Module 8- Experimental Design Flashcards

1
Q

Purpose of the experimental design

A
  • make causal statements
  • only design where we can make causal statements about the IV and DV
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2
Q

Sound experimental design allows for

A
  1. determine the effect of the IV on the DV
  2. rule out alternative explanations; threats to internal validity
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3
Q

Single Group Design

A
  • involves one group of participants
  • measuring one level of the IV and DV
  • not a sound experimental design
    - does not make causal statements
    - does not rule out threats to internal validity ^ does not allow us to determine the effect of the IV on DV

group > treatment (IV) > Measurement (DV)

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4
Q

Comparison Group Design

A
  • involves a comparison group that does not receive the IV/ Treatment
  • helps us get an indication of the potential impact of the IV
    BUT not a sound experimental design bc does on rule alternative explanations/ threats to internal validity

Group A > Treatment (IV) > Measurement
Group B> No Treatment > Measurement

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5
Q

Random Assignment (R)

A
  • an aspect of a true experimental design
  • helps control threats to internal validity and confounding variables
  • how we assign participants to groups after they have been selected from the population
  • R is based on chance and no bias
  • all known and unknown confounds are randomly distributed therefore confounds do not affect the DV and not a threat to internal validity
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6
Q

Basic randomized control group design

A

R Group A> Treatment> Measurement
R Group B> NO treatment> Measurement

group B= control group (called a control group and not a comparison group bc we are “controlling” threats to internal validity)

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7
Q

Randomized pre-post control group design

A
  • includes a pretest measure of the DV

R Group A > Measurement> Treatment > Measurement
R Group B> Measurement> Treatment> Measurement

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8
Q

Advantages of randomized pre-post control group design

A
  • allows us to verify that the groups do not differ on the DV prior to the IV; want groups to be equal prior to IV
    - No initial differences on the DV
  • can give us a better understanding of the impact of the IV, by giving a baseline measurement of the DV
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9
Q

Disadvantages of randomized pre-post control group design

A
  • pretest can interact with the treatment (IV) to impact the DV
  • this can be a treatment to internal validity
  • when this occurs use to Solomon Four Group Design
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10
Q

Solomon Four Group Design

A
  • combines the 2 types of randomized control group designs ( basic and pre post)
  • one involves a pre test
  • one involves does not involve a pre test
  • allows us to assess if the pre test interacts with the treatment to impact the DV
  • assign participants to one of 4 groups

R Group A> Pre test> Treatment> Post Test
R Group B> Pre Test> No Treatment > Post Test
R Group C> Treatment> Post Test
R Group D> No Treatment> Post Test

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11
Q

3 criteria for a true experiment

A
  1. participants have to be randomly assigned
  2. at least 2 levels of the IV
  3. controls put in place for major threats to internal validity

all criteria must be met in order to be a true experiment and ^ make casual statements

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12
Q

Before the IV, F ratio should be

A

F=1
- bw group variance is equal to w/in group variance
- no systematic bw group differences ^ only accounting for chance/ error variance

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13
Q

If before the IV, F ratio is greater than one

A
  • a confound is likely contributing to systematic bw group variance
  • not good
  • we want groups to be equal before the introduction of the IV
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14
Q

2 main types of experimental designs

A
  1. b/w subjects design
  2. within subjects design
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15
Q

Between Subjects Design

A
  • participants have been randomly assigned to different groups and experience one study group/ level of the IV
  • DV measures are taken and compared bw groups
  • not experiencing all study groups/ levels of the IV
  • each group defined by the level of IV received
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16
Q

Simple random be subjects design

A

R Group A > Treatment> Measurement
R Group B> Treatment (no level of the IV)> Measurement

  • involves an experimental and control group
17
Q

Multi level bw subjects design

A

R Group A >Treatment Level 1>Measurement
R Group B >Treatment Level 2 >Measurement
R Group C >Treatment Level 3> Measurement
R Group D> Treatment Level 4 >Measurement

18
Q

why is bw subjects our go to design?

A
  • high internal validity
19
Q

What error is bw subjects prone to?

A
  • type 2 errors; fail to reject the null hyp, when the null hyp is false
  • bc gives a smaller F ratio than within subjects
  • larger sample can reduce type 2 errors
20
Q

Interpreting rejection of the null hypothesis

A
  • if have 2 groups, we can look at the data and see which group has the larger mean on the DV
  • BUT if have 3 or more groups, rejection of the null hypothesis tells us there is a difference somewhere, but doesnt say which groups differ
21
Q

Post Hoc

A
  • when have more than 2 groups
  • tells which means differ
  • done after the F test/ rejection of the null hypothesis
  • involves testing each pairing of means to determine where the difference lies
  • these keep type 1 errors controlled
22
Q

Priori Tests

A
  • comparing the means you expect to differ based on theory/hypothesis
  • rather than testing every pairing of means like in the Post Hoc tests
  • also done when have more than 2 groups
23
Q

when comparing more than one test group use

24
Q

when comparing more than one test group use

A

F test/ ANOVA

25
Q

Within Subjects Design

A
  • each participant experiences each level of the IV and provides a measure on the DV
  • no random assignment bc only one group of participants
  • same group of participants
26
Q

Advantages of Within Subject Designs

A
  • assures equivalence of groups bc it is the same group of people
  • what is does to the F ratio; minimizes the denominator therefore making a larger F
  • reduces the error term of the F ratio which increases the power and ability to detect the treatment effect
  • more sentive to effects of the IV; can pick up on small treatment effects
  • less prone to type 2 errors
  • dont need as many participants
27
Q

Order Effects

A
  • disadvantage to within subjects design
  • has to do with time; moving though sequential treatment conditions
  • experiencing multiple conditions can impact scores on the DV
28
Q

Practice and Fatigue effects

A
  • disadvantage to within subjects design
  • come about bc involved in numerous treatment levels
  • ex. participants become more comfortable with the math problems or bored ^ make more errors
29
Q

Carry over effects

A
  • disadvantage to within subjects design
  • due to the impact of one specific treatment condition
  • impact of the condition bleeds over into subsequent IVs
  • counterbalancing does not work bc order of treatment conditions does not matter
30
Q

Should not use within subjects design when

A
  • carry over effects are strong
  • bc can’t be controlled and major threat to internal validity
31
Q

Counterbalancing

A
  • helps to correct order effects
  • mixing up the order of treatment presentation so not all participants see the treatment in the same order
  • distributes order effects across all conditions
32
Q

Complete counterbalancing

A
  • includes all possible orderings of treatment conditions
  • each condition must be included equally as often and proceed each other a equal number of times
  • becomes hard when conditions grow; number of orderings grow exponentially as the number of conditions grow
  • effectively distributes order effects
33
Q

Incomplete counterbalancing

A
  • do when unrealistic to do complete counterbalancing
  • helps distributes order effects
  • every condition needs to be in the sequence but does not need to follow each condition equally
  • do when have a large number of condtions
34
Q

Latin Square

A
  • most common incomplete balancing procedure
  • number of presentations equals the number of conditions you have
  • all possible orders are not used