hypothesis test on the mean

Teach yourself statistics

Hypothesis Test for a Mean

This lesson explains how to conduct a hypothesis test of a mean, when the following conditions are met:

• The sampling method is simple random sampling .
• The sampling distribution is normal or nearly normal.

Generally, the sampling distribution will be approximately normally distributed if any of the following conditions apply.

• The population distribution is normal.
• The population distribution is symmetric , unimodal , without outliers , and the sample size is 15 or less.
• The population distribution is moderately skewed , unimodal, without outliers, and the sample size is between 16 and 40.
• The sample size is greater than 40, without outliers.

This approach consists of four steps: (1) state the hypotheses, (2) formulate an analysis plan, (3) analyze sample data, and (4) interpret results.

State the Hypotheses

Every hypothesis test requires the analyst to state a null hypothesis and an alternative hypothesis . The hypotheses are stated in such a way that they are mutually exclusive. That is, if one is true, the other must be false; and vice versa.

The table below shows three sets of hypotheses. Each makes a statement about how the population mean μ is related to a specified value M . (In the table, the symbol ≠ means " not equal to ".)

The first set of hypotheses (Set 1) is an example of a two-tailed test , since an extreme value on either side of the sampling distribution would cause a researcher to reject the null hypothesis. The other two sets of hypotheses (Sets 2 and 3) are one-tailed tests , since an extreme value on only one side of the sampling distribution would cause a researcher to reject the null hypothesis.

Formulate an Analysis Plan

The analysis plan describes how to use sample data to accept or reject the null hypothesis. It should specify the following elements.

• Significance level. Often, researchers choose significance levels equal to 0.01, 0.05, or 0.10; but any value between 0 and 1 can be used.
• Test method. Use the one-sample t-test to determine whether the hypothesized mean differs significantly from the observed sample mean.

Analyze Sample Data

Using sample data, conduct a one-sample t-test. This involves finding the standard error, degrees of freedom, test statistic, and the P-value associated with the test statistic.

SE = s * sqrt{ ( 1/n ) * [ ( N - n ) / ( N - 1 ) ] }

SE = s / sqrt( n )

• Degrees of freedom. The degrees of freedom (DF) is equal to the sample size (n) minus one. Thus, DF = n - 1.

t = ( x - μ) / SE

• P-value. The P-value is the probability of observing a sample statistic as extreme as the test statistic. Since the test statistic is a t statistic, use the t Distribution Calculator to assess the probability associated with the t statistic, given the degrees of freedom computed above. (See sample problems at the end of this lesson for examples of how this is done.)

Sample Size Calculator

As you probably noticed, the process of hypothesis testing can be complex. When you need to test a hypothesis about a mean score, consider using the Sample Size Calculator. The calculator is fairly easy to use, and it is free. You can find the Sample Size Calculator in Stat Trek's main menu under the Stat Tools tab. Or you can tap the button below.

Interpret Results

If the sample findings are unlikely, given the null hypothesis, the researcher rejects the null hypothesis. Typically, this involves comparing the P-value to the significance level , and rejecting the null hypothesis when the P-value is less than the significance level.

Test Your Understanding

In this section, two sample problems illustrate how to conduct a hypothesis test of a mean score. The first problem involves a two-tailed test; the second problem, a one-tailed test.

Problem 1: Two-Tailed Test

An inventor has developed a new, energy-efficient lawn mower engine. He claims that the engine will run continuously for 5 hours (300 minutes) on a single gallon of regular gasoline. From his stock of 2000 engines, the inventor selects a simple random sample of 50 engines for testing. The engines run for an average of 295 minutes, with a standard deviation of 20 minutes. Test the null hypothesis that the mean run time is 300 minutes against the alternative hypothesis that the mean run time is not 300 minutes. Use a 0.05 level of significance. (Assume that run times for the population of engines are normally distributed.)

Solution: The solution to this problem takes four steps: (1) state the hypotheses, (2) formulate an analysis plan, (3) analyze sample data, and (4) interpret results. We work through those steps below:

Null hypothesis: μ = 300

Alternative hypothesis: μ ≠ 300

• Formulate an analysis plan . For this analysis, the significance level is 0.05. The test method is a one-sample t-test .

SE = s / sqrt(n) = 20 / sqrt(50) = 20/7.07 = 2.83

DF = n - 1 = 50 - 1 = 49

t = ( x - μ) / SE = (295 - 300)/2.83 = -1.77

where s is the standard deviation of the sample, x is the sample mean, μ is the hypothesized population mean, and n is the sample size.

Since we have a two-tailed test , the P-value is the probability that the t statistic having 49 degrees of freedom is less than -1.77 or greater than 1.77. We use the t Distribution Calculator to find P(t < -1.77) is about 0.04.

• If you enter 1.77 as the sample mean in the t Distribution Calculator, you will find the that the P(t < 1.77) is about 0.04. Therefore, P(t >  1.77) is 1 minus 0.96 or 0.04. Thus, the P-value = 0.04 + 0.04 = 0.08.
• Interpret results . Since the P-value (0.08) is greater than the significance level (0.05), we cannot reject the null hypothesis.

Note: If you use this approach on an exam, you may also want to mention why this approach is appropriate. Specifically, the approach is appropriate because the sampling method was simple random sampling, the population was normally distributed, and the sample size was small relative to the population size (less than 5%).

Problem 2: One-Tailed Test

Bon Air Elementary School has 1000 students. The principal of the school thinks that the average IQ of students at Bon Air is at least 110. To prove her point, she administers an IQ test to 20 randomly selected students. Among the sampled students, the average IQ is 108 with a standard deviation of 10. Based on these results, should the principal accept or reject her original hypothesis? Assume a significance level of 0.01. (Assume that test scores in the population of engines are normally distributed.)

Null hypothesis: μ >= 110

Alternative hypothesis: μ < 110

• Formulate an analysis plan . For this analysis, the significance level is 0.01. The test method is a one-sample t-test .

SE = s / sqrt(n) = 10 / sqrt(20) = 10/4.472 = 2.236

DF = n - 1 = 20 - 1 = 19

t = ( x - μ) / SE = (108 - 110)/2.236 = -0.894

Here is the logic of the analysis: Given the alternative hypothesis (μ < 110), we want to know whether the observed sample mean is small enough to cause us to reject the null hypothesis.

The observed sample mean produced a t statistic test statistic of -0.894. We use the t Distribution Calculator to find P(t < -0.894) is about 0.19.

• This means we would expect to find a sample mean of 108 or smaller in 19 percent of our samples, if the true population IQ were 110. Thus the P-value in this analysis is 0.19.
• Interpret results . Since the P-value (0.19) is greater than the significance level (0.01), we cannot reject the null hypothesis.

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8.4.3 Hypothesis Testing for the Mean

$\quad$ $H_0$: $\mu=\mu_0$, $\quad$ $H_1$: $\mu \neq \mu_0$.

$\quad$ $H_0$: $\mu \leq \mu_0$, $\quad$ $H_1$: $\mu > \mu_0$.

$\quad$ $H_0$: $\mu \geq \mu_0$, $\quad$ $H_1$: $\mu \lt \mu_0$.

Two-sided Tests for the Mean:

Therefore, we can suggest the following test. Choose a threshold, and call it $c$. If $|W| \leq c$, accept $H_0$, and if $|W|>c$, accept $H_1$. How do we choose $c$? If $\alpha$ is the required significance level, we must have

• As discussed above, we let \begin{align}%\label{} W(X_1,X_2, \cdots,X_n)=\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}}. \end{align} Note that, assuming $H_0$, $W \sim N(0,1)$. We will choose a threshold, $c$. If $|W| \leq c$, we accept $H_0$, and if $|W|>c$, accept $H_1$. To choose $c$, we let \begin{align} P(|W| > c \; | \; H_0) =\alpha. \end{align} Since the standard normal PDF is symmetric around $0$, we have \begin{align} P(|W| > c \; | \; H_0) = 2 P(W>c | \; H_0). \end{align} Thus, we conclude $P(W>c | \; H_0)=\frac{\alpha}{2}$. Therefore, \begin{align} c=z_{\frac{\alpha}{2}}. \end{align} Therefore, we accept $H_0$ if \begin{align} \left|\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}} \right| \leq z_{\frac{\alpha}{2}}, \end{align} and reject it otherwise.
• We have \begin{align} \beta (\mu) &=P(\textrm{type II error}) = P(\textrm{accept }H_0 \; | \; \mu) \\ &= P\left(\left|\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}} \right| \lt z_{\frac{\alpha}{2}}\; | \; \mu \right). \end{align} If $X_i \sim N(\mu,\sigma^2)$, then $\overline{X} \sim N(\mu, \frac{\sigma^2}{n})$. Thus, \begin{align} \beta (\mu)&=P\left(\left|\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}} \right| \lt z_{\frac{\alpha}{2}}\; | \; \mu \right)\\ &=P\left(\mu_0- z_{\frac{\alpha}{2}} \frac{\sigma}{\sqrt{n}} \leq \overline{X} \leq \mu_0+ z_{\frac{\alpha}{2}} \frac{\sigma}{\sqrt{n}}\right)\\ &=\Phi\left(z_{\frac{\alpha}{2}}+\frac{\mu_0-\mu}{\sigma / \sqrt{n}}\right)-\Phi\left(-z_{\frac{\alpha}{2}}+\frac{\mu_0-\mu}{\sigma / \sqrt{n}}\right). \end{align}
• Let $S^2$ be the sample variance for this random sample. Then, the random variable $W$ defined as \begin{equation} W(X_1,X_2, \cdots, X_n)=\frac{\overline{X}-\mu_0}{S / \sqrt{n}} \end{equation} has a $t$-distribution with $n-1$ degrees of freedom, i.e., $W \sim T(n-1)$. Thus, we can repeat the analysis of Example 8.24 here. The only difference is that we need to replace $\sigma$ by $S$ and $z_{\frac{\alpha}{2}}$ by $t_{\frac{\alpha}{2},n-1}$. Therefore, we accept $H_0$ if \begin{align} |W| \leq t_{\frac{\alpha}{2},n-1}, \end{align} and reject it otherwise. Let us look at a numerical example of this case.

