses for a test about a mean Get 3 of 4 questions to level up!
• Conditions for a t test about a mean Get 3 of 4 questions to level up!
• Calculating the test statistic in a t test for a mean Get 3 of 4 questions to level up!
• Calculating the P-value in a t test for a mean Get 3 of 4 questions to level up!
• Making conclusions in a t test for a mean Get 3 of 4 questions to level up!

More significance testing videos

• Hypothesis testing and p-values (Opens a modal)
• One-tailed and two-tailed tests (Opens a modal)
• Z-statistics vs. T-statistics (Opens a modal)
• Small sample hypothesis test (Opens a modal)
• Large sample proportion hypothesis testing (Opens a modal)

Hypothesis Testing

Hypothesis testing is a tool for making statistical inferences about the population data. It is an analysis tool that tests assumptions and determines how likely something is within a given standard of accuracy. Hypothesis testing provides a way to verify whether the results of an experiment are valid.

A null hypothesis and an alternative hypothesis are set up before performing the hypothesis testing. This helps to arrive at a conclusion regarding the sample obtained from the population. In this article, we will learn more about hypothesis testing, its types, steps to perform the testing, and associated examples.

What is Hypothesis Testing in Statistics?

Hypothesis testing uses sample data from the population to draw useful conclusions regarding the population probability distribution . It tests an assumption made about the data using different types of hypothesis testing methodologies. The hypothesis testing results in either rejecting or not rejecting the null hypothesis.

Hypothesis Testing Definition

Hypothesis testing can be defined as a statistical tool that is used to identify if the results of an experiment are meaningful or not. It involves setting up a null hypothesis and an alternative hypothesis. These two hypotheses will always be mutually exclusive. This means that if the null hypothesis is true then the alternative hypothesis is false and vice versa. An example of hypothesis testing is setting up a test to check if a new medicine works on a disease in a more efficient manner.

Null Hypothesis

The null hypothesis is a concise mathematical statement that is used to indicate that there is no difference between two possibilities. In other words, there is no difference between certain characteristics of data. This hypothesis assumes that the outcomes of an experiment are based on chance alone. It is denoted as \(H_{0}\). Hypothesis testing is used to conclude if the null hypothesis can be rejected or not. Suppose an experiment is conducted to check if girls are shorter than boys at the age of 5. The null hypothesis will say that they are the same height.

Alternative Hypothesis

The alternative hypothesis is an alternative to the null hypothesis. It is used to show that the observations of an experiment are due to some real effect. It indicates that there is a statistical significance between two possible outcomes and can be denoted as \(H_{1}\) or \(H_{a}\). For the above-mentioned example, the alternative hypothesis would be that girls are shorter than boys at the age of 5.

Hypothesis Testing P Value

In hypothesis testing, the p value is used to indicate whether the results obtained after conducting a test are statistically significant or not. It also indicates the probability of making an error in rejecting or not rejecting the null hypothesis.This value is always a number between 0 and 1. The p value is compared to an alpha level, \(\alpha\) or significance level. The alpha level can be defined as the acceptable risk of incorrectly rejecting the null hypothesis. The alpha level is usually chosen between 1% to 5%.

Hypothesis Testing Critical region

All sets of values that lead to rejecting the null hypothesis lie in the critical region. Furthermore, the value that separates the critical region from the non-critical region is known as the critical value.

Hypothesis Testing Formula

Depending upon the type of data available and the size, different types of hypothesis testing are used to determine whether the null hypothesis can be rejected or not. The hypothesis testing formula for some important test statistics are given below:

• z = \(\frac{\overline{x}-\mu}{\frac{\sigma}{\sqrt{n}}}\). \(\overline{x}\) is the sample mean, \(\mu\) is the population mean, \(\sigma\) is the population standard deviation and n is the size of the sample.
• t = \(\frac{\overline{x}-\mu}{\frac{s}{\sqrt{n}}}\). s is the sample standard deviation.
• \(\chi ^{2} = \sum \frac{(O_{i}-E_{i})^{2}}{E_{i}}\). \(O_{i}\) is the observed value and \(E_{i}\) is the expected value.

We will learn more about these test statistics in the upcoming section.

Types of Hypothesis Testing

Selecting the correct test for performing hypothesis testing can be confusing. These tests are used to determine a test statistic on the basis of which the null hypothesis can either be rejected or not rejected. Some of the important tests used for hypothesis testing are given below.

Hypothesis Testing Z Test

A z test is a way of hypothesis testing that is used for a large sample size (n ≥ 30). It is used to determine whether there is a difference between the population mean and the sample mean when the population standard deviation is known. It can also be used to compare the mean of two samples. It is used to compute the z test statistic. The formulas are given as follows:

• One sample: z = \(\frac{\overline{x}-\mu}{\frac{\sigma}{\sqrt{n}}}\).
• Two samples: z = \(\frac{(\overline{x_{1}}-\overline{x_{2}})-(\mu_{1}-\mu_{2})}{\sqrt{\frac{\sigma_{1}^{2}}{n_{1}}+\frac{\sigma_{2}^{2}}{n_{2}}}}\).

Hypothesis Testing t Test

The t test is another method of hypothesis testing that is used for a small sample size (n < 30). It is also used to compare the sample mean and population mean. However, the population standard deviation is not known. Instead, the sample standard deviation is known. The mean of two samples can also be compared using the t test.

• One sample: t = \(\frac{\overline{x}-\mu}{\frac{s}{\sqrt{n}}}\).
• Two samples: t = \(\frac{(\overline{x_{1}}-\overline{x_{2}})-(\mu_{1}-\mu_{2})}{\sqrt{\frac{s_{1}^{2}}{n_{1}}+\frac{s_{2}^{2}}{n_{2}}}}\).

Hypothesis Testing Chi Square

The Chi square test is a hypothesis testing method that is used to check whether the variables in a population are independent or not. It is used when the test statistic is chi-squared distributed.

One Tailed Hypothesis Testing

One tailed hypothesis testing is done when the rejection region is only in one direction. It can also be known as directional hypothesis testing because the effects can be tested in one direction only. This type of testing is further classified into the right tailed test and left tailed test.

Right Tailed Hypothesis Testing

The right tail test is also known as the upper tail test. This test is used to check whether the population parameter is greater than some value. The null and alternative hypotheses for this test are given as follows:

\(H_{0}\): The population parameter is ≤ some value

\(H_{1}\): The population parameter is > some value.

If the test statistic has a greater value than the critical value then the null hypothesis is rejected

Left Tailed Hypothesis Testing

The left tail test is also known as the lower tail test. It is used to check whether the population parameter is less than some value. The hypotheses for this hypothesis testing can be written as follows:

\(H_{0}\): The population parameter is ≥ some value

\(H_{1}\): The population parameter is < some value.

The null hypothesis is rejected if the test statistic has a value lesser than the critical value.

Two Tailed Hypothesis Testing

In this hypothesis testing method, the critical region lies on both sides of the sampling distribution. It is also known as a non - directional hypothesis testing method. The two-tailed test is used when it needs to be determined if the population parameter is assumed to be different than some value. The hypotheses can be set up as follows:

\(H_{0}\): the population parameter = some value

\(H_{1}\): the population parameter ≠ some value

The null hypothesis is rejected if the test statistic has a value that is not equal to the critical value.

Hypothesis Testing Steps

Hypothesis testing can be easily performed in five simple steps. The most important step is to correctly set up the hypotheses and identify the right method for hypothesis testing. The basic steps to perform hypothesis testing are as follows:

• Step 1: Set up the null hypothesis by correctly identifying whether it is the left-tailed, right-tailed, or two-tailed hypothesis testing.
• Step 2: Set up the alternative hypothesis.
• Step 3: Choose the correct significance level, \(\alpha\), and find the critical value.
• Step 4: Calculate the correct test statistic (z, t or \(\chi\)) and p-value.
• Step 5: Compare the test statistic with the critical value or compare the p-value with \(\alpha\) to arrive at a conclusion. In other words, decide if the null hypothesis is to be rejected or not.

Hypothesis Testing Example

The best way to solve a problem on hypothesis testing is by applying the 5 steps mentioned in the previous section. Suppose a researcher claims that the mean average weight of men is greater than 100kgs with a standard deviation of 15kgs. 30 men are chosen with an average weight of 112.5 Kgs. Using hypothesis testing, check if there is enough evidence to support the researcher's claim. The confidence interval is given as 95%.

Step 1: This is an example of a right-tailed test. Set up the null hypothesis as \(H_{0}\): \(\mu\) = 100.

Step 2: The alternative hypothesis is given by \(H_{1}\): \(\mu\) > 100.

Step 3: As this is a one-tailed test, \(\alpha\) = 100% - 95% = 5%. This can be used to determine the critical value.

1 - \(\alpha\) = 1 - 0.05 = 0.95

0.95 gives the required area under the curve. Now using a normal distribution table, the area 0.95 is at z = 1.645. A similar process can be followed for a t-test. The only additional requirement is to calculate the degrees of freedom given by n - 1.

Step 4: Calculate the z test statistic. This is because the sample size is 30. Furthermore, the sample and population means are known along with the standard deviation.

z = \(\frac{\overline{x}-\mu}{\frac{\sigma}{\sqrt{n}}}\).

\(\mu\) = 100, \(\overline{x}\) = 112.5, n = 30, \(\sigma\) = 15

z = \(\frac{112.5-100}{\frac{15}{\sqrt{30}}}\) = 4.56

Step 5: Conclusion. As 4.56 > 1.645 thus, the null hypothesis can be rejected.

Hypothesis Testing and Confidence Intervals

Confidence intervals form an important part of hypothesis testing. This is because the alpha level can be determined from a given confidence interval. Suppose a confidence interval is given as 95%. Subtract the confidence interval from 100%. This gives 100 - 95 = 5% or 0.05. This is the alpha value of a one-tailed hypothesis testing. To obtain the alpha value for a two-tailed hypothesis testing, divide this value by 2. This gives 0.05 / 2 = 0.025.

Related Articles:

• Probability and Statistics
• Data Handling

Important Notes on Hypothesis Testing

• Hypothesis testing is a technique that is used to verify whether the results of an experiment are statistically significant.
• It involves the setting up of a null hypothesis and an alternate hypothesis.
• There are three types of tests that can be conducted under hypothesis testing - z test, t test, and chi square test.
• Hypothesis testing can be classified as right tail, left tail, and two tail tests.

Examples on Hypothesis Testing

• Example 1: The average weight of a dumbbell in a gym is 90lbs. However, a physical trainer believes that the average weight might be higher. A random sample of 5 dumbbells with an average weight of 110lbs and a standard deviation of 18lbs. Using hypothesis testing check if the physical trainer's claim can be supported for a 95% confidence level. Solution: As the sample size is lesser than 30, the t-test is used. \(H_{0}\): \(\mu\) = 90, \(H_{1}\): \(\mu\) > 90 \(\overline{x}\) = 110, \(\mu\) = 90, n = 5, s = 18. \(\alpha\) = 0.05 Using the t-distribution table, the critical value is 2.132 t = \(\frac{\overline{x}-\mu}{\frac{s}{\sqrt{n}}}\) t = 2.484 As 2.484 > 2.132, the null hypothesis is rejected. Answer: The average weight of the dumbbells may be greater than 90lbs
• Example 2: The average score on a test is 80 with a standard deviation of 10. With a new teaching curriculum introduced it is believed that this score will change. On random testing, the score of 38 students, the mean was found to be 88. With a 0.05 significance level, is there any evidence to support this claim? Solution: This is an example of two-tail hypothesis testing. The z test will be used. \(H_{0}\): \(\mu\) = 80, \(H_{1}\): \(\mu\) ≠ 80 \(\overline{x}\) = 88, \(\mu\) = 80, n = 36, \(\sigma\) = 10. \(\alpha\) = 0.05 / 2 = 0.025 The critical value using the normal distribution table is 1.96 z = \(\frac{\overline{x}-\mu}{\frac{\sigma}{\sqrt{n}}}\) z = \(\frac{88-80}{\frac{10}{\sqrt{36}}}\) = 4.8 As 4.8 > 1.96, the null hypothesis is rejected. Answer: There is a difference in the scores after the new curriculum was introduced.
• Example 3: The average score of a class is 90. However, a teacher believes that the average score might be lower. The scores of 6 students were randomly measured. The mean was 82 with a standard deviation of 18. With a 0.05 significance level use hypothesis testing to check if this claim is true. Solution: The t test will be used. \(H_{0}\): \(\mu\) = 90, \(H_{1}\): \(\mu\) < 90 \(\overline{x}\) = 110, \(\mu\) = 90, n = 6, s = 18 The critical value from the t table is -2.015 t = \(\frac{\overline{x}-\mu}{\frac{s}{\sqrt{n}}}\) t = \(\frac{82-90}{\frac{18}{\sqrt{6}}}\) t = -1.088 As -1.088 > -2.015, we fail to reject the null hypothesis. Answer: There is not enough evidence to support the claim.

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FAQs on Hypothesis Testing

What is hypothesis testing.

Hypothesis testing in statistics is a tool that is used to make inferences about the population data. It is also used to check if the results of an experiment are valid.

What is the z Test in Hypothesis Testing?

The z test in hypothesis testing is used to find the z test statistic for normally distributed data . The z test is used when the standard deviation of the population is known and the sample size is greater than or equal to 30.

What is the t Test in Hypothesis Testing?

The t test in hypothesis testing is used when the data follows a student t distribution . It is used when the sample size is less than 30 and standard deviation of the population is not known.

What is the formula for z test in Hypothesis Testing?

The formula for a one sample z test in hypothesis testing is z = \(\frac{\overline{x}-\mu}{\frac{\sigma}{\sqrt{n}}}\) and for two samples is z = \(\frac{(\overline{x_{1}}-\overline{x_{2}})-(\mu_{1}-\mu_{2})}{\sqrt{\frac{\sigma_{1}^{2}}{n_{1}}+\frac{\sigma_{2}^{2}}{n_{2}}}}\).

What is the p Value in Hypothesis Testing?

The p value helps to determine if the test results are statistically significant or not. In hypothesis testing, the null hypothesis can either be rejected or not rejected based on the comparison between the p value and the alpha level.

What is One Tail Hypothesis Testing?

When the rejection region is only on one side of the distribution curve then it is known as one tail hypothesis testing. The right tail test and the left tail test are two types of directional hypothesis testing.

What is the Alpha Level in Two Tail Hypothesis Testing?

To get the alpha level in a two tail hypothesis testing divide \(\alpha\) by 2. This is done as there are two rejection regions in the curve.

• Hypothesis Testing: Definition, Uses, Limitations + Examples

Hypothesis testing is as old as the scientific method and is at the heart of the research process. 

Research exists to validate or disprove assumptions about various phenomena. The process of validation involves testing and it is in this context that we will explore hypothesis testing. 

What is a Hypothesis? 

A hypothesis is a calculated prediction or assumption about a population parameter based on limited evidence. The whole idea behind hypothesis formulation is testing—this means the researcher subjects his or her calculated assumption to a series of evaluations to know whether they are true or false. 

Typically, every research starts with a hypothesis—the investigator makes a claim and experiments to prove that this claim is true or false . For instance, if you predict that students who drink milk before class perform better than those who don’t, then this becomes a hypothesis that can be confirmed or refuted using an experiment.  

Read: What is Empirical Research Study? [Examples & Method]

What are the Types of Hypotheses? 

1. simple hypothesis.

Also known as a basic hypothesis, a simple hypothesis suggests that an independent variable is responsible for a corresponding dependent variable. In other words, an occurrence of the independent variable inevitably leads to an occurrence of the dependent variable. 

Typically, simple hypotheses are considered as generally true, and they establish a causal relationship between two variables. 

Examples of Simple Hypothesis  

• Drinking soda and other sugary drinks can cause obesity. 
• Smoking cigarettes daily leads to lung cancer.

2. Complex Hypothesis

A complex hypothesis is also known as a modal. It accounts for the causal relationship between two independent variables and the resulting dependent variables. This means that the combination of the independent variables leads to the occurrence of the dependent variables . 

Examples of Complex Hypotheses  

• Adults who do not smoke and drink are less likely to develop liver-related conditions.
• Global warming causes icebergs to melt which in turn causes major changes in weather patterns.

3. Null Hypothesis

As the name suggests, a null hypothesis is formed when a researcher suspects that there’s no relationship between the variables in an observation. In this case, the purpose of the research is to approve or disapprove this assumption. 

Examples of Null Hypothesis

• This is no significant change in a student’s performance if they drink coffee or tea before classes. 
• There’s no significant change in the growth of a plant if one uses distilled water only or vitamin-rich water. 

Read: Research Report: Definition, Types + [Writing Guide]

4. Alternative Hypothesis 

To disapprove a null hypothesis, the researcher has to come up with an opposite assumption—this assumption is known as the alternative hypothesis. This means if the null hypothesis says that A is false, the alternative hypothesis assumes that A is true. 

An alternative hypothesis can be directional or non-directional depending on the direction of the difference. A directional alternative hypothesis specifies the direction of the tested relationship, stating that one variable is predicted to be larger or smaller than the null value while a non-directional hypothesis only validates the existence of a difference without stating its direction. 

Examples of Alternative Hypotheses  

• Starting your day with a cup of tea instead of a cup of coffee can make you more alert in the morning. 
• The growth of a plant improves significantly when it receives distilled water instead of vitamin-rich water. 

5. Logical Hypothesis

Logical hypotheses are some of the most common types of calculated assumptions in systematic investigations. It is an attempt to use your reasoning to connect different pieces in research and build a theory using little evidence. In this case, the researcher uses any data available to him, to form a plausible assumption that can be tested. 

Examples of Logical Hypothesis

• Waking up early helps you to have a more productive day. 
• Beings from Mars would not be able to breathe the air in the atmosphere of the Earth. 

6. Empirical Hypothesis  

After forming a logical hypothesis, the next step is to create an empirical or working hypothesis. At this stage, your logical hypothesis undergoes systematic testing to prove or disprove the assumption. An empirical hypothesis is subject to several variables that can trigger changes and lead to specific outcomes. 

Examples of Empirical Testing 

• People who eat more fish run faster than people who eat meat.
• Women taking vitamin E grow hair faster than those taking vitamin K.

7. Statistical Hypothesis

When forming a statistical hypothesis, the researcher examines the portion of a population of interest and makes a calculated assumption based on the data from this sample. A statistical hypothesis is most common with systematic investigations involving a large target audience. Here, it’s impossible to collect responses from every member of the population so you have to depend on data from your sample and extrapolate the results to the wider population. 

Examples of Statistical Hypothesis  

• 45% of students in Louisiana have middle-income parents. 
• 80% of the UK’s population gets a divorce because of irreconcilable differences.

What is Hypothesis Testing? 

