Slides 5 Flashcards

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1
Q

what is the gold standard in psychology experimental designs

A

random selection

  • every individual I that population has the same chance to be selected to participate in that research study
  • improves external validity
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2
Q

why isn’t true random selection performed often if its the gold standard?

A

rarely feasible unless the population is very narrowly defined

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3
Q

when using convenience samples, what should the investigator do?

A

the investigator should evaluate and at least discuss whether unique features of the sample contributed to the results

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4
Q

what is equivalence of groups in a study dependant on? why?

A

N

  • even if participants are randomly assigned groups, if your sample is very small, say 10, it could be that by chance one group is different than the other
  • also: in small groups, there isn’t enough power there to determine if your groups are significantly different, so really, you’re in the dark
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5
Q

what to do to make sure groups are equivalent if sample of participants for study is small

A

match participants

  • guarantees equivalence on key variables
  • of course have to be cautious with this bc sometimes you may think you’re matching participants when in fact you aren’t
    ex: multiple ways to get same IQ score
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6
Q

If the midterm includes an experimental design that says its nonrandom, what is it likely to be ?

A

quasi-experimental design

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7
Q

what does R mean in experimental design notation

A

random assignment

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8
Q

what does O mean in experimental design notation

A

observation/assessment

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9
Q

what does X mean in experimental design notation

A

treatment or manioulation

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10
Q

what is this design called

R O1 X O2
R O3 O4

What are it’s strengths? Weaknesses?

A

Pretest-posttest control group design

Strengths:
is period between pretest and posttest are equivalent than many threats to interval validity are controlled for

  • allows for matching using pretest scores
  • increased power, better examination across groups
  • allows for predictors and descriptors of attrition

Weaknesses:
pretest sensitization
- did exposure to the pretest contribute to the response of the manipulation?

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11
Q

what is this design called

R X O1
R O2

What are it’s strengths? Weaknesses?

A

posttest only control group design

strengths:
pretest sensitization
- did exposure to the pretest contribute to the response of the manipulation?

weaknesses
is period between pretest and posttest are equivalent than many threats to interval validity are controlled for

  • allows for matching using pretest scores
  • increased power, better examination across groups
  • allows for predictors and descriptors of attrition
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12
Q

what is this design called

R O1 X O2
R O3 O4
R X O5
R O6

what does it do?

A

Soloman Four-group design

evaluates the effect of the pretest

  • typically only really used when we are sure that pretesting will produce problems
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13
Q

what is a factorial design

A

allows for simultaneous investigation of the effect of two or more variables

allows for testing of interactions

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14
Q

what is this design called

nonR O1 X O2
nonR O3 X O4

what does it do?

A

Quasi-experimental design

  • includes pretest, posttest, and other variations
  • doesn’t have random assignment
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15
Q

Why might an experiment have nonrandomly assigned subjects

A

subjects who are already in separate clinics, schools, or classrooms
- there is a reason they cannot be compared

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16
Q

what is this design called

R O1 XA O2 XB O3
R O4 XB O5 XA O6

what does it do?

A

crossover design

  • subjects differ only in the order they receive tx
  • design is optimal for 2 randomly assigned groups
17
Q

what happens for multiple treatments counterbalanced designs

A

in crossover deisgns, the order of treatments are counterbalanced

increased number of treatments becomes more difficult

18
Q

what is it called when an experimental design has sequences arranged where each treatment occurs in a positive only once (kind of like suduko)

A

a latin square

A B C D
B A D C
C D A B
D C B A

19
Q

what is not good about latin quare designs

A

not every treatment is proceeded and followed by every other treatmet so its possible there is an interaction between a treatments affectiveness and its order to other treatments

20
Q

What happens in a true counterbalanced design

A

there is random assignment to every possible sequence of treatments

21
Q

what are sequence effects

A

arrangement of treatments contributes to effects - like carry over effects

22
Q

what does a no treatment control group accomplish

A

helps rule of confounds

-

23
Q

how do you assign your no treatment control groups

A

randomly assign potential subjects

- cannot use drop outs as controls (they are self selected as opposed to randomly selected

24
Q

what often happens with no treatment control groups

A

may seek treatment elsewhere

they often drop out

25
Q

what are waitlist control groups

A

use subjects who are waiting for treatment as a control group

treatment is given after treatment is over for group 1
- must only use participants who in advance agree to remain if placed in this group, otherwise could introduce serious confounds

waitlist group completes 2 rounds of pre-assessment and one of post

26
Q

what are no contact control groups

A

they don’t even know they are in the study

  • pre-test info from another sutyd or a large screening
  • ethical issues
  • subsequent test info obtained through a ruse so they don’t know its related to the study
27
Q

what are nonspecific-treatment or “attention-placebo” control groups

A

nonspecific factors are controlled so the specific mechanisms of change can be somewhat isolated and evaluated

  • control for common factors
  • many ethical issues
  • reduced faith in therapy
  • leads individuals to never seek real treatment
  • problem with withholding treatment
28
Q

what are routine/standard treatment control groups

A

all receive an acceptable treatment

limited attrition
controls for nonspecific factors
more likely to have therapist compliance

29
Q

what are yoked control control groups

A

control subjects are matched with subjects to complete aspects of the protocol
- issues with construct validity should drive this decision (rule out demand characteristics)