$\quad$ $H_0$: $\mu=170$, $\quad$ $H_1$: $\mu \neq 170$.

• Let's first compute the sample mean and the sample standard deviation. The sample mean is \begin{align}%\label{} \overline{X}&=\frac{X_1+X_2+X_3+X_4+X_5+X_6+X_7+X_8+X_9}{9}\\ &=165.8 \end{align} The sample variance is given by \begin{align}%\label{} {S}^2=\frac{1}{9-1} \sum_{k=1}^9 (X_k-\overline{X})^2&=68.01 \end{align} The sample standard deviation is given by \begin{align}%\label{} S&= \sqrt{S^2}=8.25 \end{align} The following MATLAB code can be used to obtain these values: x=[176.2,157.9,160.1,180.9,165.1,167.2,162.9,155.7,166.2]; m=mean(x); v=var(x); s=std(x); Now, our test statistic is \begin{align} W(X_1,X_2, \cdots, X_9)&=\frac{\overline{X}-\mu_0}{S / \sqrt{n}}\\ &=\frac{165.8-170}{8.25 / 3}=-1.52 \end{align} Thus, $|W|=1.52$. Also, we have \begin{align} t_{\frac{\alpha}{2},n-1} = t_{0.025,8} \approx 2.31 \end{align} The above value can be obtained in MATLAB using the command $\mathtt{tinv(0.975,8)}$. Thus, we conclude \begin{align} |W| \leq t_{\frac{\alpha}{2},n-1}. \end{align} Therefore, we accept $H_0$. In other words, we do not have enough evidence to conclude that the average height in the city is different from the average height in the country.

Let us summarize what we have obtained for the two-sided test for the mean.

One-sided Tests for the Mean:

• As before, we define the test statistic as \begin{align}%\label{} W(X_1,X_2, \cdots,X_n)=\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}}. \end{align} If $H_0$ is true (i.e., $\mu \leq \mu_0$), we expect $\overline{X}$ (and thus $W$) to be relatively small, while if $H_1$ is true, we expect $\overline{X}$ (and thus $W$) to be larger. This suggests the following test: Choose a threshold, and call it $c$. If $W \leq c$, accept $H_0$, and if $W>c$, accept $H_1$. How do we choose $c$? If $\alpha$ is the required significance level, we must have \begin{align} P(\textrm{type I error}) &= P(\textrm{Reject }H_0 \; | \; H_0) \\ &= P(W > c \; | \; \mu \leq \mu_0) \leq \alpha. \end{align} Here, the probability of type I error depends on $\mu$. More specifically, for any $\mu \leq \mu_0$, we can write \begin{align} P(\textrm{type I error} \; | \; \mu) &= P(\textrm{Reject }H_0 \; | \; \mu) \\ &= P(W > c \; | \; \mu)\\ &=P \left(\frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}}> c \; | \; \mu\right)\\ &=P \left(\frac{\overline{X}-\mu}{\sigma / \sqrt{n}}+\frac{\mu-\mu_0}{\sigma / \sqrt{n}}> c \; | \; \mu\right)\\ &=P \left(\frac{\overline{X}-\mu}{\sigma / \sqrt{n}}> c+\frac{\mu_0-\mu}{\sigma / \sqrt{n}} \; | \; \mu\right)\\ &\leq P \left(\frac{\overline{X}-\mu}{\sigma / \sqrt{n}}> c \; | \; \mu\right) \quad (\textrm{ since }\mu \leq \mu_0)\\ &=1-\Phi(c) \quad \big(\textrm{ since given }\mu, \frac{\overline{X}-\mu}{\sigma / \sqrt{n}} \sim N(0,1) \big). \end{align} Thus, we can choose $\alpha=1-\Phi(c)$, which results in \begin{align} c=z_{\alpha}. \end{align} Therefore, we accept $H_0$ if \begin{align} \frac{\overline{X}-\mu_0}{\sigma / \sqrt{n}} \leq z_{\alpha}, \end{align} and reject it otherwise.

$\quad$ $H_0$: $\mu \geq \mu_0$, $\quad$ $H_1$: $\mu \lt \mu_0$,

Hypothesis tests about the mean

by Marco Taboga , PhD

This lecture explains how to conduct hypothesis tests about the mean of a normal distribution.

We tackle two different cases:

when we know the variance of the distribution, then we use a z-statistic to conduct the test;

when the variance is unknown, then we use the t-statistic.

In each case we derive the power and the size of the test.

We conclude with two solved exercises on size and power.

Table of contents

Known variance: the z-test

The null hypothesis, the test statistic, the critical region, the decision, the power function, the size of the test, how to choose the critical value, unknown variance: the t-test, how to choose the critical values, solved exercises.

The assumptions are the same we made in the lecture on confidence intervals for the mean .

A test of hypothesis based on it is called z-test .

Otherwise, it is not rejected.

We explain how to do this in the page on critical values .

This case is similar to the previous one. The only difference is that we now relax the assumption that the variance of the distribution is known.

The test of hypothesis based on it is called t-test .

Otherwise, we do not reject it.

The page on critical values explains how this equation is solved.

Below you can find some exercises with explained solutions.

Suppose that a statistician observes 100 independent realizations of a normal random variable.

The mean and the variance of the random variable, which the statistician does not know, are equal to 1 and 4 respectively.

Find the probability that the statistician will reject the null hypothesis that the mean is equal to zero if:

she runs a t-test based on the 100 observed realizations;

A statistician observes 100 independent realizations of a normal random variable.

She performs a t-test of the null hypothesis that the mean of the variable is equal to zero.

How to cite

Please cite as:

Taboga, Marco (2021). "Hypothesis tests about the mean", Lectures on probability theory and mathematical statistics. Kindle Direct Publishing. Online appendix. https://www.statlect.com/fundamentals-of-statistics/hypothesis-testing-mean.

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Statistics Tutorial

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

A population mean is an average of value a population.

Hypothesis tests are used to check a claim about the size of that population mean.

Hypothesis Testing a Mean

The following steps are used for a hypothesis test:

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

For example:

• Population : Nobel Prize winners
• Category : Age when they received the prize.

And we want to check the claim:

"The average age of Nobel Prize winners when they received the prize is more than 55"

By taking a sample of 30 randomly selected Nobel Prize winners we could find that:

The mean age in the sample (\(\bar{x}\)) is 62.1

The standard deviation of age in the sample (\(s\)) is 13.46

From this sample data we check the claim with the steps below.

1. Checking the Conditions

The conditions for calculating a confidence interval for a proportion are:

• The sample is randomly selected
• The population data is normally distributed
• Sample size is large enough

A moderately large sample size, like 30, is typically large enough.

In the example, the sample size was 30 and it was randomly selected, so the conditions are fulfilled.

Note: Checking if the data is normally distributed can be done with specialized statistical tests.

2. Defining the Claims

We need to define a null hypothesis (\(H_{0}\)) and an alternative hypothesis (\(H_{1}\)) based on the claim we are checking.

The claim was:

In this case, the parameter is the mean age of Nobel Prize winners when they received the prize (\(\mu\)).

The null and alternative hypothesis are then:

Null hypothesis : The average age was 55.

Alternative hypothesis : The average age was more than 55.

Which can be expressed with symbols as:

\(H_{0}\): \(\mu = 55 \)

\(H_{1}\): \(\mu > 55 \)

This is a ' right tailed' test, because the alternative hypothesis claims that the proportion is more than in the null hypothesis.

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

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3. Deciding the Significance Level

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

4. Calculating 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.

The formula for the test statistic (TS) of a population mean is:

\(\displaystyle \frac{\bar{x} - \mu}{s} \cdot \sqrt{n} \)

\(\bar{x}-\mu\) is the difference between the sample mean (\(\bar{x}\)) and the claimed population mean (\(\mu\)).

\(s\) is the sample standard deviation .

\(n\) is the sample size.

In our example:

The claimed (\(H_{0}\)) population mean (\(\mu\)) was \( 55 \)

The sample mean (\(\bar{x}\)) was \(62.1\)

The sample standard deviation (\(s\)) was \(13.46\)

The sample size (\(n\)) was \(30\)

So the test statistic (TS) is then:

\(\displaystyle \frac{62.1-55}{13.46} \cdot \sqrt{30} = \frac{7.1}{13.46} \cdot \sqrt{30} \approx 0.528 \cdot 5.477 = \underline{2.889}\)

You can also calculate the test statistic using programming language functions:

With Python use the scipy and math libraries to calculate the test statistic.

With R use built-in math and statistics functions to calculate the test statistic.

5. Concluding

There are two main approaches for making the conclusion of a hypothesis test:

• 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.

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

The Critical Value Approach

For the critical value approach we need to find the critical value (CV) of the significance level (\(\alpha\)).

For a population mean test, the critical value (CV) is a T-value from a student's t-distribution .

This critical T-value (CV) defines the rejection region for the test.

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

Because the claim is that the population mean is more than 55, the rejection region is in the right tail:

The student's t-distribution is adjusted for the uncertainty from smaller samples.

This adjustment is called degrees of freedom (df), which is the sample size \((n) - 1\)

In this case the degrees of freedom (df) is: \(30 - 1 = \underline{29} \)

Choosing a significance level (\(\alpha\)) of 0.01, or 1%, we can find the critical T-value from a T-table , or with a programming language function:

With Python use the Scipy Stats library t.ppf() function find the T-Value for an \(\alpha\) = 0.01 at 29 degrees of freedom (df).