Hypothesis testing is an assessment method that allows researchers to determine the plausibility of a hypothesis. It involves testing an assumption about a specific population parameter to know whether it’s true or false. These population parameters include variance, standard deviation, and median. 

Typically, hypothesis testing starts with developing a null hypothesis and then performing several tests that support or reject the null hypothesis. The researcher uses test statistics to compare the association or relationship between two or more variables. 

Explore: Research Bias: Definition, Types + Examples

Researchers also use hypothesis testing to calculate the coefficient of variation and determine if the regression relationship and the correlation coefficient are statistically significant.

How Hypothesis Testing Works

The basis of hypothesis testing is to examine and analyze the null hypothesis and alternative hypothesis to know which one is the most plausible assumption. Since both assumptions are mutually exclusive, only one can be true. In other words, the occurrence of a null hypothesis destroys the chances of the alternative coming to life, and vice-versa. 

Interesting: 21 Chrome Extensions for Academic Researchers in 2021

What Are The Stages of Hypothesis Testing?  

To successfully confirm or refute an assumption, the researcher goes through five (5) stages of hypothesis testing; 

• Determine the null hypothesis
• Specify the alternative hypothesis
• Set the significance level
• Calculate the test statistics and corresponding P-value
• Draw your conclusion
• Determine the Null Hypothesis

Like we mentioned earlier, hypothesis testing starts with creating a null hypothesis which stands as an assumption that a certain statement is false or implausible. For example, the null hypothesis (H0) could suggest that different subgroups in the research population react to a variable in the same way. 

• Specify the Alternative Hypothesis

Once you know the variables for the null hypothesis, the next step is to determine the alternative hypothesis. The alternative hypothesis counters the null assumption by suggesting the statement or assertion is true. Depending on the purpose of your research, the alternative hypothesis can be one-sided or two-sided. 

Using the example we established earlier, the alternative hypothesis may argue that the different sub-groups react differently to the same variable based on several internal and external factors. 

• Set the Significance Level

Many researchers create a 5% allowance for accepting the value of an alternative hypothesis, even if the value is untrue. This means that there is a 0.05 chance that one would go with the value of the alternative hypothesis, despite the truth of the null hypothesis. 

Something to note here is that the smaller the significance level, the greater the burden of proof needed to reject the null hypothesis and support the alternative hypothesis.

Explore: What is Data Interpretation? + [Types, Method & Tools]

• Calculate the Test Statistics and Corresponding P-Value 

Test statistics in hypothesis testing allow you to compare different groups between variables while the p-value accounts for the probability of obtaining sample statistics if your null hypothesis is true. In this case, your test statistics can be the mean, median and similar parameters. 

If your p-value is 0.65, for example, then it means that the variable in your hypothesis will happen 65 in100 times by pure chance. Use this formula to determine the p-value for your data: 

• Draw Your Conclusions

After conducting a series of tests, you should be able to agree or refute the hypothesis based on feedback and insights from your sample data.  

Applications of Hypothesis Testing in Research

Hypothesis testing isn’t only confined to numbers and calculations; it also has several real-life applications in business, manufacturing, advertising, and medicine. 

In a factory or other manufacturing plants, hypothesis testing is an important part of quality and production control before the final products are approved and sent out to the consumer. 

During ideation and strategy development, C-level executives use hypothesis testing to evaluate their theories and assumptions before any form of implementation. For example, they could leverage hypothesis testing to determine whether or not some new advertising campaign, marketing technique, etc. causes increased sales. 

In addition, hypothesis testing is used during clinical trials to prove the efficacy of a drug or new medical method before its approval for widespread human usage. 

What is an Example of Hypothesis Testing?

An employer claims that her workers are of above-average intelligence. She takes a random sample of 20 of them and gets the following results: 

Mean IQ Scores: 110

Standard Deviation: 15 

Mean Population IQ: 100

Step 1: Using the value of the mean population IQ, we establish the null hypothesis as 100.

Step 2: State that the alternative hypothesis is greater than 100.

Step 3: State the alpha level as 0.05 or 5% 

Step 4: Find the rejection region area (given by your alpha level above) from the z-table. An area of .05 is equal to a z-score of 1.645.

Step 5: Calculate the test statistics using this formula

Z = (110–100) ÷ (15÷√20) 

10 ÷ 3.35 = 2.99 

If the value of the test statistics is higher than the value of the rejection region, then you should reject the null hypothesis. If it is less, then you cannot reject the null. 

In this case, 2.99 > 1.645 so we reject the null. 

Importance/Benefits of Hypothesis Testing 

The most significant benefit of hypothesis testing is it allows you to evaluate the strength of your claim or assumption before implementing it in your data set. Also, hypothesis testing is the only valid method to prove that something “is or is not”. Other benefits include: 

• Hypothesis testing provides a reliable framework for making any data decisions for your population of interest. 
• It helps the researcher to successfully extrapolate data from the sample to the larger population. 
• Hypothesis testing allows the researcher to determine whether the data from the sample is statistically significant. 
• Hypothesis testing is one of the most important processes for measuring the validity and reliability of outcomes in any systematic investigation. 
• It helps to provide links to the underlying theory and specific research questions.

Criticism and Limitations of Hypothesis Testing

Several limitations of hypothesis testing can affect the quality of data you get from this process. Some of these limitations include: 

• The interpretation of a p-value for observation depends on the stopping rule and definition of multiple comparisons. This makes it difficult to calculate since the stopping rule is subject to numerous interpretations, plus “multiple comparisons” are unavoidably ambiguous. 
• Conceptual issues often arise in hypothesis testing, especially if the researcher merges Fisher and Neyman-Pearson’s methods which are conceptually distinct. 
• In an attempt to focus on the statistical significance of the data, the researcher might ignore the estimation and confirmation by repeated experiments.
• Hypothesis testing can trigger publication bias, especially when it requires statistical significance as a criterion for publication.
• When used to detect whether a difference exists between groups, hypothesis testing can trigger absurd assumptions that affect the reliability of your observation.

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8.1: The Elements of Hypothesis Testing

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Learning Objectives

• To understand the logical framework of tests of hypotheses.
• To learn basic terminology connected with hypothesis testing.
• To learn fundamental facts about hypothesis testing.

Types of Hypotheses

A hypothesis about the value of a population parameter is an assertion about its value. As in the introductory example we will be concerned with testing the truth of two competing hypotheses, only one of which can be true.

Definition: null hypothesis and alternative hypothesis

• The null hypothesis , denoted \(H_0\), is the statement about the population parameter that is assumed to be true unless there is convincing evidence to the contrary.
• The alternative hypothesis , denoted \(H_a\), is a statement about the population parameter that is contradictory to the null hypothesis, and is accepted as true only if there is convincing evidence in favor of it.

Definition: statistical procedure

Hypothesis testing is a statistical procedure in which a choice is made between a null hypothesis and an alternative hypothesis based on information in a sample.

The end result of a hypotheses testing procedure is a choice of one of the following two possible conclusions:

• Reject \(H_0\) (and therefore accept \(H_a\)), or
• Fail to reject \(H_0\) (and therefore fail to accept \(H_a\)).

The null hypothesis typically represents the status quo, or what has historically been true. In the example of the respirators, we would believe the claim of the manufacturer unless there is reason not to do so, so the null hypotheses is \(H_0:\mu =75\). The alternative hypothesis in the example is the contradictory statement \(H_a:\mu <75\). The null hypothesis will always be an assertion containing an equals sign, but depending on the situation the alternative hypothesis can have any one of three forms: with the symbol \(<\), as in the example just discussed, with the symbol \(>\), or with the symbol \(\neq\). The following two examples illustrate the latter two cases.

Example \(\PageIndex{1}\)

A publisher of college textbooks claims that the average price of all hardbound college textbooks is \(\$127.50\). A student group believes that the actual mean is higher and wishes to test their belief. State the relevant null and alternative hypotheses.

The default option is to accept the publisher’s claim unless there is compelling evidence to the contrary. Thus the null hypothesis is \(H_0:\mu =127.50\). Since the student group thinks that the average textbook price is greater than the publisher’s figure, the alternative hypothesis in this situation is \(H_a:\mu >127.50\).

Example \(\PageIndex{2}\)

The recipe for a bakery item is designed to result in a product that contains \(8\) grams of fat per serving. The quality control department samples the product periodically to insure that the production process is working as designed. State the relevant null and alternative hypotheses.

The default option is to assume that the product contains the amount of fat it was formulated to contain unless there is compelling evidence to the contrary. Thus the null hypothesis is \(H_0:\mu =8.0\). Since to contain either more fat than desired or to contain less fat than desired are both an indication of a faulty production process, the alternative hypothesis in this situation is that the mean is different from \(8.0\), so \(H_a:\mu \neq 8.0\).

In Example \(\PageIndex{1}\), the textbook example, it might seem more natural that the publisher’s claim be that the average price is at most \(\$127.50\), not exactly \(\$127.50\). If the claim were made this way, then the null hypothesis would be \(H_0:\mu \leq 127.50\), and the value \(\$127.50\) given in the example would be the one that is least favorable to the publisher’s claim, the null hypothesis. It is always true that if the null hypothesis is retained for its least favorable value, then it is retained for every other value.

Thus in order to make the null and alternative hypotheses easy for the student to distinguish, in every example and problem in this text we will always present one of the two competing claims about the value of a parameter with an equality. The claim expressed with an equality is the null hypothesis. This is the same as always stating the null hypothesis in the least favorable light. So in the introductory example about the respirators, we stated the manufacturer’s claim as “the average is \(75\) minutes” instead of the perhaps more natural “the average is at least \(75\) minutes,” essentially reducing the presentation of the null hypothesis to its worst case.

The first step in hypothesis testing is to identify the null and alternative hypotheses.

The Logic of Hypothesis Testing

Although we will study hypothesis testing in situations other than for a single population mean (for example, for a population proportion instead of a mean or in comparing the means of two different populations), in this section the discussion will always be given in terms of a single population mean \(\mu\).

The null hypothesis always has the form \(H_0:\mu =\mu _0\) for a specific number \(\mu _0\) (in the respirator example \(\mu _0=75\), in the textbook example \(\mu _0=127.50\), and in the baked goods example \(\mu _0=8.0\)). Since the null hypothesis is accepted unless there is strong evidence to the contrary, the test procedure is based on the initial assumption that \(H_0\) is true. This point is so important that we will repeat it in a display:

The test procedure is based on the initial assumption that \(H_0\) is true.

The criterion for judging between \(H_0\) and \(H_a\) based on the sample data is: if the value of \(\overline{X}\) would be highly unlikely to occur if \(H_0\) were true, but favors the truth of \(H_a\), then we reject \(H_0\) in favor of \(H_a\). Otherwise we do not reject \(H_0\).

Supposing for now that \(\overline{X}\) follows a normal distribution, when the null hypothesis is true the density function for the sample mean \(\overline{X}\) must be as in Figure \(\PageIndex{1}\): a bell curve centered at \(\mu _0\). Thus if \(H_0\) is true then \(\overline{X}\) is likely to take a value near \(\mu _0\) and is unlikely to take values far away. Our decision procedure therefore reduces simply to:

• if \(H_a\) has the form \(H_a:\mu <\mu _0\) then reject \(H_0\) if \(\bar{x}\) is far to the left of \(\mu _0\);
• if \(H_a\) has the form \(H_a:\mu >\mu _0\) then reject \(H_0\) if \(\bar{x}\) is far to the right of \(\mu _0\);
• if \(H_a\) has the form \(H_a:\mu \neq \mu _0\) then reject \(H_0\) if \(\bar{x}\) is far away from \(\mu _0\) in either direction.

Think of the respirator example, for which the null hypothesis is \(H_0:\mu =75\), the claim that the average time air is delivered for all respirators is \(75\) minutes. If the sample mean is \(75\) or greater then we certainly would not reject \(H_0\) (since there is no issue with an emergency respirator delivering air even longer than claimed).

If the sample mean is slightly less than \(75\) then we would logically attribute the difference to sampling error and also not reject \(H_0\) either.

Values of the sample mean that are smaller and smaller are less and less likely to come from a population for which the population mean is \(75\). Thus if the sample mean is far less than \(75\), say around \(60\) minutes or less, then we would certainly reject \(H_0\), because we know that it is highly unlikely that the average of a sample would be so low if the population mean were \(75\). This is the rare event criterion for rejection: what we actually observed \((\overline{X}<60)\) would be so rare an event if \(\mu =75\) were true that we regard it as much more likely that the alternative hypothesis \(\mu <75\) holds.

In summary, to decide between \(H_0\) and \(H_a\) in this example we would select a “rejection region” of values sufficiently far to the left of \(75\), based on the rare event criterion, and reject \(H_0\) if the sample mean \(\overline{X}\) lies in the rejection region, but not reject \(H_0\) if it does not.

The Rejection Region

Each different form of the alternative hypothesis Ha has its own kind of rejection region:

• if (as in the respirator example) \(H_a\) has the form \(H_a:\mu <\mu _0\), we reject \(H_0\) if \(\bar{x}\) is far to the left of \(\mu _0\), that is, to the left of some number \(C\), so the rejection region has the form of an interval \((-\infty ,C]\);
• if (as in the textbook example) \(H_a\) has the form \(H_a:\mu >\mu _0\), we reject \(H_0\) if \(\bar{x}\) is far to the right of \(\mu _0\), that is, to the right of some number \(C\), so the rejection region has the form of an interval \([C,\infty )\);
• if (as in the baked good example) \(H_a\) has the form \(H_a:\mu \neq \mu _0\), we reject \(H_0\) if \(\bar{x}\) is far away from \(\mu _0\) in either direction, that is, either to the left of some number \(C\) or to the right of some other number \(C′\), so the rejection region has the form of the union of two intervals \((-\infty ,C]\cup [C',\infty )\).

The key issue in our line of reasoning is the question of how to determine the number \(C\) or numbers \(C\) and \(C′\), called the critical value or critical values of the statistic, that determine the rejection region.

Definition: critical values

The critical value or critical values of a test of hypotheses are the number or numbers that determine the rejection region.

Suppose the rejection region is a single interval, so we need to select a single number \(C\). Here is the procedure for doing so. We select a small probability, denoted \(\alpha\), say \(1\%\), which we take as our definition of “rare event:” an event is “rare” if its probability of occurrence is less than \(\alpha\). (In all the examples and problems in this text the value of \(\alpha\) will be given already.) The probability that \(\overline{X}\) takes a value in an interval is the area under its density curve and above that interval, so as shown in Figure \(\PageIndex{2}\) (drawn under the assumption that \(H_0\) is true, so that the curve centers at \(\mu _0\)) the critical value \(C\) is the value of \(\overline{X}\) that cuts off a tail area \(\alpha\) in the probability density curve of \(\overline{X}\). When the rejection region is in two pieces, that is, composed of two intervals, the total area above both of them must be \(\alpha\), so the area above each one is \(\alpha /2\), as also shown in Figure \(\PageIndex{2}\).

The number \(\alpha\) is the total area of a tail or a pair of tails.

Example \(\PageIndex{3}\)

In the context of Example \(\PageIndex{2}\), suppose that it is known that the population is normally distributed with standard deviation \(\alpha =0.15\) gram, and suppose that the test of hypotheses \(H_0:\mu =8.0\) versus \(H_a:\mu \neq 8.0\) will be performed with a sample of size \(5\). Construct the rejection region for the test for the choice \(\alpha =0.10\). Explain the decision procedure and interpret it.

If \(H_0\) is true then the sample mean \(\overline{X}\) is normally distributed with mean and standard deviation

\[\begin{align} \mu _{\overline{X}} &=\mu \nonumber \\[5pt] &=8.0 \nonumber \end{align} \nonumber \]

\[\begin{align} \sigma _{\overline{X}}&=\dfrac{\sigma}{\sqrt{n}} \nonumber \\[5pt] &= \dfrac{0.15}{\sqrt{5}} \nonumber\\[5pt] &=0.067 \nonumber \end{align} \nonumber \]

Since \(H_a\) contains the \(\neq\) symbol the rejection region will be in two pieces, each one corresponding to a tail of area \(\alpha /2=0.10/2=0.05\). From Figure 7.1.6, \(z_{0.05}=1.645\), so \(C\) and \(C′\) are \(1.645\) standard deviations of \(\overline{X}\) to the right and left of its mean \(8.0\):

\[C=8.0-(1.645)(0.067) = 7.89 \; \; \text{and}\; \; C'=8.0 + (1.645)(0.067) = 8.11 \nonumber \]

The result is shown in Figure \(\PageIndex{3}\). α = 0.1

The decision procedure is: take a sample of size \(5\) and compute the sample mean \(\bar{x}\). If \(\bar{x}\) is either \(7.89\) grams or less or \(8.11\) grams or more then reject the hypothesis that the average amount of fat in all servings of the product is \(8.0\) grams in favor of the alternative that it is different from \(8.0\) grams. Otherwise do not reject the hypothesis that the average amount is \(8.0\) grams.

The reasoning is that if the true average amount of fat per serving were \(8.0\) grams then there would be less than a \(10\%\) chance that a sample of size \(5\) would produce a mean of either \(7.89\) grams or less or \(8.11\) grams or more. Hence if that happened it would be more likely that the value \(8.0\) is incorrect (always assuming that the population standard deviation is \(0.15\) gram).

Because the rejection regions are computed based on areas in tails of distributions, as shown in Figure \(\PageIndex{2}\), hypothesis tests are classified according to the form of the alternative hypothesis in the following way.

Definitions: Test classifications

• If \(H_a\) has the form \(\mu \neq \mu _0\) the test is called a two-tailed test .
• If \(H_a\) has the form \(\mu < \mu _0\) the test is called a left-tailed test .
• If \(H_a\) has the form \(\mu > \mu _0\)the test is called a right-tailed test .

Each of the last two forms is also called a one-tailed test .

Two Types of Errors

The format of the testing procedure in general terms is to take a sample and use the information it contains to come to a decision about the two hypotheses. As stated before our decision will always be either

• reject the null hypothesis \(H_0\) in favor of the alternative \(H_a\) presented, or
• do not reject the null hypothesis \(H_0\) in favor of the alternative \(H_0\) presented.

There are four possible outcomes of hypothesis testing procedure, as shown in the following table:

As the table shows, there are two ways to be right and two ways to be wrong. Typically to reject \(H_0\) when it is actually true is a more serious error than to fail to reject it when it is false, so the former error is labeled “ Type I ” and the latter error “ Type II ”.

Definition: Type I and Type II errors

In a test of hypotheses:

• A Type I error is the decision to reject \(H_0\) when it is in fact true.
• A Type II error is the decision not to reject \(H_0\) when it is in fact not true.

