Lecture 3: T-test, one way ANCOVA and mixed ANOVA Flashcards

• Understanding that differences between groups can be tested with both regression analysis and ANOVA. • Understanding in which cases controlling for a covariate (ANCOVA) is the appropriate method. • Understanding in which cases a mixed ANOVA is the appropriate method and which follow-up analyses are required. • Being able to perform the above methods in SPSS, interpret its results, and to report them.

1
Q

When is a t-test used vs an ANOVA?

A

Both need a continuous dependent variable, but ANOVA needs more than 2 groups while t-test has a max of 2 groups.

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2
Q

What is null and alternative hypothesis for a t-test?

A

H0= 2 means are equal
H1= 2 means are not equal

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3
Q

What is null and alternative hypothesis for an ANOVA?

A

H0= 2 or more means are equal
H1= 2 or more means are not equal

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4
Q

What are the characteristics of non-specific hypotheses?

A
  • post hot tests used-> all possible comparisons
  • correct for familywise error rate
  • but has less power than planned contrasts
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5
Q

What are the characteristics of specific hypotheses?

A
  • planned contrasts used
  • simple effects analyses can be used as a follow-up analysis
  • not all possible comparisons and looks at just the ones you have a hypothesis about
  • more power
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6
Q

How is elimination of confounds a reason for carrying out an ANCOVA?

A

Can correct for initial differences despite random assignment resulting in a more accurate comparison. It can thus filter out explained variance, so the unexplained variance in wellbeing is smaller. The uniquely explained variance is also smaller. The ratio of uniquely explained variance to unexplained variance changes, so the F value can be smaller or greater depending on the data

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7
Q

What are the steps of an ANCOVA?

A
  1. check assumption so whether the regression lines are parallel (no significant interaction effect between covariate and intervention)
  2. If the assumption is met then do the actual ANCOVA without the interaction term-> just report the F values for the intervention
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8
Q

When do we correct for initial group differences on the covariate?

A

Only in randomized groups that come from the same population

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9
Q

What is the other reason for carrying out an ANCOVA?

A

To reduce variance within groups which allows for a more sensitive comparison. The unexplained variance in wellbeing is smaller, so the effect of the intervention is determined more sensitively, So the intervention explains relatively more variance in the outcome. F value is greater and more easily significant then.

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10
Q

Why would you do a mixed ANOVA?

A

If you want to use several assessments, as one-way ANOVA tests for differences at one-time. So then you can compare changes over time between groups

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11
Q

What are the assumptions of a mixed ANOVA?

A
  • Dependent variable continuous (assumption 1)
  • (Co)variances in all groups equal (assumption 2)
  • Data of subjects are independent (assumption 3)
  • Dependent variable is normally distributed in each group
    (assumption 4)
  • Sphericity (more than 2 repeated measurements)
    (assumption 5)
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12
Q

What is reported for a mixed ANOVA?

A

Any significant main effects, interaction effect all found between within-subject effects

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13
Q

What is the homogeneity of regression slopes?

A

The relationship between covariate and dependent variable should be similar in all groups. If the assumption is not met, then the F-distribution is actually a different distribution, the type I error is inflated, and the power is suboptimal

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14
Q

How can covariate results be reported?

A
  • “The covariate, love of puppies, was significantly related to the participant’s happiness, F(1, 26) = 4.96, p = 0.035, r = 0.40. There was also a significant effect of puppy therapy on levels of happiness after controlling for the effect of love of puppies, F(2, 26) = 4.14, p = 0.027”
  • For contrasts: “Planned contrasts revealed that having 30 minutes of puppy therapy significantly increased happiness compared to having a control, t(26) = -2.77, p = 0.01, r = 0.48, but not compared to having 15 minutes, t(26) = -0.54, p = 0.59, r = 0.11.”
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15
Q

How to check whether the covariate is the same across groups?

A

using a one-way ANOVA which should not be significant

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16
Q

Why should the covariate be independent of the treatment effect?

A

→ dependence occurs most often if no random assignment used
→ shared variance of treatment and covariate cannot be separated, one cannot control for a covariate
→ random assignment and matching based on covariate could both eliminate the problem
→ if there is temporal additivity (different treatment groups would have changed to the same degree without intervention), then treatment groups may be biased if they are not equal on the covariate

17
Q

How to report all results for a covariate?

A

There was a significant main effect of group, F(1, 57) = 26.71, p < .001. Insomnia symptoms were, across both measurements, on average lower for online CBT-I than
for WLC. There was also a significant main effect for measurement, F(1, 57) = 208.00, p < .001. Insomnia symptoms were, across both groups, on average lower at
posttest than at pretest. Finally, there was a significant interaction effect between measurement and group, F(1, 57) = 71.22, p < .001. The effect of measurement differed between groups, with the decrease in insomnia symptoms from pre- to posttest being greater for the online CBT-I group than for the WLC group.

18
Q

Why could it be important to include depressive symptoms at pre-test as a covariate in the analysis of the effect of group on insomnia symptoms at post-test?

A

Because you want to rule out that differences found between groups in insomnia symptoms (ISI) at posttest are due to initial (pretest) group differences in depressive
symptoms (CES-D). You are interested if there is an effect of online CBT-I compared to WLC on insomnia symptoms at
posttest in subjects who are comparable in terms of depressive symptoms (CES-D) at pretest.