With R use the built-in qt() function to find the t-value for an \(\alpha\) = 0.01 at 29 degrees of freedom (df).

Using either method we can find that the critical T-Value is \(\approx \underline{2.462}\)

For a right tailed test we need to check if the test statistic (TS) is bigger than the critical value (CV).

If the test statistic is bigger than the critical value, the test statistic is in the rejection region .

When the test statistic is in the rejection region, we reject the null hypothesis (\(H_{0}\)).

Here, the test statistic (TS) was \(\approx \underline{2.889}\) and the critical value was \(\approx \underline{2.462}\)

Here is an illustration of this test in a graph:

Since the test statistic was bigger than the critical value we reject the null hypothesis.

This means that the sample data supports the alternative hypothesis.

And we can summarize the conclusion stating:

The sample data supports the claim that "The average age of Nobel Prize winners when they received the prize is more than 55" at a 1% significance level .

The P-Value Approach

For the P-value approach we need to find the P-value of the test statistic (TS).

If the P-value is smaller than the significance level (\(\alpha\)), we reject the null hypothesis (\(H_{0}\)).

The test statistic was found to be \( \approx \underline{2.889} \)

For a population proportion test, the test statistic is a T-Value from a student's t-distribution .

Because this is a right tailed test, we need to find the P-value of a t-value bigger than 2.889.

The student's t-distribution is adjusted according to degrees of freedom (df), which is the sample size \((30) - 1 = \underline{29}\)

We can find the P-value using a T-table , or with a programming language function:

With Python use the Scipy Stats library t.cdf() function find the P-value of a T-value bigger than 2.889 at 29 degrees of freedom (df):

With R use the built-in pt() function find the P-value of a T-Value bigger than 2.889 at 29 degrees of freedom (df):

Using either method we can find that the P-value is \(\approx \underline{0.0036}\)

This tells us that the significance level (\(\alpha\)) would need to be bigger than 0.0036, or 0.36%, to reject the null hypothesis.

This P-value is smaller than any of the common significance levels (10%, 5%, 1%).

So the null hypothesis is rejected at all of these significance levels.

The sample data supports the claim that "The average age of Nobel Prize winners when they received the prize is more than 55" at a 10%, 5%, or 1% significance level .

Note: An outcome of an hypothesis test that rejects the null hypothesis with a p-value of 0.36% means:

For this p-value, we only expect to reject a true null hypothesis 36 out of 10000 times.

Calculating a P-Value for a Hypothesis Test with Programming

Many programming languages can calculate the P-value to decide outcome of a hypothesis test.

Using software and programming to calculate statistics is more common for bigger sets of data, as calculating manually becomes difficult.

The P-value calculated here will tell us the lowest possible significance level where the null-hypothesis can be rejected.

With Python use the scipy and math libraries to calculate the P-value for a right tailed hypothesis test for a mean.

Here, the sample size is 30, the sample mean is 62.1, the sample standard deviation is 13.46, and the test is for a mean bigger than 55.

With R use built-in math and statistics functions find the P-value for a right tailed hypothesis test for a mean.

Left-Tailed and Two-Tailed Tests

This was an example of a right tailed test, where the alternative hypothesis claimed that parameter is bigger than the null hypothesis claim.

You can check out an equivalent step-by-step guide for other types here:

• Left-Tailed Test
• Two-Tailed Test

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Hypothesis Testing for Means & Proportions

Lisa Sullivan, PhD

Professor of Biostatistics

Boston University School of Public Health

Introduction

This is the first of three modules that will addresses the second area of statistical inference, which is hypothesis testing, in which a specific statement or hypothesis is generated about a population parameter, and sample statistics are used to assess the likelihood that the hypothesis is true. The hypothesis is based on available information and the investigator's belief about the population parameters. The process of hypothesis testing involves setting up two competing hypotheses, the null hypothesis and the alternate hypothesis. One selects a random sample (or multiple samples when there are more comparison groups), computes summary statistics and then assesses the likelihood that the sample data support the research or alternative hypothesis. Similar to estimation, the process of hypothesis testing is based on probability theory and the Central Limit Theorem.  

This module will focus on hypothesis testing for means and proportions. The next two modules in this series will address analysis of variance and chi-squared tests. 

Learning Objectives

After completing this module, the student will be able to:

• Define null and research hypothesis, test statistic, level of significance and decision rule
• Distinguish between Type I and Type II errors and discuss the implications of each
• Explain the difference between one and two sided tests of hypothesis
• Estimate and interpret p-values
• Explain the relationship between confidence interval estimates and p-values in drawing inferences
• Differentiate hypothesis testing procedures based on type of outcome variable and number of sample

Introduction to Hypothesis Testing

Techniques for hypothesis testing  .

The techniques for hypothesis testing depend on

• the type of outcome variable being analyzed (continuous, dichotomous, discrete)
• the number of comparison groups in the investigation
• whether the comparison groups are independent (i.e., physically separate such as men versus women) or dependent (i.e., matched or paired such as pre- and post-assessments on the same participants).

In estimation we focused explicitly on techniques for one and two samples and discussed estimation for a specific parameter (e.g., the mean or proportion of a population), for differences (e.g., difference in means, the risk difference) and ratios (e.g., the relative risk and odds ratio). Here we will focus on procedures for one and two samples when the outcome is either continuous (and we focus on means) or dichotomous (and we focus on proportions).

General Approach: A Simple Example

The Centers for Disease Control (CDC) reported on trends in weight, height and body mass index from the 1960's through 2002. 1 The general trend was that Americans were much heavier and slightly taller in 2002 as compared to 1960; both men and women gained approximately 24 pounds, on average, between 1960 and 2002.   In 2002, the mean weight for men was reported at 191 pounds. Suppose that an investigator hypothesizes that weights are even higher in 2006 (i.e., that the trend continued over the subsequent 4 years). The research hypothesis is that the mean weight in men in 2006 is more than 191 pounds. The null hypothesis is that there is no change in weight, and therefore the mean weight is still 191 pounds in 2006.  

In order to test the hypotheses, we select a random sample of American males in 2006 and measure their weights. Suppose we have resources available to recruit n=100 men into our sample. We weigh each participant and compute summary statistics on the sample data. Suppose in the sample we determine the following:

Do the sample data support the null or research hypothesis? The sample mean of 197.1 is numerically higher than 191. However, is this difference more than would be expected by chance? In hypothesis testing, we assume that the null hypothesis holds until proven otherwise. We therefore need to determine the likelihood of observing a sample mean of 197.1 or higher when the true population mean is 191 (i.e., if the null hypothesis is true or under the null hypothesis). We can compute this probability using the Central Limit Theorem. Specifically,

(Notice that we use the sample standard deviation in computing the Z score. This is generally an appropriate substitution as long as the sample size is large, n > 30. Thus, there is less than a 1% probability of observing a sample mean as large as 197.1 when the true population mean is 191. Do you think that the null hypothesis is likely true? Based on how unlikely it is to observe a sample mean of 197.1 under the null hypothesis (i.e., <1% probability), we might infer, from our data, that the null hypothesis is probably not true.

Suppose that the sample data had turned out differently. Suppose that we instead observed the following in 2006:

How likely it is to observe a sample mean of 192.1 or higher when the true population mean is 191 (i.e., if the null hypothesis is true)? We can again compute this probability using the Central Limit Theorem. Specifically,

There is a 33.4% probability of observing a sample mean as large as 192.1 when the true population mean is 191. Do you think that the null hypothesis is likely true?  

Neither of the sample means that we obtained allows us to know with certainty whether the null hypothesis is true or not. However, our computations suggest that, if the null hypothesis were true, the probability of observing a sample mean >197.1 is less than 1%. In contrast, if the null hypothesis were true, the probability of observing a sample mean >192.1 is about 33%. We can't know whether the null hypothesis is true, but the sample that provided a mean value of 197.1 provides much stronger evidence in favor of rejecting the null hypothesis, than the sample that provided a mean value of 192.1. Note that this does not mean that a sample mean of 192.1 indicates that the null hypothesis is true; it just doesn't provide compelling evidence to reject it.

In essence, hypothesis testing is a procedure to compute a probability that reflects the strength of the evidence (based on a given sample) for rejecting the null hypothesis. In hypothesis testing, we determine a threshold or cut-off point (called the critical value) to decide when to believe the null hypothesis and when to believe the research hypothesis. It is important to note that it is possible to observe any sample mean when the true population mean is true (in this example equal to 191), but some sample means are very unlikely. Based on the two samples above it would seem reasonable to believe the research hypothesis when x̄ = 197.1, but to believe the null hypothesis when x̄ =192.1. What we need is a threshold value such that if x̄ is above that threshold then we believe that H 1 is true and if x̄ is below that threshold then we believe that H 0 is true. The difficulty in determining a threshold for x̄ is that it depends on the scale of measurement. In this example, the threshold, sometimes called the critical value, might be 195 (i.e., if the sample mean is 195 or more then we believe that H 1 is true and if the sample mean is less than 195 then we believe that H 0 is true). Suppose we are interested in assessing an increase in blood pressure over time, the critical value will be different because blood pressures are measured in millimeters of mercury (mmHg) as opposed to in pounds. In the following we will explain how the critical value is determined and how we handle the issue of scale.

First, to address the issue of scale in determining the critical value, we convert our sample data (in particular the sample mean) into a Z score. We know from the module on probability that the center of the Z distribution is zero and extreme values are those that exceed 2 or fall below -2. Z scores above 2 and below -2 represent approximately 5% of all Z values. If the observed sample mean is close to the mean specified in H 0 (here m =191), then Z will be close to zero. If the observed sample mean is much larger than the mean specified in H 0 , then Z will be large.  