Unless we perform a census we do not have certain knowledge, so we do not know whether our decision matches the true state of nature or if we have made an error. We reject \(H_0\) if what we observe would be a “rare” event if \(H_0\) were true. But rare events are not impossible: they occur with probability \(\alpha\). Thus when \(H_0\) is true, a rare event will be observed in the proportion \(\alpha\) of repeated similar tests, and \(H_0\) will be erroneously rejected in those tests. Thus \(\alpha\) is the probability that in following the testing procedure to decide between \(H_0\) and \(H_a\) we will make a Type I error.

Definition: level of significance

The number \(\alpha\) that is used to determine the rejection region is called the level of significance of the test. It is the probability that the test procedure will result in a Type I error .

The probability of making a Type II error is too complicated to discuss in a beginning text, so we will say no more about it than this: for a fixed sample size, choosing \(alpha\) smaller in order to reduce the chance of making a Type I error has the effect of increasing the chance of making a Type II error . The only way to simultaneously reduce the chances of making either kind of error is to increase the sample size.

Standardizing the Test Statistic

Hypotheses testing will be considered in a number of contexts, and great unification as well as simplification results when the relevant sample statistic is standardized by subtracting its mean from it and then dividing by its standard deviation. The resulting statistic is called a standardized test statistic . In every situation treated in this and the following two chapters the standardized test statistic will have either the standard normal distribution or Student’s \(t\)-distribution.

Definition: hypothesis test

A standardized test statistic for a hypothesis test is the statistic that is formed by subtracting from the statistic of interest its mean and dividing by its standard deviation.

For example, reviewing Example \(\PageIndex{3}\), if instead of working with the sample mean \(\overline{X}\) we instead work with the test statistic

\[\frac{\overline{X}-8.0}{0.067} \nonumber \]

then the distribution involved is standard normal and the critical values are just \(\pm z_{0.05}\). The extra work that was done to find that \(C=7.89\) and \(C′=8.11\) is eliminated. In every hypothesis test in this book the standardized test statistic will be governed by either the standard normal distribution or Student’s \(t\)-distribution. Information about rejection regions is summarized in the following tables:

Every instance of hypothesis testing discussed in this and the following two chapters will have a rejection region like one of the six forms tabulated in the tables above.

No matter what the context a test of hypotheses can always be performed by applying the following systematic procedure, which will be illustrated in the examples in the succeeding sections.

Systematic Hypothesis Testing Procedure: Critical Value Approach

• Identify the null and alternative hypotheses.
• Identify the relevant test statistic and its distribution.
• Compute from the data the value of the test statistic.
• Construct the rejection region.
• Compare the value computed in Step 3 to the rejection region constructed in Step 4 and make a decision. Formulate the decision in the context of the problem, if applicable.

The procedure that we have outlined in this section is called the “Critical Value Approach” to hypothesis testing to distinguish it from an alternative but equivalent approach that will be introduced at the end of Section 8.3.

Key Takeaway

• A test of hypotheses is a statistical process for deciding between two competing assertions about a population parameter.
• The testing procedure is formalized in a five-step procedure.

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StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-.

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Hypothesis testing, p values, confidence intervals, and significance.

Jacob Shreffler ; Martin R. Huecker .

Affiliations

Last Update: March 13, 2023 .

• Definition/Introduction

Medical providers often rely on evidence-based medicine to guide decision-making in practice. Often a research hypothesis is tested with results provided, typically with p values, confidence intervals, or both. Additionally, statistical or research significance is estimated or determined by the investigators. Unfortunately, healthcare providers may have different comfort levels in interpreting these findings, which may affect the adequate application of the data.

• Issues of Concern

Without a foundational understanding of hypothesis testing, p values, confidence intervals, and the difference between statistical and clinical significance, it may affect healthcare providers' ability to make clinical decisions without relying purely on the research investigators deemed level of significance. Therefore, an overview of these concepts is provided to allow medical professionals to use their expertise to determine if results are reported sufficiently and if the study outcomes are clinically appropriate to be applied in healthcare practice.

Hypothesis Testing

Investigators conducting studies need research questions and hypotheses to guide analyses. Starting with broad research questions (RQs), investigators then identify a gap in current clinical practice or research. Any research problem or statement is grounded in a better understanding of relationships between two or more variables. For this article, we will use the following research question example:

Research Question: Is Drug 23 an effective treatment for Disease A?

Research questions do not directly imply specific guesses or predictions; we must formulate research hypotheses. A hypothesis is a predetermined declaration regarding the research question in which the investigator(s) makes a precise, educated guess about a study outcome. This is sometimes called the alternative hypothesis and ultimately allows the researcher to take a stance based on experience or insight from medical literature. An example of a hypothesis is below.

Research Hypothesis: Drug 23 will significantly reduce symptoms associated with Disease A compared to Drug 22.

The null hypothesis states that there is no statistical difference between groups based on the stated research hypothesis.

Researchers should be aware of journal recommendations when considering how to report p values, and manuscripts should remain internally consistent.

Regarding p values, as the number of individuals enrolled in a study (the sample size) increases, the likelihood of finding a statistically significant effect increases. With very large sample sizes, the p-value can be very low significant differences in the reduction of symptoms for Disease A between Drug 23 and Drug 22. The null hypothesis is deemed true until a study presents significant data to support rejecting the null hypothesis. Based on the results, the investigators will either reject the null hypothesis (if they found significant differences or associations) or fail to reject the null hypothesis (they could not provide proof that there were significant differences or associations).

To test a hypothesis, researchers obtain data on a representative sample to determine whether to reject or fail to reject a null hypothesis. In most research studies, it is not feasible to obtain data for an entire population. Using a sampling procedure allows for statistical inference, though this involves a certain possibility of error. [1]  When determining whether to reject or fail to reject the null hypothesis, mistakes can be made: Type I and Type II errors. Though it is impossible to ensure that these errors have not occurred, researchers should limit the possibilities of these faults. [2]

Significance

Significance is a term to describe the substantive importance of medical research. Statistical significance is the likelihood of results due to chance. [3]  Healthcare providers should always delineate statistical significance from clinical significance, a common error when reviewing biomedical research. [4]  When conceptualizing findings reported as either significant or not significant, healthcare providers should not simply accept researchers' results or conclusions without considering the clinical significance. Healthcare professionals should consider the clinical importance of findings and understand both p values and confidence intervals so they do not have to rely on the researchers to determine the level of significance. [5]  One criterion often used to determine statistical significance is the utilization of p values.

P values are used in research to determine whether the sample estimate is significantly different from a hypothesized value. The p-value is the probability that the observed effect within the study would have occurred by chance if, in reality, there was no true effect. Conventionally, data yielding a p<0.05 or p<0.01 is considered statistically significant. While some have debated that the 0.05 level should be lowered, it is still universally practiced. [6]  Hypothesis testing allows us to determine the size of the effect.

An example of findings reported with p values are below:

Statement: Drug 23 reduced patients' symptoms compared to Drug 22. Patients who received Drug 23 (n=100) were 2.1 times less likely than patients who received Drug 22 (n = 100) to experience symptoms of Disease A, p<0.05.

Statement:Individuals who were prescribed Drug 23 experienced fewer symptoms (M = 1.3, SD = 0.7) compared to individuals who were prescribed Drug 22 (M = 5.3, SD = 1.9). This finding was statistically significant, p= 0.02.

For either statement, if the threshold had been set at 0.05, the null hypothesis (that there was no relationship) should be rejected, and we should conclude significant differences. Noticeably, as can be seen in the two statements above, some researchers will report findings with < or > and others will provide an exact p-value (0.000001) but never zero [6] . When examining research, readers should understand how p values are reported. The best practice is to report all p values for all variables within a study design, rather than only providing p values for variables with significant findings. [7]  The inclusion of all p values provides evidence for study validity and limits suspicion for selective reporting/data mining.  

While researchers have historically used p values, experts who find p values problematic encourage the use of confidence intervals. [8] . P-values alone do not allow us to understand the size or the extent of the differences or associations. [3]  In March 2016, the American Statistical Association (ASA) released a statement on p values, noting that scientific decision-making and conclusions should not be based on a fixed p-value threshold (e.g., 0.05). They recommend focusing on the significance of results in the context of study design, quality of measurements, and validity of data. Ultimately, the ASA statement noted that in isolation, a p-value does not provide strong evidence. [9]

When conceptualizing clinical work, healthcare professionals should consider p values with a concurrent appraisal study design validity. For example, a p-value from a double-blinded randomized clinical trial (designed to minimize bias) should be weighted higher than one from a retrospective observational study [7] . The p-value debate has smoldered since the 1950s [10] , and replacement with confidence intervals has been suggested since the 1980s. [11]

Confidence Intervals

A confidence interval provides a range of values within given confidence (e.g., 95%), including the accurate value of the statistical constraint within a targeted population. [12]  Most research uses a 95% CI, but investigators can set any level (e.g., 90% CI, 99% CI). [13]  A CI provides a range with the lower bound and upper bound limits of a difference or association that would be plausible for a population. [14]  Therefore, a CI of 95% indicates that if a study were to be carried out 100 times, the range would contain the true value in 95, [15]  confidence intervals provide more evidence regarding the precision of an estimate compared to p-values. [6]

In consideration of the similar research example provided above, one could make the following statement with 95% CI:

Statement: Individuals who were prescribed Drug 23 had no symptoms after three days, which was significantly faster than those prescribed Drug 22; there was a mean difference between the two groups of days to the recovery of 4.2 days (95% CI: 1.9 – 7.8).

It is important to note that the width of the CI is affected by the standard error and the sample size; reducing a study sample number will result in less precision of the CI (increase the width). [14]  A larger width indicates a smaller sample size or a larger variability. [16]  A researcher would want to increase the precision of the CI. For example, a 95% CI of 1.43 – 1.47 is much more precise than the one provided in the example above. In research and clinical practice, CIs provide valuable information on whether the interval includes or excludes any clinically significant values. [14]

Null values are sometimes used for differences with CI (zero for differential comparisons and 1 for ratios). However, CIs provide more information than that. [15]  Consider this example: A hospital implements a new protocol that reduced wait time for patients in the emergency department by an average of 25 minutes (95% CI: -2.5 – 41 minutes). Because the range crosses zero, implementing this protocol in different populations could result in longer wait times; however, the range is much higher on the positive side. Thus, while the p-value used to detect statistical significance for this may result in "not significant" findings, individuals should examine this range, consider the study design, and weigh whether or not it is still worth piloting in their workplace.

Similarly to p-values, 95% CIs cannot control for researchers' errors (e.g., study bias or improper data analysis). [14]  In consideration of whether to report p-values or CIs, researchers should examine journal preferences. When in doubt, reporting both may be beneficial. [13]  An example is below:

Reporting both: Individuals who were prescribed Drug 23 had no symptoms after three days, which was significantly faster than those prescribed Drug 22, p = 0.009. There was a mean difference between the two groups of days to the recovery of 4.2 days (95% CI: 1.9 – 7.8).

• Clinical Significance

Recall that clinical significance and statistical significance are two different concepts. Healthcare providers should remember that a study with statistically significant differences and large sample size may be of no interest to clinicians, whereas a study with smaller sample size and statistically non-significant results could impact clinical practice. [14]  Additionally, as previously mentioned, a non-significant finding may reflect the study design itself rather than relationships between variables.

Healthcare providers using evidence-based medicine to inform practice should use clinical judgment to determine the practical importance of studies through careful evaluation of the design, sample size, power, likelihood of type I and type II errors, data analysis, and reporting of statistical findings (p values, 95% CI or both). [4]  Interestingly, some experts have called for "statistically significant" or "not significant" to be excluded from work as statistical significance never has and will never be equivalent to clinical significance. [17]

The decision on what is clinically significant can be challenging, depending on the providers' experience and especially the severity of the disease. Providers should use their knowledge and experiences to determine the meaningfulness of study results and make inferences based not only on significant or insignificant results by researchers but through their understanding of study limitations and practical implications.

• Nursing, Allied Health, and Interprofessional Team Interventions

All physicians, nurses, pharmacists, and other healthcare professionals should strive to understand the concepts in this chapter. These individuals should maintain the ability to review and incorporate new literature for evidence-based and safe care. 

• Review Questions
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• Comment on this article.

Disclosure: Jacob Shreffler declares no relevant financial relationships with ineligible companies.

Disclosure: Martin Huecker declares no relevant financial relationships with ineligible companies.

This book is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits others to distribute the work, provided that the article is not altered or used commercially. You are not required to obtain permission to distribute this article, provided that you credit the author and journal.

• Cite this Page Shreffler J, Huecker MR. Hypothesis Testing, P Values, Confidence Intervals, and Significance. [Updated 2023 Mar 13]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-.

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• Knowledge Base

Test statistics | Definition, Interpretation, and Examples

Published on July 17, 2020 by Rebecca Bevans . Revised on June 22, 2023.

The test statistic is a number calculated from a statistical test of a hypothesis. It shows how closely your observed data match the distribution expected under the null hypothesis of that statistical test.

The test statistic is used to calculate the p value of your results, helping to decide whether to reject your null hypothesis.

Table of contents

What exactly is a test statistic, types of test statistics, interpreting test statistics, reporting test statistics, other interesting articles, frequently asked questions about test statistics.

A test statistic describes how closely the distribution of your data matches the distribution predicted under the null hypothesis of the statistical test you are using.

The distribution of data is how often each observation occurs, and can be described by its central tendency and variation around that central tendency. Different statistical tests predict different types of distributions, so it’s important to choose the right statistical test for your hypothesis.

The test statistic summarizes your observed data into a single number using the central tendency, variation, sample size, and number of predictor variables in your statistical model.

Generally, the test statistic is calculated as the pattern in your data (i.e., the correlation between variables or difference between groups) divided by the variance in the data (i.e., the standard deviation ).

• Null hypothesis ( H 0 ): There is no correlation between temperature and flowering date.
• Alternate hypothesis ( H A or H 1 ): There is a correlation between temperature and flowering date.

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Below is a summary of the most common test statistics, their hypotheses, and the types of statistical tests that use them.

Different statistical tests will have slightly different ways of calculating these test statistics, but the underlying hypotheses and interpretations of the test statistic stay the same.

In practice, you will almost always calculate your test statistic using a statistical program (R, SPSS, Excel, etc.), which will also calculate the p value of the test statistic. However, formulas to calculate these statistics by hand can be found online.

• a regression coefficient of 0.36
• a t value comparing that coefficient to the predicted range of regression coefficients under the null hypothesis of no relationship

The t value of the regression test is 2.36 – this is your test statistic.

For any combination of sample sizes and number of predictor variables, a statistical test will produce a predicted distribution for the test statistic. This shows the most likely range of values that will occur if your data follows the null hypothesis of the statistical test.

The more extreme your test statistic – the further to the edge of the range of predicted test values it is – the less likely it is that your data could have been generated under the null hypothesis of that statistical test.

The agreement between your calculated test statistic and the predicted values is described by the p value . The smaller the p value, the less likely your test statistic is to have occurred under the null hypothesis of the statistical test.

Because the test statistic is generated from your observed data, this ultimately means that the smaller the p value, the less likely it is that your data could have occurred if the null hypothesis was true.

Test statistics can be reported in the results section of your research paper along with the sample size, p value of the test, and any characteristics of your data that will help to put these results into context.

Whether or not you need to report the test statistic depends on the type of test you are reporting.

By surveying a random subset of 100 trees over 25 years we found a statistically significant ( p < 0.01) positive correlation between temperature and flowering dates ( R 2 = 0.36, SD = 0.057).

In our comparison of mouse diet A and mouse diet B, we found that the lifespan on diet A  ( M = 2.1 years; SD = 0.12) was significantly shorter than the lifespan on diet B ( M = 2.6 years; SD = 0.1), with an average difference of 6 months ( t (80) = -12.75; p < 0.01).

If you want to know more about statistics , methodology , or research bias , make sure to check out some of our other articles with explanations and examples.

• Confidence interval
• Descriptive statistics
• Measures of central tendency
• Correlation coefficient

Methodology

• Cluster sampling
• Stratified sampling
• Types of interviews
• Cohort study
• Thematic analysis

Research bias

• Implicit bias
• Cognitive bias
• Survivorship bias
• Availability heuristic
• Nonresponse bias
• Regression to the mean

A test statistic is a number calculated by a  statistical test . It describes how far your observed data is from the  null hypothesis  of no relationship between  variables or no difference among sample groups.

The test statistic tells you how different two or more groups are from the overall population mean , or how different a linear slope is from the slope predicted by a null hypothesis . Different test statistics are used in different statistical tests.

The formula for the test statistic depends on the statistical test being used.

Generally, the test statistic is calculated as the pattern in your data (i.e. the correlation between variables or difference between groups) divided by the variance in the data (i.e. the standard deviation ).

The test statistic you use will be determined by the statistical test.

You can choose the right statistical test by looking at what type of data you have collected and what type of relationship you want to test.

The test statistic will change based on the number of observations in your data, how variable your observations are, and how strong the underlying patterns in the data are.

For example, if one data set has higher variability while another has lower variability, the first data set will produce a test statistic closer to the null hypothesis , even if the true correlation between two variables is the same in either data set.

Statistical significance is a term used by researchers to state that it is unlikely their observations could have occurred under the null hypothesis of a statistical test . Significance is usually denoted by a p -value , or probability value.

Statistical significance is arbitrary – it depends on the threshold, or alpha value, chosen by the researcher. The most common threshold is p < 0.05, which means that the data is likely to occur less than 5% of the time under the null hypothesis .

When the p -value falls below the chosen alpha value, then we say the result of the test is statistically significant.

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• Statistical hypothesis testing

Definition Statistical hypothesis testing

Statistical hypothesis testing (also 'confirmatory data analysis') is used in inferential statistics to either confirm or falsify a hypothesis  based on empirical observations .

An example: It is assumed, that  people in the US, over time, are getting older (on average). In this case, the hypothesis to be confirmed is: 'the  average age of people in the US is rising'. This is called the alternative hypothesis , whereas the current opinion 'the average age of people in the US stays the same' is called the null hypothesis . The goal of a statistical test would be to either verify of falsify the alternative hypothesis.

In hypothesis testing, we differentiate between parametric and non-parametric tests. In parametric tests we compare location  and dispersion parameters of two samples and check for compliance. Examples for parametric tests are the t-test ,  f-test  and the χ2-test. In nonparametric tests on the other hand, no assumptions about probability distributions of the population which is being assessed are being made. Examples are the  Kolmogorov-Smirnov test, the chi-square test and the  Shapiro-Wilk test.

Performing hypothesis tests: In order to perform statistical hypothesis testing, we first have to collect the according empirical data  (for example: age reached of 100 people, born in 1900 and 1920 respectively). Depending on the hypothesis made and the resulting test procedure, a mathematically defined test statistic (f-statistic, t-statistic, …) is deducted from the observed data. Based on this value, we can determine whether the null hypothesis can be rejected or not – accounting for a specified rate of reliability (1- error probability). The null hypothesis should only be rejected based on a very low probability of error (p≤5%). Since errors when verifying or falsifying hypotheses cannot be generally excluded, errors of the first kind (=a true null hypothesis is incorrectly rejected, also: type I error) and errors of the second kind (= a true alternative hypothesis is incorrectly rejected, also: type II errors) are usually explicitly specified.

