Validity of Experimental Design Flashcards

1
Q

What is validity?

A

The extent to which a concept, conclusion, or measurement is well-founded and corresponds accurately to the real world
The degree to which the tool measures what it claims to measure (validity of a measurement tool)
The degree to which the study establishes the relationship that is claims to establish (validity of a study)

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2
Q

What is experimental research?

A

The investigator manipulates conditions for the purpose of determining their effort on behavior
Example: randomized controlled trial

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3
Q

What is non-experimental research?

A

Non manipulative and observational
Examples: case studies, cohort studies, surveys, correlational studies

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4
Q

What are the three things that a true experiment requires?

A

Independent variable is manipulated by the researcher and dependent variable that is measured
Control group or comparison group
Subjects are assigned to groups using a randomization or pseudo-randomization process

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5
Q

What is the primary goal of research design?

A

To decrease or control the influence of attribute and extraneous variables as much as possible

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6
Q

What is an attribute variable?

A

Preexisting; level is inherent, not manipulated: physical, psychological or personal
Examples: Sex, race, age, educational attainment, hypertension

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7
Q

What are extraneous variables?

A

Factors not directly related to the purpose of the study, but that may affect the relationship between the variables that an experimenter is examining
Example: time of day they are seen

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8
Q

How do you control attribute/extraneous variables?

A

Homogeneity (use subjects that are homogeneous for the potential confounding variable; only recruit men or only in a certain age range)
Include in design (include the potential confounding variable in the study and analyze the results separately)
Matching (match subjects across groups in various levels of the independent variable on relevant characteristics)
Statistical control (perform analysis of covariance to determine if the presumed confounding variable had an effect on the outcome; if so, include the variables as a factor or covariate)
Repeated measures (if the variable changes over time or is context dependent)
Randomization (the best way to control; all possible confounding variables are distributed similarly across groups)

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9
Q

What is the analysis of covariance (ANCOVA)?

A

A statistical method that allows researchers to examine the effect of an independent variable on a dependent variable while controlling for the influence of a third variable (covariate)
It adjusts the dependent variable scores based on the covariate, providing a more accurate analysis by removing potential confounding variability in the outcome

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10
Q

What is random assignment?

A

Each subject has a known chance of being assigned to each group
Random assignment is used to equilibrate all potentially prognostic indicators across groups
Anything that might influence the outcome (confounder) is balanced across groups (ceteris paribus)

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11
Q

What is random selection?

A

Randomly choosing subjects from the accessible population
Rarely, if ever, accomplished

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12
Q

When should control groups be used?

A

To rule out the influence of extraneous effects
Compared to the experimental group
If the only difference between the experimental and control groups is the level of the IV, and if the treated group improves, but the control group does not, then we assume our manipulation caused the improvement (cause-and-effect)
In the best studies, the only difference between the experimental and control groups is the level of the IV

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13
Q

What is a single blind study?

A

Investigator or subject is blinded to group assignment

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14
Q

What is a double blind study?

A

Both subjects and researcher are blinded

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15
Q

What does blinding do for the study?

A

Blinding protects from subject and researcher bias by disguising group assignment and hypothesis
Blinding is more important when the outcome measured is subjective (you don’t have to blind if the outcome is death)

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16
Q

What is statistical validity?

A

There is a relationship between the independent variable and the dependent variable
Concerns the potentially inappropriate use of statistical procedures for analyzing data
Leads to invalid conclusions about the relationship between the IV and DV

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17
Q

What is power?

A

The probability of finding a statistically significant difference if a real difference exists
Conventionally it is set at 80%

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18
Q

What does power depend on?

A

Sample size (all else being equal, a larger sample means more power)
Variability (the greater the heterogeneity, the more difficult it is to find a difference)
Effect size (how large is the difference)

19
Q

What are the types of error?

A

Type I - reject the null hypothesis when a true difference does not exist (false positive)
Type II - failure to reject the null when really, a significant difference does exist (false negative)

20
Q

Do small samples yield low power and enhances the probability of error II?

21
Q

What is internal validity?