In hypothesis testing, we select a critical value from the Z distribution. This is done by first determining what is called the level of significance, denoted α ("alpha"). What we are doing here is drawing a line at extreme values. The level of significance is the probability that we reject the null hypothesis (in favor of the alternative) when it is actually true and is also called the Type I error rate.

α = Level of significance = P(Type I error) = P(Reject H 0 | H 0 is true).

Because α is a probability, it ranges between 0 and 1. The most commonly used value in the medical literature for α is 0.05, or 5%. Thus, if an investigator selects α=0.05, then they are allowing a 5% probability of incorrectly rejecting the null hypothesis in favor of the alternative when the null is in fact true. Depending on the circumstances, one might choose to use a level of significance of 1% or 10%. For example, if an investigator wanted to reject the null only if there were even stronger evidence than that ensured with α=0.05, they could choose a =0.01as their level of significance. The typical values for α are 0.01, 0.05 and 0.10, with α=0.05 the most commonly used value.  

Suppose in our weight study we select α=0.05. We need to determine the value of Z that holds 5% of the values above it (see below).

The critical value of Z for α =0.05 is Z = 1.645 (i.e., 5% of the distribution is above Z=1.645). With this value we can set up what is called our decision rule for the test. The rule is to reject H 0 if the Z score is 1.645 or more.  

With the first sample we have

Because 2.38 > 1.645, we reject the null hypothesis. (The same conclusion can be drawn by comparing the 0.0087 probability of observing a sample mean as extreme as 197.1 to the level of significance of 0.05. If the observed probability is smaller than the level of significance we reject H 0 ). Because the Z score exceeds the critical value, we conclude that the mean weight for men in 2006 is more than 191 pounds, the value reported in 2002. If we observed the second sample (i.e., sample mean =192.1), we would not be able to reject the null hypothesis because the Z score is 0.43 which is not in the rejection region (i.e., the region in the tail end of the curve above 1.645). With the second sample we do not have sufficient evidence (because we set our level of significance at 5%) to conclude that weights have increased. Again, the same conclusion can be reached by comparing probabilities. The probability of observing a sample mean as extreme as 192.1 is 33.4% which is not below our 5% level of significance.

Hypothesis Testing: Upper-, Lower, and Two Tailed Tests

The procedure for hypothesis testing is based on the ideas described above. Specifically, we set up competing hypotheses, select a random sample from the population of interest and compute summary statistics. We then determine whether the sample data supports the null or alternative hypotheses. The procedure can be broken down into the following five steps.  

• Step 1. Set up hypotheses and select the level of significance α.

H 0 : Null hypothesis (no change, no difference);  

H 1 : Research hypothesis (investigator's belief); α =0.05

• Step 2. Select the appropriate test statistic.  

The test statistic is a single number that summarizes the sample information.   An example of a test statistic is the Z statistic computed as follows:

When the sample size is small, we will use t statistics (just as we did when constructing confidence intervals for small samples). As we present each scenario, alternative test statistics are provided along with conditions for their appropriate use.

• Step 3.  Set up decision rule.  

The decision rule is a statement that tells under what circumstances to reject the null hypothesis. The decision rule is based on specific values of the test statistic (e.g., reject H 0 if Z > 1.645). The decision rule for a specific test depends on 3 factors: the research or alternative hypothesis, the test statistic and the level of significance. Each is discussed below.

• The decision rule depends on whether an upper-tailed, lower-tailed, or two-tailed test is proposed. In an upper-tailed test the decision rule has investigators reject H 0 if the test statistic is larger than the critical value. In a lower-tailed test the decision rule has investigators reject H 0 if the test statistic is smaller than the critical value.  In a two-tailed test the decision rule has investigators reject H 0 if the test statistic is extreme, either larger than an upper critical value or smaller than a lower critical value.
• The exact form of the test statistic is also important in determining the decision rule. If the test statistic follows the standard normal distribution (Z), then the decision rule will be based on the standard normal distribution. If the test statistic follows the t distribution, then the decision rule will be based on the t distribution. The appropriate critical value will be selected from the t distribution again depending on the specific alternative hypothesis and the level of significance.  
• The third factor is the level of significance. The level of significance which is selected in Step 1 (e.g., α =0.05) dictates the critical value.   For example, in an upper tailed Z test, if α =0.05 then the critical value is Z=1.645.  

The following figures illustrate the rejection regions defined by the decision rule for upper-, lower- and two-tailed Z tests with α=0.05. Notice that the rejection regions are in the upper, lower and both tails of the curves, respectively. The decision rules are written below each figure.

Rejection Region for Lower-Tailed Z Test (H 1 : μ < μ 0 ) with α =0.05

The decision rule is: Reject H 0 if Z < 1.645.

Rejection Region for Two-Tailed Z Test (H 1 : μ ≠ μ 0 ) with α =0.05

The decision rule is: Reject H 0 if Z < -1.960 or if Z > 1.960.

The complete table of critical values of Z for upper, lower and two-tailed tests can be found in the table of Z values to the right in "Other Resources."

Critical values of t for upper, lower and two-tailed tests can be found in the table of t values in "Other Resources."

• Step 4. Compute the test statistic.  

Here we compute the test statistic by substituting the observed sample data into the test statistic identified in Step 2.

• Step 5. Conclusion.  

The final conclusion is made by comparing the test statistic (which is a summary of the information observed in the sample) to the decision rule. The final conclusion will be either to reject the null hypothesis (because the sample data are very unlikely if the null hypothesis is true) or not to reject the null hypothesis (because the sample data are not very unlikely).  

If the null hypothesis is rejected, then an exact significance level is computed to describe the likelihood of observing the sample data assuming that the null hypothesis is true. The exact level of significance is called the p-value and it will be less than the chosen level of significance if we reject H 0 .

Statistical computing packages provide exact p-values as part of their standard output for hypothesis tests. In fact, when using a statistical computing package, the steps outlined about can be abbreviated. The hypotheses (step 1) should always be set up in advance of any analysis and the significance criterion should also be determined (e.g., α =0.05). Statistical computing packages will produce the test statistic (usually reporting the test statistic as t) and a p-value. The investigator can then determine statistical significance using the following: If p < α then reject H 0 .  

• Step 1. Set up hypotheses and determine level of significance

H 0 : μ = 191 H 1 : μ > 191                 α =0.05

The research hypothesis is that weights have increased, and therefore an upper tailed test is used.

• Step 2. Select the appropriate test statistic.

Because the sample size is large (n > 30) the appropriate test statistic is

• Step 3. Set up decision rule.  

In this example, we are performing an upper tailed test (H 1 : μ> 191), with a Z test statistic and selected α =0.05.   Reject H 0 if Z > 1.645.

We now substitute the sample data into the formula for the test statistic identified in Step 2.  

We reject H 0 because 2.38 > 1.645. We have statistically significant evidence at a =0.05, to show that the mean weight in men in 2006 is more than 191 pounds. Because we rejected the null hypothesis, we now approximate the p-value which is the likelihood of observing the sample data if the null hypothesis is true. An alternative definition of the p-value is the smallest level of significance where we can still reject H 0 . In this example, we observed Z=2.38 and for α=0.05, the critical value was 1.645. Because 2.38 exceeded 1.645 we rejected H 0 . In our conclusion we reported a statistically significant increase in mean weight at a 5% level of significance. Using the table of critical values for upper tailed tests, we can approximate the p-value. If we select α=0.025, the critical value is 1.96, and we still reject H 0 because 2.38 > 1.960. If we select α=0.010 the critical value is 2.326, and we still reject H 0 because 2.38 > 2.326. However, if we select α=0.005, the critical value is 2.576, and we cannot reject H 0 because 2.38 < 2.576. Therefore, the smallest α where we still reject H 0 is 0.010. This is the p-value. A statistical computing package would produce a more precise p-value which would be in between 0.005 and 0.010. Here we are approximating the p-value and would report p < 0.010.                  

Type I and Type II Errors

In all tests of hypothesis, there are two types of errors that can be committed. The first is called a Type I error and refers to the situation where we incorrectly reject H 0 when in fact it is true. This is also called a false positive result (as we incorrectly conclude that the research hypothesis is true when in fact it is not). When we run a test of hypothesis and decide to reject H 0 (e.g., because the test statistic exceeds the critical value in an upper tailed test) then either we make a correct decision because the research hypothesis is true or we commit a Type I error. The different conclusions are summarized in the table below. Note that we will never know whether the null hypothesis is really true or false (i.e., we will never know which row of the following table reflects reality).

Table - Conclusions in Test of Hypothesis

In the first step of the hypothesis test, we select a level of significance, α, and α= P(Type I error). Because we purposely select a small value for α, we control the probability of committing a Type I error. For example, if we select α=0.05, and our test tells us to reject H 0 , then there is a 5% probability that we commit a Type I error. Most investigators are very comfortable with this and are confident when rejecting H 0 that the research hypothesis is true (as it is the more likely scenario when we reject H 0 ).

When we run a test of hypothesis and decide not to reject H 0 (e.g., because the test statistic is below the critical value in an upper tailed test) then either we make a correct decision because the null hypothesis is true or we commit a Type II error. Beta (β) represents the probability of a Type II error and is defined as follows: β=P(Type II error) = P(Do not Reject H 0 | H 0 is false). Unfortunately, we cannot choose β to be small (e.g., 0.05) to control the probability of committing a Type II error because β depends on several factors including the sample size, α, and the research hypothesis. When we do not reject H 0 , it may be very likely that we are committing a Type II error (i.e., failing to reject H 0 when in fact it is false). Therefore, when tests are run and the null hypothesis is not rejected we often make a weak concluding statement allowing for the possibility that we might be committing a Type II error. If we do not reject H 0 , we conclude that we do not have significant evidence to show that H 1 is true. We do not conclude that H 0 is true.