Please note that the definitions in our statistics encyclopedia are simplified explanations of terms. Our goal is to make the definitions accessible for a broad audience; thus it is possible that some definitions do not adhere entirely to scientific standards.

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Descriptive statistics, inferential statistics, stat reference, statistics - hypothesis testing.

Hypothesis testing is a formal way of checking if a hypothesis about a population is true or not.

Hypothesis Testing

A hypothesis is a claim about a population parameter .

A hypothesis test is a formal procedure to check if a hypothesis is true or not.

Examples of claims that can be checked:

The average height of people in Denmark is more than 170 cm.

The share of left handed people in Australia is not 10%.

The average income of dentists is less the average income of lawyers.

The Null and Alternative Hypothesis

Hypothesis testing is based on making two different claims about a population parameter.

The null hypothesis (\(H_{0} \)) and the alternative hypothesis (\(H_{1}\)) are the claims.

The two claims needs to be mutually exclusive , meaning only one of them can be true.

The alternative hypothesis is typically what we are trying to prove.

For example, we want to check the following claim:

"The average height of people in Denmark is more than 170 cm."

In this case, the parameter is the average height of people in Denmark (\(\mu\)).

The null and alternative hypothesis would be:

Null hypothesis : The average height of people in Denmark is 170 cm.

Alternative hypothesis : The average height of people in Denmark is more than 170 cm.

The claims are often expressed with symbols like this:

\(H_{0}\): \(\mu = 170 \: cm \)

\(H_{1}\): \(\mu > 170 \: cm \)

If the data supports the alternative hypothesis, we reject the null hypothesis and accept the alternative hypothesis.

If the data does not support the alternative hypothesis, we keep the null hypothesis.

Note: The alternative hypothesis is also referred to as (\(H_{A} \)).

The Significance Level

The significance level (\(\alpha\)) is the uncertainty we accept when rejecting the null hypothesis in the hypothesis test.

The significance level is a percentage probability of accidentally making the wrong conclusion.

Typical significance levels are:

• \(\alpha = 0.1\) (10%)
• \(\alpha = 0.05\) (5%)
• \(\alpha = 0.01\) (1%)

A lower significance level means that the evidence in the data needs to be stronger to reject the null hypothesis.

There is no "correct" significance level - it only states the uncertainty of the conclusion.

Note: A 5% significance level means that when we reject a null hypothesis:

We expect to reject a true null hypothesis 5 out of 100 times.

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The Test Statistic

The test statistic is used to decide the outcome of the hypothesis test.

The test statistic is a standardized value calculated from the sample.

Standardization means converting a statistic to a well known probability distribution .

The type of probability distribution depends on the type of test.

Common examples are:

• Standard Normal Distribution (Z): used for Testing Population Proportions
• Student's T-Distribution (T): used for Testing Population Means

Note: You will learn how to calculate the test statistic for each type of test in the following chapters.

The Critical Value and P-Value Approach

There are two main approaches used for hypothesis tests:

• The critical value approach compares the test statistic with the critical value of the significance level.
• The p-value approach compares the p-value of the test statistic and with the significance level.

The Critical Value Approach

The critical value approach checks if the test statistic is in the rejection region .

The rejection region is an area of probability in the tails of the distribution.

The size of the rejection region is decided by the significance level (\(\alpha\)).

The value that separates the rejection region from the rest is called the critical value .

Here is a graphical illustration:

If the test statistic is inside this rejection region, the null hypothesis is rejected .

For example, if the test statistic is 2.3 and the critical value is 2 for a significance level (\(\alpha = 0.05\)):

We reject the null hypothesis (\(H_{0} \)) at 0.05 significance level (\(\alpha\))

The P-Value Approach

The p-value approach checks if the p-value of the test statistic is smaller than the significance level (\(\alpha\)).

The p-value of the test statistic is the area of probability in the tails of the distribution from the value of the test statistic.

If the p-value is smaller than the significance level, the null hypothesis is rejected .

The p-value directly tells us the lowest significance level where we can reject the null hypothesis.

For example, if the p-value is 0.03:

We reject the null hypothesis (\(H_{0} \)) at a 0.05 significance level (\(\alpha\))

We keep the null hypothesis (\(H_{0}\)) at a 0.01 significance level (\(\alpha\))

Note: The two approaches are only different in how they present the conclusion.

Steps for a Hypothesis Test

The following steps are used for a hypothesis test:

• Check the conditions
• Define the claims
• Decide the significance level
• Calculate the test statistic

One condition is that the sample is randomly selected from the population.

The other conditions depends on what type of parameter you are testing the hypothesis for.

Common parameters to test hypotheses are:

• Proportions (for qualitative data)
• Mean values (for numerical data)

You will learn the steps for both types in the following pages.

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Confidence distributions and hypothesis testing

• Regular Article
• Open access
• Published: 29 March 2024

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• Eugenio Melilli   ORCID: orcid.org/0000-0003-2542-5286 1 &
• Piero Veronese   ORCID: orcid.org/0000-0002-4416-2269 1  

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The traditional frequentist approach to hypothesis testing has recently come under extensive debate, raising several critical concerns. Additionally, practical applications often blend the decision-theoretical framework pioneered by Neyman and Pearson with the inductive inferential process relied on the p -value, as advocated by Fisher. The combination of the two methods has led to interpreting the p -value as both an observed error rate and a measure of empirical evidence for the hypothesis. Unfortunately, both interpretations pose difficulties. In this context, we propose that resorting to confidence distributions can offer a valuable solution to address many of these critical issues. Rather than suggesting an automatic procedure, we present a natural approach to tackle the problem within a broader inferential context. Through the use of confidence distributions, we show the possibility of defining two statistical measures of evidence that align with different types of hypotheses under examination. These measures, unlike the p -value, exhibit coherence, simplicity of interpretation, and ease of computation, as exemplified by various illustrative examples spanning diverse fields. Furthermore, we provide theoretical results that establish connections between our proposal, other measures of evidence given in the literature, and standard testing concepts such as size, optimality, and the p -value.

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1 Introduction

In applied research, the standard frequentist approach to hypothesis testing is commonly regarded as a straightforward, coherent, and automatic method for assessing the validity of a conjecture represented by one of two hypotheses, denoted as \({{{\mathcal {H}}}_{0}}\) and \({{{\mathcal {H}}}_{1}}\) . The probabilities \(\alpha \) and \(\beta \) of committing type I and type II errors (reject \({{{\mathcal {H}}}_{0}}\) , when it is true and accept \({{{\mathcal {H}}}_{0}}\) when it is false, respectively) are controlled through a carefully designed experiment. After having fixed \(\alpha \) (usually at 0.05), the p -value is used to quantify the measure of evidence against the null hypothesis. If the p -value is less than \(\alpha \) , the conclusion is deemed significant , suggesting that it is unlikely that the null hypothesis holds. Regrettably, this methodology is not as secure as it may seem, as evidenced by a large literature, see the ASA’s Statement on p -values (Wasserstein and Lazar 2016 ) and The American Statistician (2019, vol. 73, sup1) for a discussion of various principles, misconceptions, and recommendations regarding the utilization of p -values. The standard frequentist approach is, in fact, a blend of two different views on hypothesis testing presented by Neyman-Pearson and Fisher. The first authors approach hypothesis testing within a decision-theoretic framework, viewing it as a behavioral theory. In contrast, Fisher’s perspective considers testing as a component of an inductive inferential process that does not necessarily require an alternative hypothesis or concepts from decision theory such as loss, risk or admissibility, see Hubbard and Bayarri ( 2003 ). As emphasized by Goodman ( 1993 ) “the combination of the two methods has led to a reinterpretation of the p -value simultaneously as an ‘observed error rate’ and as a ‘measure of evidence’. Both of these interpretations are problematic...”.

It is out of our scope to review the extensive debate on hypothesis testing. Here, we briefly touch upon a few general points, without delving into the Bayesian approach.

i) The long-standing caution expressed by Berger and Sellke ( 1987 ) and Berger and Delampady ( 1987 ) that a p -value of 0.05 provides only weak evidence against the null hypothesis has been further substantiated by recent investigations into experiment reproducibility, see e.g., Open Science Collaboration OSC ( 2015 ) and Johnson et al. ( 2017 ). In light of this, 72 statisticians have stated “For fields where the threshold for defining statistical significance for new discoveries is \(p<0.05\) , we propose a change to \(p<0.005\) ”, see Benjamin et al. ( 2018 ).

ii) The ongoing debate regarding the selection of a one-sided or two-sided test leaves the standard practice of doubling the p-value , when moving from the first to the second type of test, without consistent support, see e.g., Freedman ( 2008 ).

iii) There has been a longstanding argument in favor of integrating hypothesis testing with estimation, see e.g. Yates ( 1951 , pp. 32–33) or more recently, Greenland et al. ( 2016 ) who emphasize that “... statistical tests should never constitute the sole input to inferences or decisions about associations or effects ... in most scientific settings, the arbitrary classification of results into significant and non-significant is unnecessary for and often damaging to valid interpretation of data”.

iv) Finally, the p -value is incoherent when it is regarded as a statistical measure of the evidence provided by the data in support of a hypothesis \({{{\mathcal {H}}}_{0}}\) . As shown by Schervish ( 1996 ), it is possible that the p -value for testing the hypothesis \({{{\mathcal {H}}}_{0}}\) is greater than that for testing \({{{\mathcal {H}}}_{0}}^{\prime } \supset {{{\mathcal {H}}}_{0}}\) for the same observed data.

While theoretical insights into hypothesis testing are valuable for elucidating various aspects, we believe they cannot be compelled to serve as a unique, definitive practical guide for real-world applications. For example, uniformly most powerful (UMP) tests for discrete models not only rarely exist, but nobody uses them because they are randomized. On the other hand, how can a test of size 0.05 be considered really different from one of size 0.047 or 0.053? Moreover, for one-sided hypotheses, why should the first type error always be much more severe than the second type one? Alternatively, why should the test for \({{{\mathcal {H}}}_{0}}: \theta \le \theta _0\) versus \({{{\mathcal {H}}}_{1}}: \theta >\theta _0\) always be considered equivalent to the test for \({{{\mathcal {H}}}_{0}}: \theta = \theta _0\) versus \({{{\mathcal {H}}}_{1}}: \theta >\theta _0\) ? Furthermore, the decision to test \({{{\mathcal {H}}}_{0}}: \theta =\theta _0\) rather than \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _0-\epsilon , \theta _0+\epsilon ]\) , for a suitable positive \(\epsilon \) , should be driven by the specific requirements of the application and not solely by the existence of a good or simple test. In summary, we concur with Fisher ( 1973 ) that “no scientific worker has a fixed level of significance at which from year to year, and in all circumstances, he rejects hypotheses; he rather gives his mind to each particular case in the light of his evidence and his ideas”.

Considering all these crucial aspects, we believe it is essential to seek an applied hypothesis testing approach that encourages researchers to engage more deeply with the specific problem, avoids relying on standardized procedures, and is consistently integrated into a broader framework of inference. One potential solution can be found resorting to the “confidence distribution” (CD) approach. The modern CD theory was introduced by Schweder and Hjort ( 2002 ) and Singh et al. ( 2005 ) and relies on the idea of constructing a data-depending distribution for the parameter of interest to be used for inferential purposes. A CD should not be confused with a Bayesian posterior distribution. It is not derived through the Bayes theorem, and it does not require any prior distributions. Similar to the conventional practice in point or interval estimation, where one seeks a point or interval estimator, the objective of this theory is to discover a distribution estimator . Thanks to a clarification of this concept and a formalized definition of the CD within a purely frequentist setting, a wide literature on the topic has been developed encompassing both theoretical developments and practical applications, see e.g. for a general overview Schweder and Hjort ( 2016 ), Singh et al. ( 2007 ), and Xie and Singh ( 2013 ). We also remark that when inference is required for a real parameter, it is possible to establish a relationship between CDs and fiducial distributions, originally introduced by Fisher ( 1930 ). For a modern and general presentation of the fiducial inference see Hannig ( 2009 ) and Hannig et al. ( 2016 ), while for a connection with the CDs see Schweder and Hjort ( 2016 ) and Veronese and Melilli ( 2015 , 2018a ). Some results about the connection between CDs and hypothesis testing are presented in Singh et al. ( 2007 , Sec. 3.3) and Xie & Singh ( 2013 , Sec. 4.3), but the focus is only on the formal relationships between the support that a CD can provide for a hypothesis and the p -value.

In this paper we discuss in details the application of CDs in hypothesis testing. We show how CDs can offer valuable solutions to address the aforementioned difficulties and how a test can naturally be viewed as a part of a more extensive inferential process. Once a CD has been specified, everything can be developed straightforwardly, without any particular technical difficulties. The core of our approach centers on the notion of support provided by the data to a hypothesis through a CD. We introduce two distinct but related types of support, the choice of which depends on the hypothesis under consideration. They are always coherent, easy to interpret and to compute, even in case of interval hypotheses, contrary to what happens for the p -value. The flexibility, simplicity, and effectiveness of our proposal are illustrated by several examples from various fields and a simulation study. We have postponed the presentation of theoretical results, comparisons with other proposals found in the literature, as well as the connections with standard hypothesis testing concepts such as size, significance level, optimality, and p -values to the end of the paper to enhance its readability.

The paper is structured as follows: In Sect. 2 , we provide a review of the CD’s definition and the primary methods for its construction, with a particular focus on distinctive aspects that arise when dealing with discrete models (Sect. 2.1 ). Section 3 explores the application of the CD in hypothesis testing and introduces the two notions of support. In Sect. 4 , we discuss several examples to illustrate the benefits of utilizing the CD in various scenarios, offering comparisons with traditional p -values. Theoretical results about tests based on the CD and comparisons with other measures of support or plausibility for hypotheses are presented in Sect. 5 . Finally, in Sect. 6 , we summarize the paper’s findings and provide concluding remarks. For convenience, a table of CDs for some common statistical models can be found in Appendix A, while all the proofs of the propositions are presented in Appendix B.

2 Confidence distributions

The modern definition of confidence distribution for a real parameter \(\theta \) of interest, see Schweder & Hjort ( 2002 ; 2016 , sec. 3.2) and Singh et al. ( 2005 ; 2007 ) can be formulated as follows:

Definition 1

Let \(\{P_{\theta ,\varvec{\lambda }},\theta \in \Theta \subseteq \mathbb {R}, \varvec{\lambda }\in \varvec{\Lambda }\}\) be a parametric model for data \(\textbf{X}\in {\mathcal {X}}\) ; here \(\theta \) is the parameter of interest and \(\varvec{\lambda }\) is a nuisance parameter. A function H of \(\textbf{X}\) and \(\theta \) is called a confidence distribution for \(\theta \) if: i) for each value \(\textbf{x}\) of \(\textbf{X}\) , \(H(\textbf{x},\cdot )=H_{\textbf{x}}(\cdot )\) is a continuous distribution function on \(\Theta \) ; ii) \(H(\textbf{X},\theta )\) , seen as a function of the random element \(\textbf{X}\) , has the uniform distribution on (0, 1), whatever the true parameter value \((\theta , \varvec{\lambda })\) . The function H is an asymptotic confidence distribution if the continuity requirement in i) is removed and ii) is replaced by: ii) \(^{\prime }\) \(H(\textbf{X},\theta )\) converges in law to the uniform distribution on (0, 1) for the sample size going to infinity, whatever the true parameter value \((\theta , \varvec{\lambda })\) .

The CD theory is placed in a purely frequentist context and the uniformity of the distribution ensures the correct coverage of the confidence intervals. The CD should be regarded as a distribution estimator of a parameter \(\theta \) and its mean, median or mode can serve as point estimates of \(\theta \) , see Xie and Singh ( 2013 ) for a detailed discussion. In essence, the CD can be employed in a manner similar to a Bayesian posterior distribution, but its interpretation differs and does not necessitate any prior distribution. Closely related to the CD is the confidence curve (CC) which, given an observation \(\textbf{x}\) , is defined as \( CC_{\textbf{x}}(\theta )=|1-2H_{\textbf{x}}(\theta )|\) ; see Schweder and Hjort ( 2002 ). This function provides the boundary points of equal-tailed confidence intervals for any level \(1-\alpha \) , with \(0<\alpha <1\) , and offers an immediate visualization of their length.

Various procedures can be adopted to obtain exact or asymptotic CDs starting, for example, from pivotal functions, likelihood functions and bootstrap distributions, as detailed in Singh et al. ( 2007 ), Xie and Singh ( 2013 ), Schweder and Hjort ( 2016 ). A CD (or an asymptotic CD) can also be derived directly from a real statistic T , provided that its exact or asymptotic distribution function \(F_{\theta }(t)\) is a continuously monotonic function in \(\theta \) and its limits are 0 and 1 as \(\theta \) approaches its boundaries. For example, if \(F_{\theta }(t)\) is nonincreasing, we can define

Furthermore, if \(H_t(\theta )\) is differentiable in \(\theta \) , we can obtain the CD-density \(h_t(\theta )=-({\partial }/{\partial \theta }) F_{\theta }(t)\) , which coincides with the fiducial density suggested by Fisher. In particular, when the statistical model belongs to the real regular natural exponential family (NEF) with natural parameter \(\theta \) and sufficient statistic T , there always exists an “optimal” CD for \(\theta \) which is given by ( 1 ), see Veronese and Melilli ( 2015 ).

The CDs based on a real statistic play an important role in hypothesis testing. In this setting remarkable results are obtained when the model has monotone likelihood ratio (MLR). We recall that if \(\textbf{X}\) is a random vector distributed according to the family \(\{p_\theta , \theta \in \Theta \subseteq \mathbb {R}\}\) , this family is said to have MLR in the real statistic \(T(\textbf{X})\) if, for any \(\theta _1 <\theta _2\) , the ratio \(p_{\theta _2}(\textbf{x})/p_{\theta _1}(\textbf{x})\) is a nondecreasing function of \(T(\textbf{x})\) for values of \(\textbf{x}\) that induce at least one of \(p_{\theta _1}\) and \(p_{\theta _2}\) to be positive. Furthermore, for such families, it holds that \(F_{\theta _2}(t) \le F_{\theta _1}(t)\) for each t , see Shao ( 2003 , Sec. 6.1.2). Families with MLR not only allow the construction of Uniformly Most Powerful (UMP) tests in various scenarios but also identify the statistic T , which can be employed in constructing the CD for \(\theta \) . Indeed, because \(F_\theta (t)\) is nonincreasing in \(\theta \) for each t , \(H_t(\theta )\) can be defined as in ( 1 ) provided the conditions of continuity and limits of \(F_{\theta }(t)\) are met. Of course, if the MLR is nonincreasing in T a similar result holds and the CD for \(\theta \) is \(H_t(\theta )=F_\theta (t)\) .

