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Lecture 10
Within-Subjects Analysis of Variance

When to Use Within-Subjects ANOVA
The within-subjects ANOVA is really just an extension of the paired t-test discussed earlier. It is used whenever there are repeated measures or repeated treatments of an individual, paired participants (e.g., triplets), or matched participants (e.g., four participants are yoked according to the amount of daily exercise they get). Daniel describes two forms of the within-subjects design, the design he calls the "randomized complete block design" and repeated measures. The randomized complete block design is a study in several participants are matched or yoked together (e.g., on age), then one member of each grouping is randomly assigned to each of the treatment conditions. If there are three treatment conditions (e.g., three different drugs are given), each person in a group of three would be sent to a different condition. But in order for it to be valid to use a within-subjects analysis, the groupings of participants has to be done on some basis. For instance, triplets or three people matched because they have the same number of years experience on the job. Repeated measures, on the other hand, indicates that each person is measured several times. In general, the within-subjects ANOVA applies to matching, repeated measures, repeated treatments, or any time participants are yoked together.

An example of a within-subjects design would be a hypothetical study on cholesterol which has four treatments: high oat fiber diet, exercise, a low fat diet, and low calorie diet. In a between-subjects version of the study, different participants would be in each of these four conditions. In a within-subjects version of this study, each participant might be exposed to each of these treatments for a period of time. So, if I was in the within-subjects cholesterol study (or, to be more specific, we would call this a repeated measures design), I would spend a month eating oatmeal for breakfast. Then, the next month, I would stop eating oatmeal, and begin an exercise regimen. The following month, I would stop exercising, and start reducing fat intake. And so on.

One can think of the scores on the cholesterol measure as blocked together according to each individual. Each person has four scores. At the end of each month (and, hence, each treatment) a cholesterol count is taken. In a way, each participant has a block of four scores--so you can see the similarity to the randomized block design.

Like the between-subjects ANOVA and the between-subjects t-test, the within-subjects ANOVA and the within-subjects t-test are related. The within-subjects ANOVA can be used for two or more groups, and when used with two groups the t-test and the F-test will lead to the same conclusion ( and ).

The same benefits of the within-subjects t-test over the between-subjects t-test still apply. We need fewer participants overall and we have more power, because each individual (or block) acts as its own control.

The Analysis
The analysis approach is similar to that of the paired (or within-subjects or matched) t-test. We are intrested in the differences between scores for an individual (remember when we calculated the difference score, d, for each individual?). We will also use a similar ANOVA logic to the logic we used with the between-subjects ANOVA. We will calculate the variation of the scores for an individual relative to the mean of scores for that individual. In other words, we want to know how much each participant's scores change from treatment to treatment. If one or more of our cholesterol treatments had an effect, we would expect cholesterol counts to change fairly dramatically from month-to-month.

A Note on Notation
The notation for this analysis does not change dramatically, but we need to extend it a little. Previously, we used a dot to indicate that we had combined scores across individuals. For example referred to the sum of individual scores in a group. This time we will do some adding the other way, so that we combine scores across treatments rather than individuals. So, the sum of scores for one participant in the study, summed across treatments is symbolized by The sum of cholesterol counts for the second participants who has completed all four treatment conditions would be symbolized as Thus, stands for the sum of individuals for the second treatment, and stands for the some of treatments for participant 2. Similary, represents the mean cholesterol score for participant 2 across all treatments, and represents the mean of all participants for treatment number 2.

Example

Participant #

Oat Fiber

Exercise

Low Fat

Low Calorie

1

180

200

160

200

740

185

2

230

250

200

220

900

225

3

280

310

260

270

1120

280

4

180

200

160

200

740

185

5

190

210

170

210

780

195

6

140

160

120

110

530

132.5

7

270

300

250

260

1080

270

8

110

130

100

100

440

110

9

190

210

170

210

780

195

10

230

250

200

220

900

225

2000

2220

1790

2000

 

 

200

222

179

200

 

 

Now we have several sums of squares to compute.

 

Formula

Name

Description

Example

Sum of Squares Treatment

Represents variation due to treatment effect

Sum of Squares Block

Represents variation within an individual (within block)

Sum of Squares Error

Represents error variation

Sum of Squares Total

Represents total variation

 

Now for the mean squares and the computed F-value:

SSTr=924.75

k - 1=4 - 1=3

SSBl=25705.63

n - 1=10 - 1=9

not needed

 

SSE=88067.12

(n - 1)(k - 1)

=(10 - 1)(4 - 1)=27

 

SST=114.697.50

kn - 1 = 40 - 1 = 39

 

 

Interpretation
To check whether the calculated F-value of 31.75 is significant, we compare that value to the critical value of obtained from Table G, using the table labeled .95 (for a=.05) and 3 and 27 d.f. Our test is significant, indicating that there were differences in cholesterol treatments that are unlikely to be due to chance. What if we had set alpha to a lower value, say .01, would the test still be significant? To see, look up the same d.f. values in the .99 (a = .01) table. If our calculated value exceeds that table value, we would have significance at p <.01. Often authors report the lowest p-value at which they would find significance (e.g., p < .05, p < .01, p < .001), given their calculated value. Computers print out the exact p-value, so all one really has to do is look to see if the p-value printed out is less than .05, .01, or .001.

 

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