 The most common reason for a Type II error is a small sample size.

Tests with One Sample, Continuous Outcome

Hypothesis testing applications with a continuous outcome variable in a single population are performed according to the five-step procedure outlined above. A key component is setting up the null and research hypotheses. The objective is to compare the mean in a single population to known mean (μ 0 ). The known value is generally derived from another study or report, for example a study in a similar, but not identical, population or a study performed some years ago. The latter is called a historical control. It is important in setting up the hypotheses in a one sample test that the mean specified in the null hypothesis is a fair and reasonable comparator. This will be discussed in the examples that follow.

Test Statistics for Testing H 0 : μ= μ 0

• if n > 30
• if n < 30

Note that statistical computing packages will use the t statistic exclusively and make the necessary adjustments for comparing the test statistic to appropriate values from probability tables to produce a p-value. 

The National Center for Health Statistics (NCHS) published a report in 2005 entitled Health, United States, containing extensive information on major trends in the health of Americans. Data are provided for the US population as a whole and for specific ages, sexes and races.  The NCHS report indicated that in 2002 Americans paid an average of $3,302 per year on health care and prescription drugs. An investigator hypothesizes that in 2005 expenditures have decreased primarily due to the availability of generic drugs. To test the hypothesis, a sample of 100 Americans are selected and their expenditures on health care and prescription drugs in 2005 are measured.   The sample data are summarized as follows: n=100, x̄

=$3,190 and s=$890. Is there statistical evidence of a reduction in expenditures on health care and prescription drugs in 2005? Is the sample mean of $3,190 evidence of a true reduction in the mean or is it within chance fluctuation? We will run the test using the five-step approach. 

• Step 1.  Set up hypotheses and determine level of significance

H 0 : μ = 3,302 H 1 : μ < 3,302           α =0.05

The research hypothesis is that expenditures have decreased, and therefore a lower-tailed test is used.

This is a lower tailed test, using a Z statistic and a 5% level of significance.   Reject H 0 if Z < -1.645.

•   Step 4. Compute the test statistic.  

We do not reject H 0 because -1.26 > -1.645. We do not have statistically significant evidence at α=0.05 to show that the mean expenditures on health care and prescription drugs are lower in 2005 than the mean of $3,302 reported in 2002.  

Recall that when we fail to reject H 0 in a test of hypothesis that either the null hypothesis is true (here the mean expenditures in 2005 are the same as those in 2002 and equal to $3,302) or we committed a Type II error (i.e., we failed to reject H 0 when in fact it is false). In summarizing this test, we conclude that we do not have sufficient evidence to reject H 0 . We do not conclude that H 0 is true, because there may be a moderate to high probability that we committed a Type II error. It is possible that the sample size is not large enough to detect a difference in mean expenditures.      

The NCHS reported that the mean total cholesterol level in 2002 for all adults was 203. Total cholesterol levels in participants who attended the seventh examination of the Offspring in the Framingham Heart Study are summarized as follows: n=3,310, x̄ =200.3, and s=36.8. Is there statistical evidence of a difference in mean cholesterol levels in the Framingham Offspring?

Here we want to assess whether the sample mean of 200.3 in the Framingham sample is statistically significantly different from 203 (i.e., beyond what we would expect by chance). We will run the test using the five-step approach.

H 0 : μ= 203 H 1 : μ≠ 203                       α=0.05

The research hypothesis is that cholesterol levels are different in the Framingham Offspring, and therefore a two-tailed test is used.

•   Step 3. Set up decision rule.  

This is a two-tailed test, using a Z statistic and a 5% level of significance. Reject H 0 if Z < -1.960 or is Z > 1.960.

We reject H 0 because -4.22 ≤ -1. .960. We have statistically significant evidence at α=0.05 to show that the mean total cholesterol level in the Framingham Offspring is different from the national average of 203 reported in 2002.   Because we reject H 0 , we also approximate a p-value. Using the two-sided significance levels, p < 0.0001.  

Statistical Significance versus Clinical (Practical) Significance

This example raises an important concept of statistical versus clinical or practical significance. From a statistical standpoint, the total cholesterol levels in the Framingham sample are highly statistically significantly different from the national average with p < 0.0001 (i.e., there is less than a 0.01% chance that we are incorrectly rejecting the null hypothesis). However, the sample mean in the Framingham Offspring study is 200.3, less than 3 units different from the national mean of 203. The reason that the data are so highly statistically significant is due to the very large sample size. It is always important to assess both statistical and clinical significance of data. This is particularly relevant when the sample size is large. Is a 3 unit difference in total cholesterol a meaningful difference?  

Consider again the NCHS-reported mean total cholesterol level in 2002 for all adults of 203. Suppose a new drug is proposed to lower total cholesterol. A study is designed to evaluate the efficacy of the drug in lowering cholesterol.   Fifteen patients are enrolled in the study and asked to take the new drug for 6 weeks. At the end of 6 weeks, each patient's total cholesterol level is measured and the sample statistics are as follows:   n=15, x̄ =195.9 and s=28.7. Is there statistical evidence of a reduction in mean total cholesterol in patients after using the new drug for 6 weeks? We will run the test using the five-step approach. 

H 0 : μ= 203 H 1 : μ< 203                   α=0.05

•  Step 2. Select the appropriate test statistic.  

Because the sample size is small (n<30) the appropriate test statistic is

This is a lower tailed test, using a t statistic and a 5% level of significance. In order to determine the critical value of t, we need degrees of freedom, df, defined as df=n-1. In this example df=15-1=14. The critical value for a lower tailed test with df=14 and a =0.05 is -2.145 and the decision rule is as follows:   Reject H 0 if t < -2.145.

We do not reject H 0 because -0.96 > -2.145. We do not have statistically significant evidence at α=0.05 to show that the mean total cholesterol level is lower than the national mean in patients taking the new drug for 6 weeks. Again, because we failed to reject the null hypothesis we make a weaker concluding statement allowing for the possibility that we may have committed a Type II error (i.e., failed to reject H 0 when in fact the drug is efficacious).

This example raises an important issue in terms of study design. In this example we assume in the null hypothesis that the mean cholesterol level is 203. This is taken to be the mean cholesterol level in patients without treatment. Is this an appropriate comparator? Alternative and potentially more efficient study designs to evaluate the effect of the new drug could involve two treatment groups, where one group receives the new drug and the other does not, or we could measure each patient's baseline or pre-treatment cholesterol level and then assess changes from baseline to 6 weeks post-treatment. These designs are also discussed here.

Video - Comparing a Sample Mean to Known Population Mean (8:20)

Link to transcript of the video

Tests with One Sample, Dichotomous Outcome

Hypothesis testing applications with a dichotomous outcome variable in a single population are also performed according to the five-step procedure. Similar to tests for means, a key component is setting up the null and research hypotheses. The objective is to compare the proportion of successes in a single population to a known proportion (p 0 ). That known proportion is generally derived from another study or report and is sometimes called a historical control. It is important in setting up the hypotheses in a one sample test that the proportion specified in the null hypothesis is a fair and reasonable comparator.    

In one sample tests for a dichotomous outcome, we set up our hypotheses against an appropriate comparator. We select a sample and compute descriptive statistics on the sample data. Specifically, we compute the sample size (n) and the sample proportion which is computed by taking the ratio of the number of successes to the sample size,

We then determine the appropriate test statistic (Step 2) for the hypothesis test. The formula for the test statistic is given below.

Test Statistic for Testing H 0 : p = p 0

if min(np 0 , n(1-p 0 )) > 5

The formula above is appropriate for large samples, defined when the smaller of np 0 and n(1-p 0 ) is at least 5. This is similar, but not identical, to the condition required for appropriate use of the confidence interval formula for a population proportion, i.e.,

Here we use the proportion specified in the null hypothesis as the true proportion of successes rather than the sample proportion. If we fail to satisfy the condition, then alternative procedures, called exact methods must be used to test the hypothesis about the population proportion.

Example:  

The NCHS report indicated that in 2002 the prevalence of cigarette smoking among American adults was 21.1%.  Data on prevalent smoking in n=3,536 participants who attended the seventh examination of the Offspring in the Framingham Heart Study indicated that 482/3,536 = 13.6% of the respondents were currently smoking at the time of the exam. Suppose we want to assess whether the prevalence of smoking is lower in the Framingham Offspring sample given the focus on cardiovascular health in that community. Is there evidence of a statistically lower prevalence of smoking in the Framingham Offspring study as compared to the prevalence among all Americans?

H 0 : p = 0.211 H 1 : p < 0.211                     α=0.05

We must first check that the sample size is adequate.   Specifically, we need to check min(np 0 , n(1-p 0 )) = min( 3,536(0.211), 3,536(1-0.211))=min(746, 2790)=746. The sample size is more than adequate so the following formula can be used:

This is a lower tailed test, using a Z statistic and a 5% level of significance. Reject H 0 if Z < -1.645.

We reject H 0 because -10.93 < -1.645. We have statistically significant evidence at α=0.05 to show that the prevalence of smoking in the Framingham Offspring is lower than the prevalence nationally (21.1%). Here, p < 0.0001.  

The NCHS report indicated that in 2002, 75% of children aged 2 to 17 saw a dentist in the past year. An investigator wants to assess whether use of dental services is similar in children living in the city of Boston. A sample of 125 children aged 2 to 17 living in Boston are surveyed and 64 reported seeing a dentist over the past 12 months. Is there a significant difference in use of dental services between children living in Boston and the national data?

Calculate this on your own before checking the answer.