An interesting characteristic of the CD that validates its suitability for use in a testing problem is its consistency , meaning that it increasingly concentrates around the “true” value of \(\theta \) as the sample size grows, leading to the correct decision.

Definition 2

The sequence of CDs \(H(\textbf{X}_n, \cdot )\) is consistent at some \(\theta _0 \in \Theta \) if, for every neighborhood U of \(\theta _0\) , \(\int _U dH(\textbf{X}_n, \theta ) \rightarrow 1\) , as \(n\rightarrow \infty \) , in probability under \(\theta _0\) .

The following proposition provides some useful asymptotic properties of a CD for independent identically distributed (i.i.d.) random variables.

Proposition 1

Let \(X_1,X_2,\ldots \) be a sequence of i.i.d. random variables from a distribution function \(F_{\theta }\) , parameterized by a real parameter \(\theta \) , and let \(H_{\textbf{x}_n}\) be the CD for \(\theta \) based on \(\textbf{x}_n=(x_1, \ldots , x_n)\) . If \(\theta _0\) denotes the true value of \(\theta \) , then \(H(\textbf{X}_n, \cdot )\) is consistent at \(\theta _0\) if one of the following conditions holds:

\(F_{\theta }\) belongs to a NEF;

\(F_{\theta }\) is a continuous distribution function and standard regularity assumptions hold;

its expected value and variance converge for \(n\rightarrow \infty \) to \(\theta _0\) , and 0, respectively, in probability under \(\theta _0\) .

Finally, if i) or ii) holds the CD is asymptotically normal.

Table 8 in Appendix A provides a list of CDs for various standard models. Here, we present two basic examples, while numerous others will be covered in Sect. 4 within an inferential and testing framework.

( Normal model ) Let \(\textbf{X}=(X_1,\ldots ,X_n)\) be an i.i.d. sample from a normal distribution N \((\mu ,\sigma ^2)\) , with \(\sigma ^2\) known. A standard pivotal function is \(Q({\bar{X}}, \mu )=\sqrt{n}({\bar{X}}-\mu )/ \sigma \) , where \(\bar{X}=\sum X_i/n\) . Since \(Q({\bar{X}}, \mu )\) is decreasing in \(\mu \) and has the standard normal distribution \(\Phi \) , the CD for \(\mu \) is \(H_{\bar{x}}(\mu )=1-\Phi (\sqrt{n}({\bar{x}}-\mu )/ \sigma )=\Phi (\sqrt{n}(\mu -{\bar{x}})/ \sigma )\) , that is a N \(({\bar{x}},\sigma /\sqrt{n})\) . When the variance is unknown we can use the pivotal function \(Q({\bar{X}}, \mu )=\sqrt{n}({\bar{X}}-\mu )/S\) , where \(S^2=\sum (X_i-\bar{X})^2/(n-1)\) , and the CD for \(\mu \) is \(H_{{\bar{x}},s}(\mu )=1-F^{T_{n-1}}(\sqrt{n}({\bar{x}}-\mu )/ \sigma )=F^{T_{n-1}}(\sqrt{n}(\mu -{\bar{x}})/ \sigma )\) , where \(F^{T_{n-1}}\) is the t-distribution function with \(n-1\) degrees of freedom.

( Uniform model ) Let \(\textbf{X}=(X_1,\ldots ,X_n)\) be an i.i.d. sample from the uniform distribution on \((0,\theta )\) , \(\theta >0\) . Consider the (sufficient) statistic \(T=\max (X_1, \ldots ,X_n)\) whose distribution function is \(F_\theta (t)=(t/\theta )^n\) , for \(0<t<\theta \) . Because \(F_\theta (t)\) is decreasing in \(\theta \) and the limit conditions are satisfied for \(\theta >t\) , the CD for \(\theta \) is \(H_t(\theta )=1-(t/\theta )^n\) , i.e. a Pareto distribution \(\text {Pa}(n, t)\) with parameters n (shape) and t (scale). Since the uniform distribution is not regular, the consistency of the CD follows from condition iii) of Proposition 1 . This is because \(E^{H_{t}}(\theta )=nt/(n-1)\) and \(Var^{H_{t}}(\theta )=nt^2/((n-2)(n-1)^2)\) , so that, for \(n\rightarrow \infty \) , \(E^{H_{t}}(\theta ) \rightarrow \theta _0\) (from the strong consistency of the estimator T of \(\theta \) , see e.g. Shao 2003 , p.134) and \(Var^{H_{t}}(\theta )\rightarrow 0\) trivially.

2.1 Peculiarities of confidence distributions for discrete models

When the model is discrete, clearly we can only derive asymptotic CDs. However, a crucial question arises regarding uniqueness. Since \(F_{\theta }(t)=\text{ Pr}_\theta \{T \le t\}\) does not coincide with Pr \(_\theta \{T<t\}\) for any value t within the support \({\mathcal {T}}\) of T , it is possible to define two distinct “extreme” CDs. If \(F_\theta (t)\) is non increasing in \(\theta \) , we refer to the right CD as \(H_{t}^r(\theta )=1-\text{ Pr}_\theta \{T\le t\}\) and to the left CD as \(H_{t}^\ell (\theta )=1-\text{ Pr}_\theta \{T<t\}\) . Note that \(H_{t}^r(\theta ) < H_{t}^\ell (\theta )\) , for every \(t \in {{\mathcal {T}}}\) and \(\theta \in \Theta \) , so that the center (i.e. the mean or the median) of \(H_{t}^r(\theta )\) is greater than that of \(H_{t}^\ell (\theta )\) . If \(F_\theta (t)\) is increasing in \(\theta \) , we define \( H_{t}^\ell (\theta )=F_\theta (t)\) and \(H^r_t(\theta )=\text{ Pr}_\theta \{T<t\}\) and one again \(H_{t}^r(\theta ) < H_{t}^\ell (\theta )\) . Veronese & Melilli ( 2018b , sec. 3.2) suggest overcoming this nonuniqueness by averaging the CD-densities \(h_t^r\) and \(h_t^\ell \) using the geometric mean \(h_t^g(\theta )\propto \sqrt{h_t^r(\theta )h_t^\ell (\theta )}\) . This typically results in a simpler CD compared to the one obtained through the arithmetic mean, with smaller confidence intervals. Note that the (asymptotic) CD defined in ( 1 ) for discrete models corresponds to the right CD, and it is more appropriately referred to as \(H_t^r(\theta )\) hereafter. Clearly, \(H_{t}^\ell (\theta )\) can be obtained from \(H_{t}^r(\theta )\) by replacing t with its preceding value in the support \({\mathcal {T}}\) . For discrete models, the table in Appendix A reports \(H_{t}^r(\theta )\) , \(H_{t}^\ell (\theta )\) and \(H_t^g(\theta )\) . Compared to \(H^{\ell }_t\) and \(H^r_t\) , \(H^g_t\) offers the advantage of closely approximating a uniform distribution when viewed as a function of the random variable T .

Proposition 2

Given a discrete statistic T with distribution indexed by a real parameter \(\theta \in \Theta \) and support \({{\mathcal {T}}}\) independent of \(\theta \) , assume that, for each \(\theta \in \Theta \) and \(t\in {\mathcal {T}}\) , \(H^r_t(\theta )< H^g_t(\theta ) < H^{\ell }_t(\theta )\) . Then, denoting by \(G^j\) the distribution function of \(H^j_T\) , with \(j=\ell ,g,r\) , we have \(G^\ell (u) \le u \le G^r(u)\) . Furthermore,

Notice that the assumption in Proposition 2 is always satisfied when the model belongs to a NEF, see Veronese and Melilli ( 2018a ).

The possibility of constructing different CDs using the same discrete statistic T plays an important role in connection with standard p -values, as we will see in Sect. 5 .

(Binomial model) Let \(\textbf{X}=(X_1,\ldots , X_n)\) be an i.i.d. sample from a binomial distributions Bi(1,  p ) with success probability p . Then \(T=\sum _{i=1}^n X_i\) is distributed as a Bi( n ,  p ) and by ( 1 ), recalling the well-known relationship between the binomial and beta distributions, it follows that the right CD for p is a Be( \(t+1,n-t\) ) for \(t=0,1,\ldots , n-1\) . Furthermore, the left CD is a Be( \(t,n-t+1\) ) and it easily follows that \(H_t^g(p)\) is a Be( \(t+1/2,n-t+1/2\) ). Figure 1 shows the corresponding three CD-densities along with their respective CCs, emphasizing the central position of \(h_t^g(p)\) and its confidence intervals in comparison to \(h_t^\ell (p)\) and \(h^r_t(p)\) .

(Binomial model) CD-densities (left plot) and CCs (right plot) corresponding to \(H_t^g(p)\) (solid lines), \(H_t^{\ell }(p)\) (dashed lines) and \(H_t^r(p)\) (dotted lines) for the parameter p with n = 15 and \(t=5\) . In the CC plot, the horizontal dotted line is at level 0.95

3 Confidence distributions in testing problems

As mentioned in Sect. 1 , we believe that introducing a CD can serve as a valuable and unifying approach, compelling individuals to think more deeply about the specific problem they aim to address rather than resorting to automatic rules. In fact, the availability of a whole distribution for the parameter of interest equips statisticians and practitioners with a versatile tool for handling a wide range of inference tasks, such as point and interval estimation, hypothesis testing, and more, without the need for ad hoc procedures. Here, we will address the issue in the simplest manner, referring to Sect. 5 for connections with related ideas in the literature and additional technical details.

Given a set \(A \subseteq \Theta \subseteq \mathbb {R}\) , it seems natural to measure the “support” that the data \(\textbf{x}\) provide to A through the CD \(H_{\textbf{x}}\) , as \(CD(A)=H_{\textbf{x}}(A)= \int _{A} dH_{\textbf{x}}(\theta )\) . Notice that, with a slight abuse of notation widely used in literature (see e.g., Singh et al. 2007 , who call \(H_{\textbf{x}}(A)\) strong-support ), we use \(H_{\textbf{x}}(\theta )\) to indicate the distribution function on \(\Theta \subseteq \mathbb {R}\) evaluated at \(\theta \) and \(H_{\textbf{x}}(A)\) to denote the mass that \(H_{\textbf{x}}\) induces on a (measurable) subset \(A\subseteq \Theta \) . It immediately follows that to compare the plausibility of k different hypotheses \({{\mathcal {H}}}_{i}: \theta \in \Theta _i\) , \(i=1,\ldots ,k\) , with \(\Theta _i \subseteq \Theta \) not being a singleton, it is enough to compute each \(H_{\textbf{x}}(\Theta _i)\) . We will call \(H_{\textbf{x}}(\Theta _i)\) the CD-support provided by \(H_{\textbf{x}}\) to the set \(\Theta _i\) . In particular, consider the usual case in which we have two hypotheses \({{{\mathcal {H}}}_{0}}: \theta \in \Theta _0\) and \({{{\mathcal {H}}}_{1}}: \theta \in \Theta _1\) , with \(\Theta _0 \cap \Theta _1= \emptyset \) , \(\Theta _0 \cup \Theta _1 = \Theta \) and assume that \({{{\mathcal {H}}}_{0}}\) is not a precise hypothesis (i.e. is not of type \(\theta =\theta _0\) ). As in the Bayesian approach one can compute the posterior odds, here we can evaluate the confidence odds \(CO_{0,1}\) of \({{{\mathcal {H}}}_{0}}\) against \({{{\mathcal {H}}}_{1}}\)

If \(CO_{0,1}\) is greater than one, the data support \({{{\mathcal {H}}}_{0}}\) more than \({{{\mathcal {H}}}_{1}}\) and this support clearly increases with \(CO_{0,1}\) . Sometimes this type of information can be sufficient to have an idea of the reasonableness of the hypotheses, but if we need to take a decision, we can include the confidence odds in a full decision setting. Thus, writing the decision space as \({{\mathcal {D}}}=\{0,1\}\) , where i indicates accepting \({{{\mathcal {H}}}}_i\) , for \(i=0,1\) , a penalization for the two possible errors must be specified. A simple loss function is

where \(\delta \) denotes the decision taken and \(a_i >0\) , \(i=0,1\) . The optimal decision is the one that minimizes the (expected) confidence loss

Therefore, we will choose \({{{\mathcal {H}}}_{0}}\) if \(a_0 H_{\textbf{x}}(\Theta _0) > a_1 H_{\textbf{x}}(\Theta _1)\) , that is if \(CO_{0,1}>a_1/a_0\) or equivalently if \(H_{\textbf{x}}(\Theta _0)>a_1/(a_0+a_1)=\gamma \) . Clearly, if there is no reason to penalize differently the two errors by setting an appropriate value for the ratio \(a_1/a_0\) , we assume \(a_0=a_1\) so that \(\gamma =0.5\) . This implies that the chosen hypothesis will be the one receiving the highest level of the CD-support. Therefore, we state the following

Definition 3

Given the two (non precise) hypotheses \({{\mathcal {H}}}_i: \theta \in \Theta _i\) , \(i=0,1\) , the CD-support of \({{\mathcal {H}}}_i\) is defined as \(H_{\textbf{x}}(\Theta _i)\) . The hypothesis \({{{\mathcal {H}}}_{0}}\) is rejected according to the CD-test if the CD-support is less than a fixed threshold \(\gamma \) depending on the loss function ( 3 ) or, equivalently, if the confidence odds \(CO_{0,1}\) are less than \(a_1/a_0=\gamma /(1-\gamma )\) .

Unfortunately, the previous notion of CD-support fails for a precise hypothesis \({{{\mathcal {H}}}_{0}}:\theta =\theta _0\) , since in this case \(H_{\textbf{x}}(\{\theta _0\})\) trivially equals zero. Notice that the problem cannot be solved by transforming \({{{\mathcal {H}}}_{0}}:\theta =\theta _0\) into the seemingly more reasonable \({{{\mathcal {H}}}_{0}}^{\prime }:\theta \in [\theta _0-\epsilon , \theta _0+\epsilon ]\) because, apart from the arbitrariness of \(\epsilon \) , the CD-support for very narrow range intervals would typically remain negligible. We thus introduce an alternative way to assess the plausibility of a precise hypothesis or, more generally, of a “small” interval hypothesis.

Consider first \({{{\mathcal {H}}}_{0}}:\theta =\theta _0\) and assume, as usual, that \(H_{\textbf{x}}(\theta )\) is a CD for \(\theta \) , based on the data \(\textbf{x}\) . Looking at the confidence curve \(CC_{\textbf{x}}(\theta )=|1-2H_{\textbf{x}}(\theta )|\) in Fig. 2 , it is reasonable to assume that the closer \(\theta _0\) is to the median \(\theta _m\) of the CD, the greater the consistency of the value of \(\theta _0\) with respect to \(\textbf{x}\) . Conversely, the complement to 1 of the CC represents the unconsidered confidence relating to both tails of the distribution. We can thus define a measure of plausibility for \({{{\mathcal {H}}}_{0}}:\theta =\theta _0\) as \((1-CC_{\textbf{x}}(\theta ))/2\) and this measure will be referred to as the CD*-support given by \(\textbf{x}\) to the hypothesis. It is immediate to see that

In other words, if \(\theta _0 < \theta _m\) \([\theta _0 > \theta _m]\) the CD*-support is \(H_{\textbf{x}}(\theta _0)\) \([1-H_{\textbf{x}}(\theta _0)]\) and corresponds to the CD-support of all \(\theta \) ’s that are less plausible than \(\theta _0\) among those located on the left [right] side of the CC . Clearly, if \(\theta _0 = \theta _m\) the CD*-support equals 1/2, its maximum value. Notice that in this case no alternative hypothesis is considered and that the CD*-support provides a measure of plausibility for \(\theta _0\) by examining “the direction of the observed departure from the null hypothesis”. This quotation is derived from Gibbons and Pratt ( 1975 ) and was originally stated to support their preference for reporting a one-tailed p -value over a two-tailed one. Here we are in a similar context and we refer to their paper for a detailed discussion of this recommendation.

The CD*-supports of the points \(\theta _0\) , \(\theta _1\) , \(\theta _m\) and \(\theta _2\) correspond to half of the solid vertical lines and are given by \(H_{\textbf{x}}(\theta _0)\) , \(H_{\textbf{x}}(\theta _1)\) , \(H_{\textbf{x}}(\theta _m)=1/2\) e \(1-H_{\textbf{x}}(\theta _2)\) , respectively

An alternative way to intuitively justify formula ( 4 ) is as follows. Since \(H_{\textbf{x}}(\{\theta _0\})=0\) , we can look at the set K of values of \(\theta \) which are in some sense “more consistent” with the observed data \(\textbf{x}\) than \(\theta _0\) , and define the plausibility of \({{{\mathcal {H}}}_{0}}\) as \(1-H_{\textbf{x}}(K)\) . This procedure was followed in a Bayesian framework by Pereira et al. ( 1999 ) and Pereira et al. ( 2008 ) who, in order to identify K , relay on the posterior distribution of \(\theta \) and focus on its mode. We refer to these papers for a more detailed discussion of this idea. Here we emphasize only that the evidence \(1-H_{\textbf{x}}(K)\) supporting \({{{\mathcal {H}}}_{0}}\) cannot be considered as evidence against a possible alternative hypothesis. In our context, the set K can be identified as the set \(\{\theta \in \Theta : \theta < \theta _0\}\) if \(H_{\textbf{x}}(\theta _0)>1-H_{\textbf{x}}(\theta _0)\) or as \(\{\theta \in \Theta : \theta >\theta _0\}\) if \(H_{\textbf{x}}(\theta _0)\le 1-H_{\textbf{x}}(\theta _0)\) . It follows immediately that \(1-H_{\textbf{x}}(K)=\min \{H_{\textbf{x}}(\theta _0), 1-H_{\textbf{x}}(\theta _0)\}\) , which coincides with the CD*-support given in ( 4 ).