A

Evidence that the independent variable causes the dependent variable
Ruling out alternative explanations for observed changes attributable to the intervention
You must be able to establish that the IV (e.g., therapy) and only the IV caused a differential change in the DV across groups
True experiments have high internal validity due to the controlling properties of randomization and control groups

22
Q

What is external validity?

A

If the findings can reasonably be generalized beyond a specific experimental situation
The extent to which the results of a study can be generalized beyond the internal specifications of the study sample
Concerned with the usefulness of the results in the real (clinical) world

23
Q

Does clinical research lack complete control?

A

Yes
But it can closely replicate the clinical world
Absolute control is only possible in a test tube
If factors can’t be controlled and they may influence findings, they represent limitations to the study
Need to weigh the merits of control over internal and external validity (as one goes up the other goes down)

24
Q

What are the hallmarks of an experimental design?

A

Group assignment (preferably, random)
Concurrent control group

25
Q

What are the benefits of an experimental design?

A

Controls for bias; achieves equilibration
Optimized internal validity (did X cause Y?)

26
Q

What are quasi-experimental designs?

A

Studies that do not include a random group assignment and/or a control group

27
Q

Why are quasi-experimental designs used?

A

Often used in clinical studies because of practical and/or ethical limitations
Considered to be reasonable alternative to experimental designs and can offer important information

28
Q

What are some considerations about quasi-experimental designs?

A

Often involve non-equivalent groups that may differ at inception
Need to take potential alternative explanations into account when reviewing the findings
Require careful documentation of subject characteristics, a structured protocol, and blinding when appropriate

29
Q

What are the one-group quasi-experimental designs?

A

One-group pretest-posttest
One-way repeated measures
Time series

30
Q

What are the multi-group quasi-experimental designs?

A

Nonequivalent pretest-posttest
Nonequivalent posttest-only

31
Q

What is a one-group pretest-posttest?

A

One set of measurements taken before and after intervention on one group of subjects
Treatment effect = the difference in DV between pre-test and post-test
Independent variable = time
Two levels: pre-test and post-test

32
Q

What are some considerations for one-group pretest-posttest designs?

A

No comparison group means a threat to internal and external validity
Threats to internal validity: maturation and history effects

33
Q

When may a one-group pretest-posttest design be applicable?

A

The study is modeled after a previous study investigating a comparison group (eg, changes in DV in comparison group have been documented previously)
Extraneous (environmental) variables are minimized: eg, duration of time between pre-test and post-test measurements; isolation

34
Q

What are the threats to internal validity?

A

Maturation (aging in studies that occur over long periods of time; wounds heal naturally over time without intervention)
History (external events that could influence the results of a study)

35
Q

What is a one-way repeated measure design?

A

Focuses on how effects manifest over time within one group
Multiple measurements of the DV are taken post-test
Intervention can occur once or multiple times
Time is the IV

36
Q

What are some considerations for one-way repeated measures?

A

No comparison group means a threat to internal and external validity
History and maturation effects

37
Q

When is a one-way repeated measures design acceptable?

A

Acceptable when you want to account for trends

38
Q

What is a time series design?

A

Application of multiple measurements before and after treatment
Often used to assess/establish stability of observation

39
Q

What are some considerations for time series tests?

A

No comparison group = threat on internal and external validity
Potential maturation effects
Multiple measurements may produce a “testing” effect - performance may improve because of increasing familiarity and practice with the measurement

40
Q

What is a nonequivalent pretest-posttest design?

A

Similar to experimental design but random assignment to groups is not used
May be practical or ethical considerations to assignment
Can be used when groups are intact (classes, teams) or groups are self-selected (volunteered for new therapy)

41
Q

What are some considerations for nonequivalent pretest-posttest design?

A

With the inclusion of a pretest and comparison group, this design may be able to control for history, maturation, testing, and other threats to validity
Differential composition of groups (rather than intervention) contributes to differing outcomes (not randomized)

42
Q

What is a nonequivalent posttest-only design?

A

Existing groups who have and have not received intervention
No pre-treatment measure; typically retrospective
Worthless in terms of investigating cause-and-effect relations
Should only be used for exploratory purposes (eg, generating hypotheses for future study)

43
Q

What happens if you don’t blind?

A

Absent blinding of investigators and subjects, bias may have played a role in the study results