Video - Hypothesis Test for One Sample and a Dichotomous Outcome (3:55)

Tests with Two Independent Samples, Continuous Outcome

There are many applications where it is of interest to compare two independent groups with respect to their mean scores on a continuous outcome. Here we compare means between groups, but rather than generating an estimate of the difference, we will test whether the observed difference (increase, decrease or difference) is statistically significant or not. Remember, that hypothesis testing gives an assessment of statistical significance, whereas estimation gives an estimate of effect and both are important.

Here we discuss the comparison of means when the two comparison groups are independent or physically separate. The two groups might be determined by a particular attribute (e.g., sex, diagnosis of cardiovascular disease) or might be set up by the investigator (e.g., participants assigned to receive an experimental treatment or placebo). The first step in the analysis involves computing descriptive statistics on each of the two samples. Specifically, we compute the sample size, mean and standard deviation in each sample and we denote these summary statistics as follows:

for sample 1:

for sample 2:

The designation of sample 1 and sample 2 is arbitrary. In a clinical trial setting the convention is to call the treatment group 1 and the control group 2. However, when comparing men and women, for example, either group can be 1 or 2.  

In the two independent samples application with a continuous outcome, the parameter of interest in the test of hypothesis is the difference in population means, μ 1 -μ 2 . The null hypothesis is always that there is no difference between groups with respect to means, i.e.,

The null hypothesis can also be written as follows: H 0 : μ 1 = μ 2 . In the research hypothesis, an investigator can hypothesize that the first mean is larger than the second (H 1 : μ 1 > μ 2 ), that the first mean is smaller than the second (H 1 : μ 1 < μ 2 ), or that the means are different (H 1 : μ 1 ≠ μ 2 ). The three different alternatives represent upper-, lower-, and two-tailed tests, respectively. The following test statistics are used to test these hypotheses.

Test Statistics for Testing H 0 : μ 1 = μ 2

• if n 1 > 30 and n 2 > 30
• if n 1 < 30 or n 2 < 30

NOTE: The formulas above assume equal variability in the two populations (i.e., the population variances are equal, or s 1 2 = s 2 2 ). This means that the outcome is equally variable in each of the comparison populations. For analysis, we have samples from each of the comparison populations. If the sample variances are similar, then the assumption about variability in the populations is probably reasonable. As a guideline, if the ratio of the sample variances, s 1 2 /s 2 2 is between 0.5 and 2 (i.e., if one variance is no more than double the other), then the formulas above are appropriate. If the ratio of the sample variances is greater than 2 or less than 0.5 then alternative formulas must be used to account for the heterogeneity in variances.    

The test statistics include Sp, which is the pooled estimate of the common standard deviation (again assuming that the variances in the populations are similar) computed as the weighted average of the standard deviations in the samples as follows:

Because we are assuming equal variances between groups, we pool the information on variability (sample variances) to generate an estimate of the variability in the population. Note: Because Sp is a weighted average of the standard deviations in the sample, Sp will always be in between s 1 and s 2 .)

Data measured on n=3,539 participants who attended the seventh examination of the Offspring in the Framingham Heart Study are shown below.  

Suppose we now wish to assess whether there is a statistically significant difference in mean systolic blood pressures between men and women using a 5% level of significance.  

H 0 : μ 1 = μ 2

H 1 : μ 1 ≠ μ 2                       α=0.05

Because both samples are large ( > 30), we can use the Z test statistic as opposed to t. Note that statistical computing packages use t throughout. Before implementing the formula, we first check whether the assumption of equality of population variances is reasonable. The guideline suggests investigating the ratio of the sample variances, s 1 2 /s 2 2 . Suppose we call the men group 1 and the women group 2. Again, this is arbitrary; it only needs to be noted when interpreting the results. The ratio of the sample variances is 17.5 2 /20.1 2 = 0.76, which falls between 0.5 and 2 suggesting that the assumption of equality of population variances is reasonable. The appropriate test statistic is

We now substitute the sample data into the formula for the test statistic identified in Step 2. Before substituting, we will first compute Sp, the pooled estimate of the common standard deviation.

Notice that the pooled estimate of the common standard deviation, Sp, falls in between the standard deviations in the comparison groups (i.e., 17.5 and 20.1). Sp is slightly closer in value to the standard deviation in the women (20.1) as there were slightly more women in the sample.   Recall, Sp is a weight average of the standard deviations in the comparison groups, weighted by the respective sample sizes.  

Now the test statistic:

We reject H 0 because 2.66 > 1.960. We have statistically significant evidence at α=0.05 to show that there is a difference in mean systolic blood pressures between men and women. The p-value is p < 0.010.  

Here again we find that there is a statistically significant difference in mean systolic blood pressures between men and women at p < 0.010. Notice that there is a very small difference in the sample means (128.2-126.5 = 1.7 units), but this difference is beyond what would be expected by chance. Is this a clinically meaningful difference? The large sample size in this example is driving the statistical significance. A 95% confidence interval for the difference in mean systolic blood pressures is: 1.7 + 1.26 or (0.44, 2.96). The confidence interval provides an assessment of the magnitude of the difference between means whereas the test of hypothesis and p-value provide an assessment of the statistical significance of the difference.  

Above we performed a study to evaluate a new drug designed to lower total cholesterol. The study involved one sample of patients, each patient took the new drug for 6 weeks and had their cholesterol measured. As a means of evaluating the efficacy of the new drug, the mean total cholesterol following 6 weeks of treatment was compared to the NCHS-reported mean total cholesterol level in 2002 for all adults of 203. At the end of the example, we discussed the appropriateness of the fixed comparator as well as an alternative study design to evaluate the effect of the new drug involving two treatment groups, where one group receives the new drug and the other does not. Here, we revisit the example with a concurrent or parallel control group, which is very typical in randomized controlled trials or clinical trials (refer to the EP713 module on Clinical Trials).  

A new drug is proposed to lower total cholesterol. A randomized controlled trial is designed to evaluate the efficacy of the medication in lowering cholesterol. Thirty participants are enrolled in the trial and are randomly assigned to receive either the new drug or a placebo. The participants do not know which treatment they are assigned. Each participant is asked to take the assigned treatment for 6 weeks. At the end of 6 weeks, each patient's total cholesterol level is measured and the sample statistics are as follows.

Is there statistical evidence of a reduction in mean total cholesterol in patients taking the new drug for 6 weeks as compared to participants taking placebo? We will run the test using the five-step approach.

H 0 : μ 1 = μ 2 H 1 : μ 1 < μ 2                         α=0.05

Because both samples are small (< 30), we use the t test statistic. Before implementing the formula, we first check whether the assumption of equality of population variances is reasonable. The ratio of the sample variances, s 1 2 /s 2 2 =28.7 2 /30.3 2 = 0.90, which falls between 0.5 and 2, suggesting that the assumption of equality of population variances is reasonable. The appropriate test statistic is:

This is a lower-tailed test, using a t statistic and a 5% level of significance. The appropriate critical value can be found in the t Table (in More Resources to the right). In order to determine the critical value of t we need degrees of freedom, df, defined as df=n 1 +n 2 -2 = 15+15-2=28. The critical value for a lower tailed test with df=28 and α=0.05 is -1.701 and the decision rule is: Reject H 0 if t < -1.701.

Now the test statistic,

We reject H 0 because -2.92 < -1.701. We have statistically significant evidence at α=0.05 to show that the mean total cholesterol level is lower in patients taking the new drug for 6 weeks as compared to patients taking placebo, p < 0.005.

The clinical trial in this example finds a statistically significant reduction in total cholesterol, whereas in the previous example where we had a historical control (as opposed to a parallel control group) we did not demonstrate efficacy of the new drug. Notice that the mean total cholesterol level in patients taking placebo is 217.4 which is very different from the mean cholesterol reported among all Americans in 2002 of 203 and used as the comparator in the prior example. The historical control value may not have been the most appropriate comparator as cholesterol levels have been increasing over time. In the next section, we present another design that can be used to assess the efficacy of the new drug.

Video - Comparison of Two Independent Samples With a Continuous Outcome (8:02)

Tests with Matched Samples, Continuous Outcome

In the previous section we compared two groups with respect to their mean scores on a continuous outcome. An alternative study design is to compare matched or paired samples. The two comparison groups are said to be dependent, and the data can arise from a single sample of participants where each participant is measured twice (possibly before and after an intervention) or from two samples that are matched on specific characteristics (e.g., siblings). When the samples are dependent, we focus on difference scores in each participant or between members of a pair and the test of hypothesis is based on the mean difference, μ d . The null hypothesis again reflects "no difference" and is stated as H 0 : μ d =0 . Note that there are some instances where it is of interest to test whether there is a difference of a particular magnitude (e.g., μ d =5) but in most instances the null hypothesis reflects no difference (i.e., μ d =0).  

The appropriate formula for the test of hypothesis depends on the sample size. The formulas are shown below and are identical to those we presented for estimating the mean of a single sample presented (e.g., when comparing against an external or historical control), except here we focus on difference scores.

Test Statistics for Testing H 0 : μ d =0

A new drug is proposed to lower total cholesterol and a study is designed to evaluate the efficacy of the drug in lowering cholesterol. Fifteen patients agree to participate in the study and each is asked to take the new drug for 6 weeks. However, before starting the treatment, each patient's total cholesterol level is measured. The initial measurement is a pre-treatment or baseline value. After taking the drug for 6 weeks, each patient's total cholesterol level is measured again and the data are shown below. The rightmost column contains difference scores for each patient, computed by subtracting the 6 week cholesterol level from the baseline level. The differences represent the reduction in total cholesterol over 4 weeks. (The differences could have been computed by subtracting the baseline total cholesterol level from the level measured at 6 weeks. The way in which the differences are computed does not affect the outcome of the analysis only the interpretation.)