We can readily extend the previous definition of CD*-support to interval hypotheses \({{{\mathcal {H}}}_{0}}:\theta \in [\theta _1, \theta _2]\) . This extension becomes particularly pertinent when dealing with small intervals, where the CD-support may prove ineffective. In such cases, the set K of \(\theta \) values that are “more consistent” with the data \(\textbf{x}\) than those falling within the interval \([\theta _1, \theta _2]\) should clearly exclude this interval. Instead, it should include one of the two tails, namely, either \({\theta \in \Theta : \theta < \theta _1}\) or \({\theta \in \Theta : \theta > \theta _2}\) , depending on which one receives a greater mass from the CD. Then

so that the CD*-support of the interval \([\theta _1,\theta _2]\) is \(\text{ CD* }([\theta _1,\theta _2])=1-H_{\textbf{x}}(K)=\min \{H_{\textbf{x}}(\theta _2), 1-H_{\textbf{x}}(\theta _1)\}\) , which reduces to ( 4 ) in the case of a degenerate interval (i.e., when \(\theta _1=\theta _2=\theta _0\) ). Therefore, we can establish the following

Definition 4

Given the hypothesis \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) , with \(\theta _1 \le \theta _2 \) , the CD*-support of \({{{\mathcal {H}}}_{0}}\) is defined as \(\min \{H_{\textbf{x}}(\theta _2), 1-H_{\textbf{x}}(\theta _1)\}\) . If \(H_{\textbf{x}}(\theta _2) <1-H_{\textbf{x}}(\theta _1)\) it is more reasonable to consider values of \(\theta \) greater than those specified by \({{{\mathcal {H}}}_{0}}\) , and conversely, the opposite holds true in the reverse situation. Furthermore, the hypothesis \({{{\mathcal {H}}}_{0}}\) is rejected according to the CD*-test if its CD*-support is less than a fixed threshold \(\gamma ^*\) .

The definition of CD*-support has been established for bounded interval (or precise) hypothesis. However, it can be readily extended to one-sided intervals such as \((-\infty , \theta _0]\) or \([\theta _0, +\infty )\) , but in these cases, it is evident that the CD*- and the CD-support are equivalent. For a general interval hypothesis we observe that \(H_{\textbf{x}}([\theta _1, \theta _2])\le \min \{H_{\textbf{x}}(\theta _2), 1-H_{\textbf{x}}(\theta _1)\}\) . Consequently, the CD-support can never exceed the CD*-support, even though they exhibit significant similarity when \(\theta _1\) or \(\theta _2\) resides in the extreme region of one tail of the CD or when the CD is highly concentrated (see examples 4 , 6 and 7 ).

It is crucial to emphasize that both CD-support and CD*-support are coherent measures of the evidence provided by the data for a hypothesis. This coherence arises from the fact that if \({{{\mathcal {H}}}_{0}}\subset {{{\mathcal {H}}}_{0}}^{\prime }\) , both the supports for \({{{\mathcal {H}}}_{0}}^{\prime }\) cannot be less than those for \({{{\mathcal {H}}}_{0}}\) . This is in stark contrast to the behavior of p -values, as demonstrated in Schervish ( 1996 ), Peskun ( 2020 ), and illustrated in Examples 4 and 7 .

Finally, as seen in Sect. 2.1 , various options for CDs are available for discrete models. Unless a specific problem suggests otherwise (see Sect. 5.1 ), we recommend using the geometric mean \(H_t^g\) as it offers a more impartial treatment of \({{{\mathcal {H}}}_{0}}\) and e \({{{\mathcal {H}}}_{1}}\) , as shown in Proposition 2 .

In this section, we illustrate the behavior, effectiveness, and simplicity of CD- and CD*-supports in an inferential context through several examples. We examine various contexts to assess the flexibility and consistency of our approach and compare it with the standard one. It is worth noting that the computation of the p -value for interval hypotheses is challenging and does not have a closed form.

( Normal model ) As seen in Example 1 , the CD for the mean \(\mu \) of a normal model is N \(({\bar{x}},\sigma /\sqrt{n})\) , for \(\sigma \) known. For simplicity, we assume this case; otherwise, the CD would be a t-distribution. Figure 3 shows the CD-density and the corresponding CC for \({\bar{x}}=2.7\) with three different values of \(\sigma /\sqrt{n}\) : \(1/\sqrt{50}=0.141\) , \(1/\sqrt{25}=0.2\) and \(1/\sqrt{10}=0.316\) .

The observed \({\bar{x}}\) specifies the center of both the CD and the CC, and values of \(\mu \) that are far from it receive less support the smaller the dispersion \(\sigma /\sqrt{n}\) of the CD. Alternatively, values of \(\mu \) within the CC, i.e., within the confidence interval of a specific level, are more reasonable than values outside it. These values become more plausible as the level of the interval decreases. Table 1 clarifies these points by providing the CD-support, confidence odds, CD*-support, and the p -value of the UMPU test for different interval hypotheses and different values of \(\sigma /\sqrt{n}\) .

(Normal model) CD-densities (left plot) and CCs (right plot) for \(\mu \) with \({\bar{x}}=2.7\) and three values of \(\sigma /\sqrt{n}\) : \(1/\sqrt{50}\) (solid line), \(1/\sqrt{25}\) (dashed line) and \(1/\sqrt{10}\) (dotted line). In the CC plot the dotted horizontal line is at level 0.95

It can be observed that when the interval is sufficiently large, e.g., [2.0, 2.5], the CD- and the CD*-supports are similar. However, for smaller intervals, as in the other three cases, the difference between the CD- and the CD*-support increases with the variance of the CD, \(\sigma /\sqrt{n}\) , regardless of whether the interval contains the observation \({\bar{x}}\) or not. These aspects are general depending on the form of the CD. Therefore, a comparison between these two measures can be useful to clarify whether an interval is smaller or not, according to the problem under analysis. Regarding the p -value of the UMPU test (see Schervish 1996 , equation 2), it is similar to the CD*-support when the interval is large (first case). However, the difference increases with the growth of the variance in the other cases. Furthermore, enlarging the interval from [2.4, 2.6] to [2.3, 2.6], not reported in Table 1 , while the CD*-supports remain unchanged, results in p -values reducing to 0.241, 0.331, and 0.479 for the three considered variances. This once again highlights the incoherence of the p -value as a measure of the plausibility of a hypothesis.

Now, consider a precise hypothesis, for instance, \({{{\mathcal {H}}}_{0}}:\mu =2.35\) . For the three values used for \(\sigma /\sqrt{n}\) , the CD*-supports are 0.007, 0.040, and 0.134, respectively. From Fig. 3 , it is evident that the point \(\mu =2.35\) lies to the left of the median of the CD. Consequently, the data suggest values of \(\mu \) larger than 2.35. Furthermore, looking at the CC, it becomes apparent that 2.35 is not encompassed within the confidence interval of level 0.95 when \(\sigma /\sqrt{n}=1/\sqrt{50}\) , contrary to what occurs in the other two cases. Due to the symmetry of the normal model, the UMPU test coincides with the equal tailed test, so that the p -value is equal to 2 times the CD*-support (see Remark 4 in Sect. 5.2 ). Furthermore, the size of the CD*-test is \(2\gamma ^*\) , where \(\gamma ^*\) is the threshold fixed to decide whether to reject the hypothesis or not (see Proposition 5 . Thus, if a test of level 0.05 is desired, it is sufficient to fix \(\gamma ^*=0.025\) , and both the CD*-support and the p -value lead to the same decision, namely, rejecting \({{{\mathcal {H}}}_{0}}\) only for the case \(\sigma /\sqrt{n}=0.141\) .

To assess the effectiveness of the CD*-support, we conduct a brief simulation study. For different values of \(\mu \) , we generate 100000 values of \({\bar{x}}\) from a normal distribution with mean \(\mu \) and various standard deviation \(\sigma /\sqrt{n}\) . We obtain the corresponding CDs with the CD*-supports and compute also the p -values. In Table 2 , we consider \({{{\mathcal {H}}}_{0}}: \mu \in [2.0, 2.5]\) and the performance of the CD*-support can be evaluated looking for example at the proportions of values in the intervals [0, 0.4), [0.4, 0.6) and [0.6, 1]. Values of the CD*-support in the first interval suggest a low plausibility of \({{{\mathcal {H}}}_{0}}\) in the light of the data, while values in the third one suggest a high plausibility. We highlight the proportions of incorrect evaluations in boldface. The last column of the table reports the proportion of errors resulting from the use of the standard procedure based on the p -value for a threshold of 0.05. Note how the proportion of errors related to the CD*-support is generally quite low with a maximum value of 0.301, contrary to what happens for the automatic procedure based on the p -value, which reaches a proportion of error of 0.845. Notice that the maximum error due to the CD*-support is obtained when \({{{\mathcal {H}}}_{0}}\) is true, while that due to the p -value is obtained in the opposite, as expected.

We consider now the two hypotheses \({{{\mathcal {H}}}_{0}}:\mu =2.35\) and \({{{\mathcal {H}}}_{0}}: \mu \in [2.75,2.85]\) . Notice that the interval in the second hypothesis should be regarded as small, because it can be checked that the CD- and CD*-supports consistently differ, as can be seen for example in Table 1 for the case \({\bar{x}}=2.7\) . Thus, this hypothesis can be considered not too different from a precise one. Because for a precise hypothesis the CD*-support cannot be larger than 0.5, to evaluate the performance of the CD*-support we can consider the three intervals [0, 0.2), [0.2, 0.3) and [0.3, 0.5].

Table 3 reports the results of the simulation including again the proportion of errors resulting from the use of the p -value with threshold 0.05. For the precise hypothesis \({{{\mathcal {H}}}_{0}}: \mu =2.35\) , the proportion of values of the CD*-support less than 0.2 when \(\mu =2.35\) is, whatever the standard deviation, approximately equal to 0.4. This depends on the fact that for a precise hypothesis, the CD*-support has a uniform distribution on the interval [0, 0.5], see Proposition 5 . This aspect must be taken into careful consideration when setting a threshold for a CD*-test. On the other hand, the proportion of values of the CD*-support in the interval [0.3, 0.5], which wrongly support \({{{\mathcal {H}}}_{0}}\) when it is false, goes from 0.159 to 0.333 for \(\mu =2.55\) and from 0.010 to 0.193 for \(\mu =2.75\) , which are surely better than those obtained from the standard procedure based on the p -value. Take now the hypothesis \({{{\mathcal {H}}}_{0}}: \mu \in [2.75,2.85]\) . Since it can be considered not too different from a precise hypothesis, we consider the proportion of values of the CD*-support in the intervals [0, 0.2), [0.2, 0.3) and [0.3, 1]. Notice that, for simplicity, we assume 1 as the upper bound of the third interval, even though for small intervals, the values of the CD*-support can not be much larger than 0.5. In our simulation it does not exceed 0.635. For the different values of \(\mu \) considered the behavior of the CD*-support and p -value is not too different from the previous case of a precise hypothesis even if the proportion of errors when \({{{\mathcal {H}}}_{0}}\) is true decreases for both while it increases when \({{{\mathcal {H}}}_{0}}\) is false.

Binomial model Suppose we are interested in assessing the chances of candidate A winning the next ballot for a certain administrative position. The latest election poll based on a sample of size \(n=20\) , yielded \(t=9\) votes in favor of A . What can we infer? Clearly, we have a binomial model where the parameter p denotes the probability of having a vote in favor of A . The standard estimate of p is \(\hat{p}=9/20=0.45\) , which might suggest that A will lose the ballot. However, the usual (Wald) confidence interval of level 0.95 based on the normal approximation, i.e. \(\hat{p} \pm 1.96 \sqrt{\hat{p}(1-\hat{p})/n}\) , is (0.232, 0.668). Given its considerable width, this interval suggests that the previous estimate is unreliable. We could perform a statistical test with a significance level \(\alpha \) , but what is \({{{\mathcal {H}}}_{0}}\) , and what value of \(\alpha \) should we consider? If \({{{\mathcal {H}}}_{0}}: p \ge 0.5\) , implying \({{{\mathcal {H}}}_{1}}: p <0.5\) , the p -value is 0.327. This suggests not rejecting \({{{\mathcal {H}}}_{0}}\) for any usual value \(\alpha \) . However, if we choose \({{{\mathcal {H}}}_{0}}^\prime : p \le 0.5\) the p -value is 0.673, and in this case, we would not reject \({{{\mathcal {H}}}_{0}}^\prime \) . These results provide conflicting indications. As seen in Example 3 , the CD for p , \(H_t^g(p)\) , is Be(9.5,11.5) and Fig. 4 shows its CD-density along with the corresponding CC, represented by solid lines. The dotted horizontal line at 0.95 in the CC plot highlights the (non asymptotic) equal-tailed confidence interval (0.251, 0.662), which is shorter than the Wald interval. Note that our interval can be easily obtained by computing the quantiles of order 0.025 and 0.975 of the beta distribution.

(Binomial model) CD-densities (left plot) and CCs (right plot) corresponding to \(H_t^g(p)\) , for the parameter p , with \(\hat{p}=t/n=0.45\) : \(n=20\) , \(t=9\) (solid lines) and \(n=60\) , \(t=27\) (dashed lines). In the CC plot the horizontal dotted line is at level 0.95

The CD-support provided by the data for the two hypotheses \({{{\mathcal {H}}}_{0}}:p \ge 0.5\) and \({{{\mathcal {H}}}_{1}}:p < 0.5\) (the choice of what is called \(H_0\) being irrelevant), is \(1-H_t^g(0.5)=0.328\) and \(H_t^g(0.5)=0.672\) respectively. Therefore, the confidence odds are \(CO_{0,1}=0.328/0.672=0.488\) , suggesting that the empirical evidence in favor of the victory of A is half of that of its defeat. Now, consider a sample of size \(n=60\) with \(t=27\) , so that again \(\hat{p}=0.45\) . While a standard analysis leads to the same conclusions (the p -values for \({{{\mathcal {H}}}_{0}}\) and \({{{\mathcal {H}}}_{0}}^{\prime }\) are 0.219 and 0.781, respectively), the use of the CD clarifies the differences between the two cases. The corresponding CD-density and CC are also reported in Fig. 4 (dashed lines) and, as expected, they are more concentrated around \(\hat{p}\) . Thus, the accuracy of the estimates of p is greater for the larger n and the length of the confidence intervals is smaller. Furthermore, for \(n=60\) , \(CO_{0,1}=0.281\) reducing the chance that A wins to about 1 to 4.

As a second application on the binomial model, we follow Johnson and Rossell ( 2010 ) and consider a stylized phase II trial of a new drug designed to improve the overall response rate from 20% to 40% for a specific population of patients with a common disease. The hypotheses are \({{{\mathcal {H}}}_{0}}:p \le 0.2\) versus \({{{\mathcal {H}}}_{1}}: p>0.2\) . It is assumed that patients are accrued and the trial continues until one of the two events occurs: (a) data clearly support one of the two hypotheses (indicated by a CD-support greater than 0.9) or (b) 50 patients have entered the trial. Trials that are not stopped before the 51st patient accrues are assumed to be inconclusive.

Based on a simulation of 1000 trials, Table 4 reports the proportions of trials that conclude in favor of each hypothesis, along with the average number of patients observed before each trial is stopped, for \(\theta =0.1\) (the central value of \({{{\mathcal {H}}}_{0}}\) ) and for \(\theta =0.4\) . A comparison with the results reported by Johnson and Rossell ( 2010 ) reveals that our approach is clearly superior with respect to Bayesian inferences performed with standard priors and comparable to that obtained under their non-local prior carefully specified. Although there is a slight reduction in the proportion of trials stopped for \({{\mathcal {H}}}_0\) (0.814 compared to 0.91), the average number of involved patients is lower (12.7 compared to 17.7), and the power is higher (0.941 against 0.812).

(Exponential distribution) Suppose an investigator aims to compare the performance of a new item, measured in terms of average lifetime, with that of the one currently in use, which is 0.375. To model the item lifetime, it is common to use the exponential distribution with rate parameter \(\lambda \) , so that the mean is \(1/\lambda \) . The typical testing problem is defined by \({{\mathcal {H}}}_0: \lambda =1/0.375=2.667\) versus \({{\mathcal {H}}}_1: \lambda \ne 2.667\) . In many cases, it would be more realistic and interesting to consider hypotheses of the form \({{\mathcal {H}}}_0: \lambda \in [\lambda _1,\lambda _2]\) versus \({{\mathcal {H}}}_1: \lambda \notin [\lambda _1,\lambda _2]\) , and if \({{{\mathcal {H}}}_{0}}\) is rejected, it becomes valuable to know whether the new item is better or worse than the old one. Note that, although an UMPU test exists for this problem, calculating its p -value is not simple and cannot be expressed in a closed form. Here we consider two different null hypotheses: \({{\mathcal {H}}}_0: \lambda \in [2, 4]\) and \({{\mathcal {H}}}_0: \lambda \in [2.63, 2.70]\) , corresponding to a tolerance in the difference between the mean lifetimes of the new and old items equal to 0.125 and 0.005, respectively. Given a sample of n new items with mean \({\bar{x}}\) , it follows from Table 8 in Appendix A that the CD for \(\lambda \) is Ga( n ,  t ), where \(t=n\bar{x}\) . Assuming \(n=10\) , we consider two values of t , namely, 1.5 and 4.5. The corresponding CD-densities are illustrated in Fig. 5 showing how the observed value t significantly influences the shape of the distribution, altering both its center and its dispersion, in contrast to the normal model. Specifically, for \(t=1.5\) , the potential estimates of \(\lambda \) , represented by the mean and median of the CD, are 6.67 and 6.45, respectively. For \(t=4.5\) , these values change to 2.22 and 2.15.

Table 5 provides the CD- and the CD*-supports corresponding to the two null hypotheses considered, along with the p -values of the UMPU test. Figure 5 and Table 5 together make it evident that, for \(t=1.5\) , the supports of both interval null hypotheses are very low and leading to their rejection, unless the problem requires a loss function that strongly penalizes a wrong rejection. Furthermore, it is immediately apparent that the data suggest higher values of \(\lambda \) , indicating a lower average lifetime of the new item. Note that the standard criterion “ p -value \(< 0.05\) ” would imply not rejecting \({{{\mathcal {H}}}_{0}}: \lambda \in [2,4]\) . For \(t=4.5\) , when \({{{\mathcal {H}}}_{0}}: \lambda \in [2,4]\) , the median 2.15 of the CD falls within the interval [2, 4]. Consequently, both the CD- and the CD*-supports are greater than 0.5, leading to the acceptance of \({{{\mathcal {H}}}_{0}}\) , as also suggested by the p -value. When \({{{\mathcal {H}}}_{0}}: \lambda \in [2.63, 2.70]\) , the CD-support becomes meaningless, whereas the CD*-support is not negligible (0.256) and should be carefully evaluated in accordance with the problem under analysis. This contrasts with the indication provided by the p -value (0.555).

For the point null hypothesis \(\lambda =2.67\) , the analysis is similar to that for the interval [2.63, 2.70]. Note that, in this case, in addition to the UMPU test, it is also possible to consider the simpler and most frequently used equal-tailed test. The corresponding p -value is 0.016 for \(t=1.5\) and 0.484 for \(t=4.5\) ; these values are exactly two times the CD*-support, see Remark 4 .

