Week 5 revision Flashcards

1
Q

Define Type 1 error

A

Incorrectly accepting a hypothesis when there is none - false positive.

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2
Q

Define Type 2 error

A

Accepting a false null hypothesis when there is an effect - false negative.

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3
Q

Define power in technical and useful terms

A

The probability of correctly rejecting a false null hypothesis.
The degree to which we can detect treatment effects when they exist in the population.

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4
Q

What are the 3 situations in which you might care about power?

A

When designing a study.
Finished a study without a significant effect.
Finished a study with a significant effect.

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5
Q

What are the 4 factors that affect power, and what these factors’ effects are (What conditions increase statistical power)

A

Sample size increase statistical power.
Alpha level, larger increases, smaller decreases
Larger effects increase statistical power.
Error variance reduction increases power.

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6
Q

Explain what a power estimate means (e.g., power = .41), and what the threshold is
for optimal levels of power.

A

Threshold = .1/.05
Power estimate is the estimated amount of participants needed to find a statistically significant effect in a study

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7
Q

Identify the pieces of information you need to calculate power estimates, in a priori
analyses (2) and post hoc analyses (3).

A

A prior = estimates of effects size, estimates of error (MSerror)
Post Hoc = effect size, MSerror, N in your study.

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8
Q

Explain the three caveats (i.e., cautionary tales/qualifications) of power analyses.

A

Increasing a reduces T2E but increases T1E
Reducing a reduces T1E but increases T2E
An interaction means effects are qualified by a control variable (creates confound)

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9
Q

Identify the strategies you can use to maximize power.

A

Sample size = increase sample size
Alpha level = increase alpha levels
Larger effects = focus on larger effects
Error variance = reduce error variance

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10
Q

What are the strategies you can use to reduce error variance? (4)

A
  1. Improve operationalization/validity of
  2. variables
    3.Improve measurements/internal reliability of variables
  3. Improve design (e.g. by blocking)
    Improve method of analysis (e.g. blocking or ANCOVA)
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11
Q

What is a control/concomitant variable?

A

An additional factor which are well known/less novel/less interesting that can explain common variance in the DV.

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12
Q

Explain how to use blocking in between-participants designs. (3)

A
  1. Pre-measure control variable.
  2. divide into groups according to results.
  3. stratify random assignment to IV levels.
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13
Q

Explain how blocking differs from experimental designs.

A

Experimental designs = fully randomized
Blocking = stratified random assignment

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14
Q

Explain how the blocking variable fits in with the predictions made in a research study and the reporting of findings.

A

Blocking results aren’t usually of interest, but are still reported in case of any interactions.

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15
Q

What are the two applications of blocking?

A

Increases power by reducing error variance. e.g. caffeine vs Problem solving (IQ)
Detecting potential confounds that explain the systematic variation in results. e.g. experimenter effects.

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16
Q

What happens if the blocking variable does not reduce error variance?

A

Then it is unrelated to focal IV and unnecessarily decreases the df(error)

17
Q

How does blocking reduce error variance?

A

Reduces error by blocking any attributable error variance into another variable.

18
Q

What is the difference between an independent variable (IV), a control variable, and a confound variable?

A

IV = the focal factor of a study (Predicted systematic variance)
Control V. = A variable introduced to help block variance (reduced error).
Confound V. = An unwanted significant effect ( additional systematic variance)

19
Q

Explain how blocking can help you detect potential confounds.

A

If an interaction is found, it means that the blocking/control variable is effecting the generalizable of the treatment IV and qualifies it’s effects.

20
Q

What are the advantages of blocking?

A

-Can make treatment groups more equal in variance then if randomly assigned.
-Greater power because of reduced error.
-Can check for interactions or generalizability of treatments.

21
Q

What are the disadvantages of blocking?

A

-Costs more
-Lose power if blocking is poorly correlated to variable because it will result in a smaller df(error) meaning more likely to make T2E
-Could lose information if blocking is treated as having discrete levels when it is continuous.