Because the differences are computed by subtracting the cholesterols measured at 6 weeks from the baseline values, positive differences indicate reductions and negative differences indicate increases (e.g., participant 12 increases by 2 units over 6 weeks). The goal here is to test whether there is a statistically significant reduction in cholesterol. Because of the way in which we computed the differences, we want to look for an increase in the mean difference (i.e., a positive reduction). In order to conduct the test, we need to summarize the differences. In this sample, we have

The calculations are shown below.  

Is there statistical evidence of a reduction in mean total cholesterol in patients after using the new medication for 6 weeks? We will run the test using the five-step approach.

H 0 : μ d = 0 H 1 : μ d > 0                 α=0.05

NOTE: If we had computed differences by subtracting the baseline level from the level measured at 6 weeks then negative differences would have reflected reductions and the research hypothesis would have been H 1 : μ d < 0. 

• Step 2 . Select the appropriate test statistic.

This is an upper-tailed test, using a t statistic and a 5% level of significance. The appropriate critical value can be found in the t Table at the right, with df=15-1=14. The critical value for an upper-tailed test with df=14 and α=0.05 is 2.145 and the decision rule is Reject H 0 if t > 2.145.

We now substitute the sample data into the formula for the test statistic identified in Step 2.

We reject H 0 because 4.61 > 2.145. We have statistically significant evidence at α=0.05 to show that there is a reduction in cholesterol levels over 6 weeks.  

Here we illustrate the use of a matched design to test the efficacy of a new drug to lower total cholesterol. We also considered a parallel design (randomized clinical trial) and a study using a historical comparator. It is extremely important to design studies that are best suited to detect a meaningful difference when one exists. There are often several alternatives and investigators work with biostatisticians to determine the best design for each application. It is worth noting that the matched design used here can be problematic in that observed differences may only reflect a "placebo" effect. All participants took the assigned medication, but is the observed reduction attributable to the medication or a result of these participation in a study.

Video - Hypothesis Testing With a Matched Sample and a Continuous Outcome (3:11)

Tests with Two Independent Samples, Dichotomous Outcome

There are several approaches that can be used to test hypotheses concerning two independent proportions. Here we present one approach - the chi-square test of independence is an alternative, equivalent, and perhaps more popular approach to the same analysis. Hypothesis testing with the chi-square test is addressed in the third module in this series: BS704_HypothesisTesting-ChiSquare.

In tests of hypothesis comparing proportions between two independent groups, one test is performed and results can be interpreted to apply to a risk difference, relative risk or odds ratio. As a reminder, the risk difference is computed by taking the difference in proportions between comparison groups, the risk ratio is computed by taking the ratio of proportions, and the odds ratio is computed by taking the ratio of the odds of success in the comparison groups. Because the null values for the risk difference, the risk ratio and the odds ratio are different, the hypotheses in tests of hypothesis look slightly different depending on which measure is used. When performing tests of hypothesis for the risk difference, relative risk or odds ratio, the convention is to label the exposed or treated group 1 and the unexposed or control group 2.      

For example, suppose a study is designed to assess whether there is a significant difference in proportions in two independent comparison groups. The test of interest is as follows:

H 0 : p 1 = p 2 versus H 1 : p 1 ≠ p 2 .  

The following are the hypothesis for testing for a difference in proportions using the risk difference, the risk ratio and the odds ratio. First, the hypotheses above are equivalent to the following:

• For the risk difference, H 0 : p 1 - p 2 = 0 versus H 1 : p 1 - p 2 ≠ 0 which are, by definition, equal to H 0 : RD = 0 versus H 1 : RD ≠ 0.
• If an investigator wants to focus on the risk ratio, the equivalent hypotheses are H 0 : RR = 1 versus H 1 : RR ≠ 1.
• If the investigator wants to focus on the odds ratio, the equivalent hypotheses are H 0 : OR = 1 versus H 1 : OR ≠ 1.  

Suppose a test is performed to test H 0 : RD = 0 versus H 1 : RD ≠ 0 and the test rejects H 0 at α=0.05. Based on this test we can conclude that there is significant evidence, α=0.05, of a difference in proportions, significant evidence that the risk difference is not zero, significant evidence that the risk ratio and odds ratio are not one. The risk difference is analogous to the difference in means when the outcome is continuous. Here the parameter of interest is the difference in proportions in the population, RD = p 1 -p 2 and the null value for the risk difference is zero. In a test of hypothesis for the risk difference, the null hypothesis is always H 0 : RD = 0. This is equivalent to H 0 : RR = 1 and H 0 : OR = 1. In the research hypothesis, an investigator can hypothesize that the first proportion is larger than the second (H 1 : p 1 > p 2 , which is equivalent to H 1 : RD > 0, H 1 : RR > 1 and H 1 : OR > 1), that the first proportion is smaller than the second (H 1 : p 1 < p 2 , which is equivalent to H 1 : RD < 0, H 1 : RR < 1 and H 1 : OR < 1), or that the proportions are different (H 1 : p 1 ≠ p 2 , which is equivalent to H 1 : RD ≠ 0, H 1 : RR ≠ 1 and H 1 : OR ≠

1). The three different alternatives represent upper-, lower- and two-tailed tests, respectively.  

The formula for the test of hypothesis for the difference in proportions is given below.

Test Statistics for Testing H 0 : p 1 = p

The formula above is appropriate for large samples, defined as at least 5 successes (np > 5) and at least 5 failures (n(1-p > 5)) in each of the two samples. If there are fewer than 5 successes or failures in either comparison group, then alternative procedures, called exact methods must be used to estimate the difference in population proportions.

The following table summarizes data from n=3,799 participants who attended the fifth examination of the Offspring in the Framingham Heart Study. The outcome of interest is prevalent CVD and we want to test whether the prevalence of CVD is significantly higher in smokers as compared to non-smokers.

The prevalence of CVD (or proportion of participants with prevalent CVD) among non-smokers is 298/3,055 = 0.0975 and the prevalence of CVD among current smokers is 81/744 = 0.1089. Here smoking status defines the comparison groups and we will call the current smokers group 1 (exposed) and the non-smokers (unexposed) group 2. The test of hypothesis is conducted below using the five step approach.

H 0 : p 1 = p 2     H 1 : p 1 ≠ p 2                 α=0.05

• Step 2.  Select the appropriate test statistic.  

We must first check that the sample size is adequate. Specifically, we need to ensure that we have at least 5 successes and 5 failures in each comparison group. In this example, we have more than enough successes (cases of prevalent CVD) and failures (persons free of CVD) in each comparison group. The sample size is more than adequate so the following formula can be used:

Reject H 0 if Z < -1.960 or if Z > 1.960.

We now substitute the sample data into the formula for the test statistic identified in Step 2. We first compute the overall proportion of successes:

We now substitute to compute the test statistic.

• Step 5. Conclusion.

We do not reject H 0 because -1.960 < 0.927 < 1.960. We do not have statistically significant evidence at α=0.05 to show that there is a difference in prevalent CVD between smokers and non-smokers.  

A 95% confidence interval for the difference in prevalent CVD (or risk difference) between smokers and non-smokers as 0.0114 + 0.0247, or between -0.0133 and 0.0361. Because the 95% confidence interval for the risk difference includes zero we again conclude that there is no statistically significant difference in prevalent CVD between smokers and non-smokers.    

Smoking has been shown over and over to be a risk factor for cardiovascular disease. What might explain the fact that we did not observe a statistically significant difference using data from the Framingham Heart Study? HINT: Here we consider prevalent CVD, would the results have been different if we considered incident CVD?

A randomized trial is designed to evaluate the effectiveness of a newly developed pain reliever designed to reduce pain in patients following joint replacement surgery. The trial compares the new pain reliever to the pain reliever currently in use (called the standard of care). A total of 100 patients undergoing joint replacement surgery agreed to participate in the trial. Patients were randomly assigned to receive either the new pain reliever or the standard pain reliever following surgery and were blind to the treatment assignment. Before receiving the assigned treatment, patients were asked to rate their pain on a scale of 0-10 with higher scores indicative of more pain. Each patient was then given the assigned treatment and after 30 minutes was again asked to rate their pain on the same scale. The primary outcome was a reduction in pain of 3 or more scale points (defined by clinicians as a clinically meaningful reduction). The following data were observed in the trial.

We now test whether there is a statistically significant difference in the proportions of patients reporting a meaningful reduction (i.e., a reduction of 3 or more scale points) using the five step approach.  

H 0 : p 1 = p 2     H 1 : p 1 ≠ p 2              α=0.05

Here the new or experimental pain reliever is group 1 and the standard pain reliever is group 2.

We must first check that the sample size is adequate. Specifically, we need to ensure that we have at least 5 successes and 5 failures in each comparison group, i.e.,

In this example, we have min(50(0.46), 50(1-0.46), 50(0.22), 50(1-0.22)) = min(23, 27, 11, 39) = 11. The sample size is adequate so the following formula can be used

We reject H 0 because 2.526 > 1960. We have statistically significant evidence at a =0.05 to show that there is a difference in the proportions of patients on the new pain reliever reporting a meaningful reduction (i.e., a reduction of 3 or more scale points) as compared to patients on the standard pain reliever.

A 95% confidence interval for the difference in proportions of patients on the new pain reliever reporting a meaningful reduction (i.e., a reduction of 3 or more scale points) as compared to patients on the standard pain reliever is 0.24 + 0.18 or between 0.06 and 0.42. Because the 95% confidence interval does not include zero we concluded that there was a statistically significant difference in proportions which is consistent with the test of hypothesis result. 

Again, the procedures discussed here apply to applications where there are two independent comparison groups and a dichotomous outcome. There are other applications in which it is of interest to compare a dichotomous outcome in matched or paired samples. For example, in a clinical trial we might wish to test the effectiveness of a new antibiotic eye drop for the treatment of bacterial conjunctivitis. Participants use the new antibiotic eye drop in one eye and a comparator (placebo or active control treatment) in the other. The success of the treatment (yes/no) is recorded for each participant for each eye. Because the two assessments (success or failure) are paired, we cannot use the procedures discussed here. The appropriate test is called McNemar's test (sometimes called McNemar's test for dependent proportions).  