(Exponential model) CD-densities for the rate parameter \(\lambda \) , with \(n=10\) and \(t=1.5\) (dashed line) and \(t=4.5\) (solid line)

( Uniform model ) As seen in Example 2 , the CD for the parameter \(\theta \) of the uniform distribution \(\text {U}(0, \theta )\) is a Pareto distribution \(\text {Pa}(n, t)\) , where t is the sample maximum. Figure 6 shows the CD-density for \(n=10\) and \(t=2.1\) .

Consider now \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1, \theta _2]\) versus \({{{\mathcal {H}}}_{1}}: \theta \notin [\theta _1, \theta _2]\) . As usual, we can identify the interval \([\theta _1, \theta _2]\) on the plot of the CD-density and immediately recognize when the CD-test trivially rejects \({{{\mathcal {H}}}_{0}}\) (the interval lies on the left of t , i.e. \(\theta _2<t\) ), when the value of \(\theta _1\) is irrelevant and only the CD-support of \([t,\theta _2]\) determines the decision ( \(\theta _1<t<\theta _2\) ), or when the whole CD-support of \([\theta _1,\theta _2]\) must be considered ( \(t<\theta _1<\theta _2\) ). These facts are not as intuitive when the p -value is used. Indeed, for this problem, there exists the UMP test of level \(\alpha \) (see Eftekharian and Taheri 2015 ) and it is possible to write the p -value as

(we are not aware of previous mention of it). Table 6 reports the p -value of the UMP test, as well as the CD and CD*-supports, for the two hypotheses \({{{\mathcal {H}}}_{0}}: \theta \in [1.5, 2.2]\) and \({{{\mathcal {H}}}_{0}}^\prime : \theta \in [2.0, 2.2]\) for a sample of size \(n=10\) and various values of t .

It can be observed that, when t belongs to the interval \([\theta _1, \theta _2]\) , the CD- and CD*-supports do not depend on \(\theta _1\) , as previously remarked, while the p -value does. This reinforces the incoherence of the p -value shown by Schervish ( 1996 ). For instance, when \(t=2.19\) , the p -value for \({{{\mathcal {H}}}_{0}}\) is 0.046, while that for \({{{\mathcal {H}}}_{0}}^{\prime }\) (included in \({{{\mathcal {H}}}_{0}}\) ) is larger, namely 0.072. Thus, assuming \(\alpha =0.05\) , the UMP test leads to the rejection of \({{{\mathcal {H}}}_{0}}\) but it results in the acceptance of the smaller hypothesis \({{{\mathcal {H}}}_{0}}^{\prime }\) .

(Uniform model) CD-density for \(\theta \) with \(n=10\) and \(t=2.1\)

( Sharpe ratio ) The Sharpe ratio is one of the most widely used measures of performance of stocks and funds. It is defined as the average excess return relative to the volatility, i.e. \(SR=\theta =(\mu _R-R_f)/\sigma _R\) , where \(\mu _R\) and \(\sigma _R\) are the mean and standard deviation of a return R and \(R_f\) is a risk-free rate. Under the typical assumption of constant risk-free rate, the excess returns \(X_1, X_2, \ldots , X_n\) of the fund over a period of length n are considered, leading to \(\theta =\mu /\sigma \) , where \(\mu \) and \(\sigma \) are the mean and standard deviation of each \(X_i\) . If the sample is not too small, the distribution and the dependence of the \(X_i\) ’s are not so crucial, and the inference on \(\theta \) is similar to that obtained under the basic assumption of i.i.d. normal random variables, as discussed in Opdyke ( 2007 ). Following this article, we consider the weekly returns of the mutual fund Fidelity Blue Chip Growth from 12/24/03 to 12/20/06 (these data are available for example on Yahoo! Finance, https://finance.yahoo.com/quote/FBGRX ) and assume that the excess returns are i.i.d. normal with a risk-free rate equal to 0.00052. Two different samples are analyzed: the first one includes all \(n_1=159\) observations from the entire period, while the second one is limited to the \(n_2=26\) weeks corresponding to the fourth quarter of 2005 and the first quarter of 2006. The sample mean, the standard deviation, and the corresponding sample Sharpe ratio for the first sample are \(\bar{x}_1=0.00011\) , \(s_1=0.01354\) , \(t_1=\bar{x}_1/s_1=0.00842\) . For the second sample, the values are \(\bar{x}_2=0.00280\) , \(s_2=0.01048\) , \(t_2=\bar{x}_2/s_2=0.26744\) .

We can derive the CD for \(\theta \) starting from the sampling distribution of the statistic \(W=\sqrt{n}T=\sqrt{n}\bar{X}/S\) , which has a noncentral t-distribution with \(n-1\) degrees of freedom and noncentrality parameter \(\tau =\sqrt{n}\mu /\sigma =\sqrt{n}\theta \) . This family has MLR (see Lehmann and Romano 2005 , p. 224) and the distribution function \(F^W_\tau \) of W is continuous in \(\tau \) with \(\lim _{\tau \rightarrow +\infty } F^W_\tau (w)=0\) and \(\lim _{\tau \rightarrow -\infty } F^W_\tau (w)=1\) , for each w in \(\mathbb {R}\) . Thus, from ( 1 ), the CD for \(\tau \) is \(H^\tau _w(\tau )=1-F^W_\tau (w)\) . Recalling that \(\theta =\tau /\sqrt{n}\) , the CD for \(\theta \) can be obtained using a trivial transformation which leads to \(H^\theta _w(\theta )=H^\tau _{w}(\sqrt{n}\theta )=1-F_{\sqrt{n}\theta }^W(w)\) , where \(w=\sqrt{n}t\) . In Figure 7 , the CD-densities for \(\theta \) relative to the two samples are plotted: they are symmetric and centered on the estimate t of \(\theta \) , and the dispersion is smaller for the one with the larger n .

Now, let us consider the typical hypotheses for the Sharpe ratio \({{\mathcal {H}}}_0: \theta \le 0\) versus \({{\mathcal {H}}}_1: \theta >0\) . From Table 7 , which reports the CD-supports and the corresponding odds for the two samples, and from Fig. 7 , it appears that the first sample clearly favors neither hypothesis, while \({{{\mathcal {H}}}_{1}}\) is strongly supported by the second one. Here, the p -value coincides with the CD-support (see Proposition 3 ), but choosing the the usual values 0.05 or 0.01 to decide whether to reject \({{{\mathcal {H}}}_{0}}\) or not may lead to markedly different conclusions.

When the assumption of i.i.d. normal returns does not hold, it is possible to show (Opdyke 2007 ) that the asymptotic distribution of T is normal with mean and variance \(\theta \) and \(\sigma ^2_T=(1+\theta ^2(\gamma _4-1)/4-\theta \gamma _3)/n\) , where \(\gamma _3\) and \(\gamma _4\) are the skewness and kurtosis of the \(X_i\) ’s. Thus, the CD for \(\theta \) can be derived from the asymptotic distribution of T and is N( \(t,\hat{\sigma }^2_T)\) , where \(\hat{\sigma }^2_T\) is obtained by estimating the population moments using the sample counterparts. The last column of Table 7 shows that the asymptotic CD-supports for \({{{\mathcal {H}}}_{0}}\) are not too different from the previous ones.

(Sharpe ratio) CD-densities for \(\theta =\mu /\sigma \) with \(n_1=159, t_1=0.008\) (solid line) and \(n_2\) =26, \(t_2=0.267\) (dashed line)

( Ratio of Poisson rates ) The comparison of Poisson rates \(\mu _1\) and \(\mu _2\) is important in various contexts, as illustrated for example by Lehmann & Romano ( 2005 , sec. 4.5), who also derive the UMPU test for the ratio \(\phi =\mu _1/\mu _2\) . Given two i.i.d. samples of sizes \(n_1\) and \(n_2\) from independent Poisson distributions, we can summarize the data with the two sufficient sample sums \(S_1\) and \(S_2\) , where \(S_i \sim \) Po( \(n_i\mu _i\) ), \(i=1,2\) . Reparameterizing the joint density of \((S_1, S_2)\) with \(\phi =\mu _1/\mu _2\) and \(\lambda =n_1\mu _1+n_2\mu _2\) , it is simple to verify that the conditional distribution of \(S_1\) given \(S_1+S_2=s_1+s_2\) is Bi( \(s_1+s_2, w\phi /(1+w\phi )\) ), with \(w=n_1/n_2\) , while the marginal distribution of \(S_1+S_2\) depends only on \(\lambda \) . Thus, for making inference on \(\phi \) , it is reasonable to use the CD for \(\phi \) obtained from the previous conditional distribution. Referring to the table in Appendix A, the CD \(H^g_{s_1,s_2}\) for \(w\phi /(1+w\phi )\) is Be \((s_1+1/2, s_2+1/2)\) , enabling us to determine the CD-density for \(\phi \) through the change of variable rule:

We compare our results with those derived by the standard conditional test implemented through the function poisson.test in R. We use the “eba1977” data set available in the package ISwR, ( https://CRAN.R-project.org/package=ISwR ), which contains counts of incident lung cancer cases and population size in four neighboring Danish cities by age group. Specifically, we compare the \(s_1=11\) lung cancer cases in a population of \(n_1=800\) people aged 55–59 living in Fredericia with the \(s_2=21\) cases observed in the other cities, which have a total of \(n_2=3011\) residents. For the hypothesis \({{{\mathcal {H}}}_{0}}: \phi =1\) versus \({{{\mathcal {H}}}_{1}}: \phi \ne 1\) , the R-output provides a p -value of 0.080 and a 0.95 confidence interval of (0.858, 4.277). If a significance level \(\alpha =0.05\) is chosen, \({{{\mathcal {H}}}_{0}}\) is not rejected, leading to the conclusion that there should be no reason for the inhabitants of Fredericia to worry.

Looking at the three CD-densities for \(\phi \) in Fig. 8 , it is evident that values of \(\phi \) greater than 1 are more supported than values less than 1. Thus, one should test the hypothesis \({{{\mathcal {H}}}_{0}}: \phi \le 1\) versus \({{{\mathcal {H}}}_{1}}: \phi >1\) . Using ( 5 ), it follows that the CD-support of \({{{\mathcal {H}}}_{0}}\) is \(H^g_{s_1,s_2}(1)=0.037\) , and the confidence odds are \(CO_{0,1}=0.037/(1-0.037)=0.038\) . To avoid rejecting \({{{\mathcal {H}}}_{0}}\) , a very asymmetric loss function should be deemed suitable. Finally, we observe that the confidence interval computed in R, is the Clopper-Pearson one, which has exact coverage but, as generally recognized, is too wide. In our context, this corresponds to taking the lower bound of the interval using the CC generated by \(H^\ell _{s_1, s_2}\) and the upper bound using that generated by \(H^r_{s_1, s_2}\) (see Veronese and Melilli 2015 ). It includes the interval generated by \(H_{s_1, s_2}^g\) , namely (0.931, 4.026), as shown in the right plot of Fig. 8 .

(Poisson-rates) CD-densities (left plot) and CCs (right plot) corresponding to \(H^g_{s_1,s_2}(\phi )\) (solid lines), \(H^\ell _{s_1,s_2}(\phi )\) (dashed lines) and \(H^r_{s_1,s_2}(\phi )\) (dotted lines) for the parameter \(\phi \) . In the CC plot the vertical lines identify the Clopper-Pearson confidence interval (dashed and dotted lines) and that based on \(H^g_{s_1,s_2}(\phi )\) (solid lines). The dotted horizontal line is at level 0.95

5 Properties of CD-support and CD*-support

5.1 one-sided hypotheses.

The CD-support of a set is the mass assigned to it by the CD, making it a fundamental component in all inferential problems based on CDs. Nevertheless, its direct utilization in hypothesis testing is rare, with the exception of Xie and Singh ( 2013 ). It can also be viewed as a specific instance of evidential support , a notion introduced by Bickel ( 2022 ) within a broader category of models known as evidential models , which encompass both posterior distributions and confidence distributions as specific cases.

Let us now consider a classical testing problem. Let \(\textbf{X}\) be an i.i.d. sample with a distribution depending on a real parameter \(\theta \) and let \({{{\mathcal {H}}}_{0}}: \theta \le \theta _0\) versus \({{{\mathcal {H}}}_{1}}: \theta >\theta _0\) , where \(\theta _0\) is a fixed value (the case \({{{\mathcal {H}}}_{0}}^\prime : \theta \ge \theta _0\) versus \({{{\mathcal {H}}}_{1}}^\prime : \theta <\theta _0\) is perfectly specular and will not be analyzed). In order to compare our test with the standard one, we assume that the model has MLR in \(T=T(\textbf{X})\) . Suppose first that the distribution function \(F_\theta (t)\) of T is continuous and that the CD for \(\theta \) is \(H_t(\theta )=1- F_{\theta }(t)\) . From Sect. 3 , the CD-support for \({{{\mathcal {H}}}_{0}}\) (which coincides with the CD*-support) is \(H_t(\theta _0)\) . In this case, the UMP test exists, as established by the Karlin-Rubin theorem, and rejects \({{{\mathcal {H}}}_{0}}\) if \(t > t_\alpha \) , where \(t_\alpha \) depends on the chosen significance level \(\alpha \) , or alternatively, if the p -value \(\text{ Pr}_{\theta _0}(T\ge t)\) is less than \(\alpha \) . Since \(\text{ Pr}_{\theta _0}(T\ge t)=1-F_{\theta _0}(t)=H_t(\theta _0)\) , the p -value coincides with the CD-support. Thus, to define a CD-test with size \(\alpha \) , it is enough to fix its rejection region as \(\{t: H_t(\theta _0)<\alpha \}\) , and both tests lead to the same conclusion.

When the statistic T is discrete, we have seen that various choices of CDs are possible. Assuming that \(H^r_t(\theta )< H^g_t(\theta ) < H^{\ell }_t(\theta )\) , as occurs for models belonging to a real NEF, it follows immediately that \(H^{r}_t\) provides stronger support for \({{\mathcal {H}}}_0: \theta \le \theta _0\) than \(H^g_t\) does, while \(H^{\ell }_t\) provides stronger support for \({{\mathcal {H}}}_0^\prime : \theta \ge \theta _0\) than \(H^g_t\) does. In other words, \(H_t^{\ell }\) is more conservative than \(H^g_t\) for testing \({{{\mathcal {H}}}_{0}}\) and the same happens to \(H^r_t\) for \({{{\mathcal {H}}}_{0}}^{\prime }\) . Therefore, selecting the appropriate CD can lead to the standard testing result. For example, in the case of \({{{\mathcal {H}}}_{0}}:\theta \le \theta _0\) versus \({{{\mathcal {H}}}_{1}}: \theta > \theta _0\) , the p -value is \(\text{ Pr}_{\theta _0}(T\ge t)=1-\text{ Pr}_{\theta _0}(T<t)=H^{\ell }_t(\theta _0)\) , and the rejection region of the standard test and that of the CD-test based on \(H_t^{\ell }\) coincide if the threshold is the same. However, as both tests are non-randomized, their size is typically strictly less than the fixed threshold.

The following proposition summarizes the previous considerations.

Proposition 3

Consider a model indexed by a real parameter \(\theta \) with MLR in the statistic T and the one-sided hypotheses \({{{\mathcal {H}}}_{0}}: \theta \le \theta _0\) versus \({{{\mathcal {H}}}_{1}}: \theta >\theta _0\) , or \({{{\mathcal {H}}}_{0}}^\prime : \theta \ge \theta _0\) versus \({{{\mathcal {H}}}_{1}}^\prime : \theta <\theta _0\) . If T is continuous, then the CD-support and the p -value associated with the UMP test are equal. Thus, if a common threshold \(\alpha \) is set for both rejection regions, the two tests have size \(\alpha \) . If T is discrete, the CD-support coincides with the usual p -value if \(H^\ell _t [H^r_t]\) is chosen when \({{{\mathcal {H}}}_{0}}: \theta \le \theta _0\) \([{{{\mathcal {H}}}_{0}}^\prime : \theta \ge \theta _0]\) . For a fixed threshold \(\alpha \) , the two tests have a size not greater than \(\alpha \) .

The CD-tests with threshold \(\alpha \) mentioned in the previous proposition have significance level \(\alpha \) and are, therefore, valid , that is \(\sup _{\theta \in \Theta _0} Pr_\theta (H(T)\le \alpha ) \le \alpha \) (see Martin and Liu 2013 ). This is no longer true if, for a discrete T , we choose \(H^g_t\) . However, Proposition 2 implies that its average size is closer to \(\alpha \) compared to those of the tests obtained using \(H^\ell _t\) \([H^r_t]\) , making \(H^g_t\) more appropriate when the problem does not strongly suggest that the null hypothesis should be considered true “until proven otherwise”.

5.2 Precise and interval hypotheses

The notion of CD*-support surely demands more attention than that of CD-support. Recalling that the CD*-support only accounts for one direction of deviation from the precise or interval hypothesis, we will first briefly explore its connections with similar notions.

While the CD-support is an additive measure, meaning that for any set \(A \subseteq \Theta \) and its complement \(A^c\) , we always have \(\text{ CD }(A) +\text{ CD }(A^c)=1\) , the CD*-support is only a sub-additive measure, that is \(\text{ CD* }(A) +\text{ CD* }(A^c)\le 1\) , as can be easily checked. This suggests that the CD*-support can be related to a belief function. In essence, a belief function \(\text{ bel}_\textbf{x}(A)\) measures the evidence in \(\textbf{x}\) that supports A . However, due to its sub-additivity, it alone cannot provide sufficient information; it must be coupled with the plausibility function, defined as \(\text {pl}_\textbf{x}(A) = 1 - \text {bel}_\textbf{x}(A^c)\) . We refer to Martin and Liu ( 2013 ) for a detailed treatment of these notions within the general framework of Inferential Models , which admits a CD as a very specific case. We only mention here that they show that when \(A=\{\theta _0\}\) (i.e. a singleton), \(\text{ bel}_\textbf{x}(\{\theta _0\})=0\) , but \(\text{ bel}_\textbf{x}(\{\theta _0\}^c)\) can be different from 1. In particular, for the normal model N \((\theta ,1)\) , they found that, under some assumptions, \(\text{ bel}_\textbf{x}(\{\theta _0\}^c) =|2\Phi (x-\theta _0)-1|\) . Recalling the definition of the CC and the CD provided in Example 1 , it follows that the plausibility of \(\theta _0\) is \(\text {pl}_\textbf{x}(\{\theta _0\})=1-\text{ bel}_\textbf{x}(\{\theta _0\}^c)=1-|2\Phi (x-\theta _0)-1|= 1-CC_\textbf{x}(\theta _0)\) , and using ( 4 ), we can conclude that the CD*-support of \(\theta _0\) corresponds to half their plausibility.

