Research Final Exam Flashcards

1
Q

what is a case study?

A

detailed report of an individual case

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2
Q

an effective case study can contribute to existing knowledge by? (3)

A

expanding knowledge of an interesting case, thereby

  1. informing clinical decision making
  2. challenging/supporting theoretical formulations
  3. providing groundwork for future investigations
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3
Q

limitations of a case study

A
  1. doesn’t have controls (so can’t determine cause-effect)
  2. cant generalize
  3. no definitive proof
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4
Q

know the 5 key elements of an effective case study

A

see NB paper

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5
Q

What are two ways for getting equivalent groups in group experimental designs? Explain them

A
  1. Randomization: randomly assign people to groups, works well for large numbers
  2. Matching:
    - overall: overall, groups have same mean age, similar numbers of boys/girls, etc.
    - matched pairs (every person in exp, group has a one to one match with someone in control group)
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6
Q

with group experimental studies, there are usually how many in a group?

A

8-10 or MORE

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7
Q

it’s important to know what _____ groups were formed on. Explain.

A

subject characteristics

- is there anything important they didn’t tell you about?

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8
Q
  • in single subject designs, what tells us about significance of results?
  • in group designs?
A
  • line graphs typically

- STATS

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9
Q

what’s the most common type of experimental design?

A

pretest-posttest experimental design

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10
Q

with pretest-posttest experimental design, what should the groups look like before and after therapy?

A
  • EQUAL before

- DIFFERENT after

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11
Q

what’s a weak experimental design?

A

posttest only group design

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12
Q

example of factorial design?

A

did mild, moderate, or severe kids benefit most from the treatment?

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13
Q

Another name for IV is what?

A

factor

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14
Q

what if you have a group that gets treatment that you do a pre and post test with, but no control group?

A

CASE STUDY

- no controls to establish cause-effect

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15
Q

how many subjects in single subject typically?

A

1-5

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16
Q

Name and explain 4 control mechanisms in single subject design

A
  1. Baselines: multiple measures of DV prior to treatment, shows that DV isn’t changing before treatment.
  2. Replication: intrasubject & intersubject
  3. Withdrawal/Reinstatement: take therapy away then reinstate to show cause-effect
  4. Rapid alterations: controls for extraneous variable of time
17
Q

If you want to compare 2 treatments with withdrawal, what do you need to do?

A
  • need withdrawal period between treatment
18
Q

with withdrawal, want to pick a behavior with a __ percent accuracy initially. Why?

A

LOW

- don’t want them to master it, so you can show cause-effect

19
Q

what’s a weak withdrawal design with multiple treatments? What’s a stronger design and why?

A
  • ABC

- ABAC: there’s withdrawal between, not one after another

20
Q

If there’s more than one subject with withdrawal and more than one treatment, you’d want to do what?

A

alternate the order in which they’re getting the treatments

21
Q

See example graphs in single subject PP

A

study

22
Q

can you compare 2 different treatments with multiple baseline?

A

NO

23
Q

what’s a multiple probe design?

A

same as multiple baseline, but decreases the frequency of data collection (periodically record data)

24
Q

when can you see INTRASUBJECT replication

A

multiple baselines across behaviors, withdrawal designs, rapid alternating

25
Q

methods of single subject should include what about subjects? ex

A

A LOT about each

- age, disorder, test results to describe impairment/strengths/weaknesses, past treatment

26
Q

in SS design, need detailed description of what else?

A

IV: time, materials, cueing

27
Q

most common way to depict data with SS? sometimes?

A

LINE GRAPHS depicting daily data

  • bar chart: means per condition if comparing 2 treatments in rapid alternating or withdrawal desing
  • gain in each behavior if multiple baseline