Vide0 - Hypothesis Testing With Two Independent Samples and a Dichotomous Outcome (2:55)

Here we presented hypothesis testing techniques for means and proportions in one and two sample situations. Tests of hypothesis involve several steps, including specifying the null and alternative or research hypothesis, selecting and computing an appropriate test statistic, setting up a decision rule and drawing a conclusion. There are many details to consider in hypothesis testing. The first is to determine the appropriate test. We discussed Z and t tests here for different applications. The appropriate test depends on the distribution of the outcome variable (continuous or dichotomous), the number of comparison groups (one, two) and whether the comparison groups are independent or dependent. The following table summarizes the different tests of hypothesis discussed here.

• Continuous Outcome, One Sample: H0: μ = μ0
• Continuous Outcome, Two Independent Samples: H0: μ1 = μ2
• Continuous Outcome, Two Matched Samples: H0: μd = 0
• Dichotomous Outcome, One Sample: H0: p = p 0
• Dichotomous Outcome, Two Independent Samples: H0: p1 = p2, RD=0, RR=1, OR=1

Once the type of test is determined, the details of the test must be specified. Specifically, the null and alternative hypotheses must be clearly stated. The null hypothesis always reflects the "no change" or "no difference" situation. The alternative or research hypothesis reflects the investigator's belief. The investigator might hypothesize that a parameter (e.g., a mean, proportion, difference in means or proportions) will increase, will decrease or will be different under specific conditions (sometimes the conditions are different experimental conditions and other times the conditions are simply different groups of participants). Once the hypotheses are specified, data are collected and summarized. The appropriate test is then conducted according to the five step approach. If the test leads to rejection of the null hypothesis, an approximate p-value is computed to summarize the significance of the findings. When tests of hypothesis are conducted using statistical computing packages, exact p-values are computed. Because the statistical tables in this textbook are limited, we can only approximate p-values. If the test fails to reject the null hypothesis, then a weaker concluding statement is made for the following reason.

In hypothesis testing, there are two types of errors that can be committed. A Type I error occurs when a test incorrectly rejects the null hypothesis. This is referred to as a false positive result, and the probability that this occurs is equal to the level of significance, α. The investigator chooses the level of significance in Step 1, and purposely chooses a small value such as α=0.05 to control the probability of committing a Type I error. A Type II error occurs when a test fails to reject the null hypothesis when in fact it is false. The probability that this occurs is equal to β. Unfortunately, the investigator cannot specify β at the outset because it depends on several factors including the sample size (smaller samples have higher b), the level of significance (β decreases as a increases), and the difference in the parameter under the null and alternative hypothesis.    

We noted in several examples in this chapter, the relationship between confidence intervals and tests of hypothesis. The approaches are different, yet related. It is possible to draw a conclusion about statistical significance by examining a confidence interval. For example, if a 95% confidence interval does not contain the null value (e.g., zero when analyzing a mean difference or risk difference, one when analyzing relative risks or odds ratios), then one can conclude that a two-sided test of hypothesis would reject the null at α=0.05. It is important to note that the correspondence between a confidence interval and test of hypothesis relates to a two-sided test and that the confidence level corresponds to a specific level of significance (e.g., 95% to α=0.05, 90% to α=0.10 and so on). The exact significance of the test, the p-value, can only be determined using the hypothesis testing approach and the p-value provides an assessment of the strength of the evidence and not an estimate of the effect.

Answers to Selected Problems

Dental services problem - bottom of page 5.

• Step 1: Set up hypotheses and determine the level of significance.

α=0.05

• Step 2: Select the appropriate test statistic.

First, determine whether the sample size is adequate.

Therefore the sample size is adequate, and we can use the following formula:

• Step 3: Set up the decision rule.

Reject H0 if Z is less than or equal to -1.96 or if Z is greater than or equal to 1.96.

• Step 4: Compute the test statistic
• Step 5: Conclusion.

We reject the null hypothesis because -6.15<-1.96. Therefore there is a statistically significant difference in the proportion of children in Boston using dental services compated to the national proportion.

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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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5.3 - hypothesis testing for one-sample mean.

In the previous section, we learned how to perform a hypothesis test for one proportion. The concepts of hypothesis testing remain constant for any hypothesis test. In these next few sections, we will present the hypothesis test for one mean. We start with our knowledge of the sampling distribution of the sample mean.

Hypothesis Test for One-Sample Mean Section  

Recall that under certain conditions, the sampling distribution of the sample mean, \(\bar{x} \), is approximately normal with mean, \(\mu \), standard error \(\dfrac{\sigma}{\sqrt{n}} \), and estimated standard error \(\dfrac{s}{\sqrt{n}} \).

\(H_0\colon \mu=\mu_0\)

Conditions:

• The distribution of the population is Normal
• The sample size is large \( n>30 \).

Test Statistic:

If at least one of conditions are satisfied, then...

\( t=\dfrac{\bar{x}-\mu_0}{\frac{s}{\sqrt{n}}} \)

will follow a t-distribution with \(n-1 \) degrees of freedom.

Notice when working with continuous data we are going to use a t statistic as opposed to the z statistic. This is due to the fact that the sample size impacts the sampling distribution and needs to be taken into account. We do this by recognizing “degrees of freedom”. We will not go into too much detail about degrees of freedom in this course.

Let’s look at an example.

Example 5-1 Section  

This depends on the standard deviation of \(\bar{x} \) . 

\begin{align} t^*&=\dfrac{\bar{x}-\mu}{\frac{s}{\sqrt{n}}}\\&=\dfrac{8.3-8.5}{\frac{1.2}{\sqrt{61}}}\\&=-1.3 \end{align} 

Thus, we are asking if \(-1.3\) is very far away from zero, since that corresponds to the case when \(\bar{x}\) is equal to \(\mu_0 \). If it is far away, then it is unlikely that the null hypothesis is true and one rejects it. Otherwise, one cannot reject the null hypothesis. 

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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Hey there. My name is Zach Bobbitt. I have a Masters of Science degree in Applied Statistics and I’ve worked on machine learning algorithms for professional businesses in both healthcare and retail. I’m passionate about statistics, machine learning, and data visualization and I created Statology to be a resource for both students and teachers alike.  My goal with this site is to help you learn statistics through using simple terms, plenty of real-world examples, and helpful illustrations.

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10.6: Test of Mean vs. Hypothesized Value – A Complete Example

• Last updated
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• Page ID 20909

• Maurice A. Geraghty
• De Anza College

Example – Soy sauce production

A food company has a policy that the stated contents of a product match the actual results. A General Question might be “Does the stated net weight of a food product match the actual weight?” The quality control statistician decides to test the 16 ounce bottle of Soy Sauce and must now design the experiment .

The quality‐control statistician has been given the authority to sample 36 bottles of soy sauce and knows from past testing that the population standard deviation is 0.5 ounces. The model will be a test of population mean vs. hypothesized value of 16 oz.  A two‐tailed test is selected since the company is concerned about both overfilling and underfilling the bottles as the stated policy is that the stated weight should match the actual weight of the product.

Research Hypotheses :

\(H_o: \mu =16\)  (The filling machine is operating properly)                                          

\(H_a: \mu \neq 16\) (The filling machine is not operating properly)

Since the population standard deviation is known the test statistic will be \(Z=\dfrac{\overline{X}-\mu}{\sigma / \sqrt{n}}\). This model is appropriate since the sample size assures that the distribution of the sample mean is approximately Normal due to the Central Limit Theorem.

Type I error would be to reject the Null Hypothesis and say that the machine is not running properly when in fact it was operating properly. Since the company does not want to needlessly stop production and recalibrate the machine, the statistician chooses to limit the probability of Type I error by setting the level of significance (\(\alpha\)) to 5%.

The statistician now conducts the experiment and samples 36 bottles over one hour and determines from a box plot of the data that there is one unusual observation of 17.56 ounces. The value is rechecked and kept in the data set.

Next, the sample mean and the test statistic are calculated.

\[\overline{X}=16.12 \text { ounces } \qquad \qquad Z=\dfrac{16.12-16}{0.5 / \sqrt{36}}=1.44 \nonumber \]

The decision rule under the critical value method would be to reject the Null Hypothesis when the value of the test statistic is in the rejection region. In other words, reject \(H_o\) when \(Z >1.96\) or \(Z<‐1.96\).

Based on this result, the decision is fail to reject \(H_o\) , since the test statistic does not fall in the rejection region.

Alternatively (and preferably) the statistician could use the p‐value method of decision rule. The \(p\)‐value for a two‐tailed test must include all values (positive and negative) more extreme than the Test Statistic, so in this example we find the probability that \(Z < ‐1.44\) or \(Z > 1.44\) (the area shaded blue).

Using a calculator, computer software or a Standard Normal table, the \(p\)‐value=0.1498 . Since the \(p\)‐value is greater than \(\alpha\) the decision again is fail to reject \(H_o\) .

Finally the statistician must report the conclusions and make a recommendation to the company’s management:

“There is insufficient evidence to conclude that the machine that fills 16 ounce soy sauce bottles is operating improperly. This conclusion is based on 36 measurements taken during a single hour’s production run. I recommend continued monitoring of the machine during different employee shifts to account for the possibility of potential human error”.

The statistician makes the weak statement and is not stating that the machine is running properly, only that there is not enough evidence to state that the machine is running improperly. The statistician also reports concerns about the sampling of only one shift of employees (restricting the inference to the sampled population) and recommends repeating the experiment over several shifts.