The CD*-support for a precise hypothesis \({{{\mathcal {H}}}_{0}}: \theta =\theta _0\) is related to the notion of evidence, as defined in a Bayesian context by Pereira et al. ( 2008 ). Evidence is the posterior probability of the set \(\{\theta \in \Theta : p(\theta |\textbf{x})<p(\theta _0|\textbf{x})\}\) , where \(p(\theta |\textbf{x})\) is the posterior density of \(\theta \) . In particular, when a unimodal and symmetric CD is used as a posterior distribution, it is easy to check that the CD*-support coincides with half of the evidence.

The CD*-support is also related to the notion of weak-support defined by Singh et al. ( 2007 ) as \(\sup _{\theta \in [\theta _1,\theta _2]} 2 \min \{H_{\textbf{x}}(\theta ), 1-H_{\textbf{x}}(\theta )\}\) , but important differences exist. If data give little support to \({{{\mathcal {H}}}_{0}}\) , our definition highlights better whether values of \(\theta \) on the right or on the left of \({{{\mathcal {H}}}_{0}}\) are more reasonable. Moreover, if \({{{\mathcal {H}}}_{0}}\) is highly supported, that is \(\theta _m \in [\theta _1,\theta _2]\) , the weak-support is always equal to one, while the CD*-support assumes values in the interval [0.5, 1], allowing to better discriminate between different cases. Only if \({{{\mathcal {H}}}_{0}}\) is a precise hypothesis the two definitions agree, leaving out the multiplicative constant of two.

There exists a strong connection between the CD*-support and the e-value introduced by Peskun ( 2020 ). Under certain regularity assumptions, the e -value can be expressed in terms of a CD and coincides with the CD*-support, so that the properties and results originally established by Peskun for the e -value also apply to the CD*-support. More precisely, let us first consider the case of an observation x generated by the normal model \(\text {N}(\mu ,1)\) . Peskun shows that for the hypothesis \({{{\mathcal {H}}}_{0}}: \mu \in [\mu _1,\mu _2]\) , the e -value is equal to \(\min \{\Phi (x-\mu _1), \Phi (\mu _2-x)\}\) . Since, as shown in Example 1 , \(H_x(\mu )=1-\Phi (x-\mu )=\Phi (\mu -x)\) , it immediately follows that \(\min \{H_x(\mu _2),1-H_x(\mu _1)\}= \min \{\Phi (\mu _2-x), \Phi (x-\mu _1)\}\) , so that the e -value and the CD*-support coincide. For a more general case, we present the following result.

Proposition 4

Let \(\textbf{X}\) be a random vector distributed according to the family of densities \(\{p_\theta , \theta \in \Theta \subseteq \mathbb {R}\}\) with a MLR in the real continuous statistic \(T=T(\textbf{X})\) , with distribution function \(F_\theta (t)\) . If \(F_\theta (t)\) is continuous in \(\theta \) with limits 0 and 1 for \(\theta \) tending to \(\sup (\Theta )\) and \(\inf (\Theta )\) , respectively, then the CD*-support and the e -value for the hypothesis \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) , \(\theta _1 \le \theta _2\) , are equivalent.

We emphasize, however, that the advantage of the CD*-support over the e -value relies on the fact that knowledge of the entire CD allows us to naturally encompass the testing problem into a more comprehensive and coherent inferential framework, in which the e -value is only one of the aspects to be taken into consideration.

Suppose now that a test of significance for \({{\mathcal {H}}}_0: \theta \in [\theta _1,\theta _2]\) , with \(\theta _1 \le \theta _2\) , is desired and that the CD for \(\theta \) is \(H_t(\theta )\) . Recall that the CD-support for \({{{\mathcal {H}}}_{0}}\) is \(H_t([\theta _1,\theta _2]) = \int _{\theta _1}^{\theta _2} dH_{t}(\theta ) = H_t(\theta _2)-H_t(\theta _1)\) , and that when \(\theta _1=\theta _2=\theta _0\) , or the interval \([\theta _1,\theta _2]\) is “small”, it becomes ineffective, and the CD*-support must be employed. The following proposition establishes some results about the CD- and the CD*-tests.

Proposition 5

Given a statistical model parameterized by the real parameter \(\theta \) with MLR in the continuous statistic T , consider the hypothesis \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) with \( \theta _1 \le \theta _2\) . Then,

both the CD- and the CD*-tests reject \({{{\mathcal {H}}}_{0}}\) for all values of T that are smaller or larger than suitable values;

if a threshold \(\gamma \) is fixed for the CD-test, its size is not less than \(\gamma \) ;

for a precise hypothesis, i.e., \(\theta _1=\theta _2\) , the CD*-support, seen as function of the random variable T , has the uniform distribution on (0, 0.5);

if a threshold \(\gamma ^*\) is fixed for the CD*-test, its size falls within the interval \([\gamma ^*, \min (2\gamma ^*,1)]\) and equals \(\min (2\gamma ^*,1)\) when \(\theta _1=\theta _2\) , (i.e. when \({{{\mathcal {H}}}_{0}}\) is a precise hypothesis);

the CD-support is never greater than the CD*-support, and if a common threshold is fixed for both tests, the size of the CD-test is not smaller than that of the CD*-test.

Point i) highlights that the rejection regions generated by the CD- and CD*-tests are two-sided, resembling standard tests for hypotheses of this kind. However, even when \(\gamma = \gamma ^*\) , the rejection regions differ, with the CD-test being more conservative for \({{{\mathcal {H}}}_{0}}\) . This becomes crucial for small intervals, where the CD-test tends to reject the null hypothesis almost invariably.

Under the assumption of Proposition 5 , the p -value corresponding to the commonly used equal tailed test for a precise hypothesis \({{{\mathcal {H}}}_{0}}:\theta =\theta _0\) is \(2\min \{F_{\theta _0}(t), 1-F_{\theta _0}(t)\}\) , so that it coincides with 2 times the CD*-support.

For interval hypotheses, a UMPU test essentially exists only for models within a NEF, and an interesting relationship can be established with the CD-test.

Proposition 6

Given the CD based on the sufficient statistic of a continuous real NEF with natural parameter \(\theta \) , consider the hypothesis \({{\mathcal {H}}}_0: \theta \in [\theta _1,\theta _2]\) versus \({{\mathcal {H}}}_1: \theta \notin [\theta _1,\theta _2]\) , with \(\theta _1 < \theta _2\) . If the CD-test has size \(\alpha _{CD}\) , it is the UMPU test among all \(\alpha _{CD}\) -level tests.

For interval hypotheses, unlike one-sided hypotheses, when the statistic T is discrete, there is no clear reason to prefer either \(H_t^{\ell }\) or \(H_t^r\) . Neither test is more conservative, as their respective rejection regions are shifted by just one point in the support of T . Thus, \(H^g_t\) can be considered again a reasonable compromise, due to its greater proximity to the uniform distribution. Moreover, while the results stated for continuous statistics may not hold exactly for discrete statistics, they remain approximately valid for not too small sample sizes, thanks to the asymptotic normality of CDs, as stated in Proposition 1 .

6 Conclusions

In this article, we propose the use of confidence distributions to address a hypothesis testing problem concerning a real parameter of interest. Specifically, we introduce the CD- and CD*-supports, which are suitable for evaluating one-sided or large interval null hypotheses and precise or small interval null hypotheses, respectively. This approach does not necessarily require identifying the first and second type errors or fixing a significance level a priori. We do not propose an automatic procedure; instead, we suggest a careful and more general inferential analysis of the problem based on CDs. CD- and CD*-supports are two simple coherent measures of evidence for a hypothesis with a clear meaning and interpretation. None of these features are owned by the p -value, which is more complex and generally does not exist in closed form for interval hypothesis.

It is well known that the significance level \(\alpha \) of a test, which is crucial to take a decision, should be adjusted according to the sample size, but this is almost never done in practice. In our approach, the support provided by the CD to a hypothesis trivially depends on the sample size through the dispersion of the CD. For example, if \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) , you can easily observe the effect of sample size on the CD-support of \({{{\mathcal {H}}}_{0}}\) by examining the interval \([\theta _1, \theta _2]\) on the CD-density plot. The CD-support can be non-negligible also when the length \(\Delta =\theta _2-\theta _1\) is small for a CD that is sufficiently concentrated on the interval. The relationship between \(\Delta \) and the dispersion of the CD highlights again the importance of a thoughtful choice of the threshold used for decision-making and the unreasonableness of using standard values. Note that the CD- and CD*-tests are similar in many standard situations, as shown in the examples presented.

Finally, we have investigated some theoretical aspects of the CD- and CD*-tests which are crucial in standard approach. While for one-sided hypotheses, an agreement with standard tests can be established, there are some distinctions to be made for two-sided hypotheses. If a threshold \(\gamma \) is fixed for a CD- or CD*-test, then its size exceeds \(\gamma \) reaching \(2\gamma \) for a CD*-test relative to a precise hypothesis. This is because the CD*-support only considers the appropriate tail suggested by the data and it does not adhere to the typical procedure of doubling the one-sided p -value, a procedure that can be criticized, as seen in Sect. 1 . Of course, if one is convinced of the need to double the p -value, in our context, it is sufficient to double the CD*-support. In the case of a precise hypothesis \({{{\mathcal {H}}}_{0}}: \theta = \theta _0\) , this leads to a valid test because \(Pr_{\theta _0}\left( 2\min \{H_{\textbf{x}}(\theta _0),1-H_{\textbf{x}}(\theta _0)\}\le \alpha \right) \le \alpha \) , as can be deduced by considering the relationship of the CD*-support with the e -value and the results in Peskun ( 2020 , Sec. 2).

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Acknowledgements

Partial financial support was received from Bocconi University. The authors would like to thank the referees for their valuable comments, suggestions and references, which led to a significantly improved version of the manuscript

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Eugenio Melilli & Piero Veronese

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Appendix A. Table of confidence distributions

Appendix b. proof of propositions, proof of proposition 1.

The asymptotic normality and the consistency of the CD in i) and ii) follow from Veronese & Melilli ( 2015 , Thm. 3) for models belonging to a NEF and from Veronese & Melilli ( 2018b , Thm. 1) for continuous arbitrary models. Part iii) of the proposition follows directly using the Chebyshev’s inequality. \(\diamond \)

Proof of Proposition 2

Denote by \(F_{\theta }(t)\) the distribution function of T , assume that its support \({{\mathcal {T}}}=\{t_1,t_2,\ldots ,t_k\}\) is finite for simplicity and let \(p_j=p_j(\theta )=\text{ Pr}_\theta (T=t_j)\) , \(j=1,2,\ldots ,k\) for a fixed \(\theta \) . Consider the case \(H_t^r(\theta )=1-F_{\theta }(t)\) (if \(H_t^r(\theta )=F_{\theta }(t)\) the proof is similar) so that, for each \(j=2,\ldots ,k\) , \(H_{t_j}^\ell (\theta )=H_{t_{j-1}}^r(\theta )\) and \(H_{t_1}^\ell (\theta )=1\) . The supports of the random variables \(H^r_T(\theta )\) , \(H^\ell _T(\theta )\) and \(H^g_T(\theta )\) are, respectively,

where ( 6 ) holds because \(H^r_{t_j}(\theta )< H^g_{t_j}(\theta ) < H^{\ell }_{t_j}(\theta )\) . The probabilities corresponding to the points included in the three supports are of course the same, that is \(p_k,p_{k-1},\ldots ,p_1\) , in this order, so that \(G^\ell (u) \le u \le G^r(u)\) .

Let \(d(Q,R)=\int |Q(x)-R(x)|dx\) be the distance between the two arbitrary distribution functions Q and R . Denoting \(G^u\) as the uniform distribution function on (0, 1), we have

where the last inequality follows from ( 6 ). Thus, the distance from uniformity of \(H_T^g(\theta )\) is less than that of \(H_T^\ell (\theta )\) and of \(H_T^r(\theta )\) and ( 2 ) is proven. \(\diamond \)

Proof of Proposition 4

Given the statistic T and the hypothesis \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) , the e -value, see Peskun 2020 , equation 12), is \(\min \bigg \{\max _{\theta \in [\theta _1,\theta _2]} F_\theta (t), \max _{\theta \in [\theta _1,\theta _2]} (1-F_\theta (t))\bigg \}\) . Under the assumptions of the proposition, it follows that \(F_t(\theta )\) is monotonically nonincreasing in \(\theta \) for each t (see Section 2 ). As a result, the e -value simplifies to:

where the last expression coincides with the CD*-support of \({{{\mathcal {H}}}_{0}}\) . Note that the same result holds if the MLR is nondecreasing in T ensuring that \(F_t(\theta )\) is monotonically nondecreasing. \(\diamond \)

Proof of Proposition 5

Point i). Consider first the CD-test and let \(g(t)=H_t([\theta _1,\theta _2])=H_t(\theta _2)-H_t(\theta _1)=F_{\theta _1}(t)-F_{\theta _2}(t)\) , which is a nonnegative, continuous function with \(\lim _{t\rightarrow \pm \infty }g(t)=0\) and with derivative \(g^\prime (t)=f_{\theta _1}(t)- f_{\theta _2}(t)\) . Let \(t_0 \in \mathbb {R}\) be a point such that g is nondecreasing for \(t<t_0\) and strictly decreasing for \(t \in (t_0,t_1)\) , for a suitable \(t_1>t_0\) ; the existence of \(t_0\) is guaranteed by the properties of g . It follows that \(g^\prime (t) \ge 0\) for \(t<t_0\) and \(g^\prime (t)<0\) in \((t_0,t_1)\) . We show that \(t_0\) is the unique point at which the function \(g^\prime \) changes sign. Indeed, if \(t_2\) were a point greater than \(t_1\) such that \(g^\prime (t)>0\) for t in a suitable interval \((t_2,t_3)\) , with \(t_3> t_2\) , we would have, in this interval, \(f_{\theta _1}(t)>f_{\theta _2}(t)\) . Since \(f_{\theta _1}(t)<f_{\theta _2}(t)\) for \(t \in (t_0,t_1)\) , this implies \(f_{\theta _2}(t)/f_{\theta _1}(t)>1\) for \(t \in (t_0,t_1)\) and \(f_{\theta _2}(t)/f_{\theta _1}(t)<1\) for \(t \in (t_2,t_3)\) , which contradicts the assumption of the (nondecreasing) MLR in T . Thus, g ( t ) is nondecreasing for \(t<t_0\) and nonincreasing for \(t>t_0\) , and the set \(\{t: H_t([\theta _1,\theta _2])< \gamma \}\) coincides with \( \{t: t<t^\prime \) or \(t>t^{\prime \prime }\}\) for suitable \(t^\prime \) and \(t^{\prime \prime }\) .

Consider now the CD*-test. The corresponding support is \(\min \{H_t(\theta _2), 1-H_t(\theta _1)\}= \min \{1-F_{\theta _2}(t), F_{\theta _1}(t)\}\) , which is a continuous function of t and approaches zero as \(t \rightarrow \pm \infty \) . Moreover, it equals \(F_{\theta _1}(t)\) for \(t\le t^*=\inf \{t: F_{\theta _1}(t)=1-F_{\theta _2}(t)\}\) and \(1-F_{\theta _2}(t)\) for \(t\ge t^*\) . Thus, the function is nondecreasing for \(t \le t^*\) and nonincreasing for \(t \ge t^*\) , and the result is proven.

Point ii). Suppose having observed \(t^\prime = F_{\theta _1}^{-1}(\gamma )\) , then the CD-support for \({{{\mathcal {H}}}_{0}}\) is

so that \(t^\prime \) belongs to the rejection region defined by the threshold \(\gamma \) . Due to the structure of this region specified in point i), all \(t\le t^{\prime }\) belong to it. Now,

because \(F_{\theta }(t) \le F_{\theta _1}(t)\) for each t and \(\theta \in [\theta _1,\theta _2]\) . It follows that the size of the CD-test with threshold \(\gamma \) is not smaller than \(\gamma \) .

Point iii). The result follows from the equality of the CD*-support with the e -value, as stated in Proposition 4 , and the uniformity of the e -value as proven in Peskun ( 2020 , Sec. 2).

Point iv). The size of the CD*-test with threshold \(\gamma ^*\) is the supremum on \([\theta _1,\theta _2]\) of the following probability

under the assumption that \(F_{\theta _1}^{-1}(\gamma ^*) <F_{\theta _2}^{-1}(1-\gamma ^*)\) , otherwise the probability is one. Because \(F_{\theta _2}(t) \le F_{\theta }(t) \le F_{\theta _1}(t)\) for each t and \(\theta \in [\theta _1,\theta _2]\) , it follows that \(F_{\theta }(F_{\theta _1}^{-1}(\gamma ^*)) \le F_{\theta _1}(F_{\theta _1}^{-1}(\gamma ^*))=\gamma ^*\) , and \(F_{\theta }(F_{\theta _2}^{-1}(1-\gamma ^*)) \ge F_{\theta _2}(F_{\theta _2}^{-1}(1-\gamma ^*)) = 1-\gamma ^*\) so that the size is

Finally, if \(\theta =\theta _2\) , from ( 7 ) we have

and thus the size of the CD*-test must be included in the interval \([\gamma ^*,2\gamma ^*]\) , provided that \(2\gamma ^*\) is less than 1. For the case \(\theta _1=\theta _2\) , it follows from ( 7 ) that the size of the CD*-test is \(2\gamma ^*\) .

Point v). Because \(H_t([\theta _1,\theta _2]=H_t(\theta _2)-H_t(\theta _1)\le H_t(\theta _2)\) and also \(H_t(\theta _2)-H_t(\theta _1) \le 1-H_t(\theta _1)\) , recalling Definition 4 , it immediately follows that the CD-support is not greater than the CD*-support. Thus if the same threshold is fixed for the two tests, the rejection region of the CD-test includes that of the CD*-test, and the size of the first test is not smaller than that of the second one. \(\diamond \)

Proof of Proposition 6

Recall from point i) of Proposition 5 , that the CD-test with threshold \(\gamma \) rejects \({{{\mathcal {H}}}_{0}}: \theta \in [\theta _1,\theta _2]\) for values of T less than \(t^\prime \) or greater than \(t^{\prime \prime }\) , with \(t^\prime \) and \(t^{\prime \prime }\) solutions of the equation \(F_{\theta _1}(t)-F_{\theta _2}(t)=\gamma \) . Denoting with \(\pi _{CD}\) its power function, we have

Thus the power function of the CD-test is equal in \(\theta _1\) and \(\theta _2\) and this condition characterizes the UMPU test for the exponential families, see Lehmann & Romano ( 2005 , p. 135). \(\diamond \)

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Melilli, E., Veronese, P. Confidence distributions and hypothesis testing. Stat Papers (2024). https://doi.org/10.1007/s00362-024-01542-4

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Received : 05 April 2023

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DOI : https://doi.org/10.1007/s00362-024-01542-4

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