Experimental Research Designs Flashcards

1
Q

What are experimental designs?

A

Experimental designs entail the manipulation of a variable (IV) to test the effects of the manipulation on some outcome (DV).

Needs to have manipulation.

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2
Q

What is causal research?

A

Causal research can be defined as a research method that is used to determine the cause and effect relationship between two variables.

Conclusive research.

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3
Q

What are the two objectives of causal research?

A

1) Isolate etiological causes of HB and disease outcomes

2) Determine whether interventions are effective in achieving intended outcomes

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4
Q

What are the three necessary conditions for causation?

Describe them.

A

1) Relationship condition
Variable A and variable B must be related.

2) Temporal antecedence condition
Proper time order must be established

3) Lack of alternative explanation condition
Relationship between A and B must not be due to third confounding variable

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5
Q

What are defining characteristics of experimental research design?

A

Manipulation of IV and control over extraneous variables.

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6
Q

What is the IV?

A

The variables chosen by the INVESTIGATOR to determine its effect on the DV.

Is MANIPULATED by the investigator.

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7
Q

What is the DV??

A

The variable(s) that is being tested.

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8
Q

What are extraneous variables?

A

Not directly related to the hypothesis being tested but may have an effect on DV.

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9
Q

How do extraneous variable threaten internal validity?

A

Extraneous variables may provide alternative explanations or rival hypotheses that threaten internal validity.

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10
Q

What is internal validity?

A

The extent to which our study allows us to answer the question we want to answer

Extent to which study establishes cause and effect RL between IV and RV

Ability of a design to test hypothesis it was intended to test.

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11
Q

What is external validity?

A

The extent to which findings of the research study can be generalized to the population under study.

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12
Q

What is efficaciousness versus effectiveness?

A

Efficacy:
Having an effect.
Performance of an intervention under ideal conditions.

Effective:
How well it performs in real world.

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13
Q

What is a one-factor versus two-factor design?

A

One factor has only one thing being treated (no control).

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14
Q

What are the 9 threats to internal validity?

A
Hawthorne effect
Diffusion
History
Maturation
Testing
Instrumentation
Statistical regression 
Differential selection
Differential attrition
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15
Q

What is the Hawthorne effect?

A

The alteration of BH by subjects of a study due to their awareness of being observed (need to have control group to avoid this).

Threat in one-group and two-group without placebo.

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16
Q

What is diffusion?

A

Distinction between intervention and control group are not as separate as they should be (results might be due to contamination of control group); maybe people from same household cannot be in the same study - can try to control with study design.

Threat to two-group or multi-group design.

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17
Q

What is history threat?

A

Any event that might have occurred between observations outside of trial.

Threat to one-group design.

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18
Q

What is maturation threat?

A

Results might be due to PPTs growing older, wiser, stronger, etc. between observations.

If history and maturation are threats, include control group.

Threat to one-group design.

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19
Q

What is testing threat?

A

The results are due to the number of times responses were measured (PPTs have answered questions before that might effect how they will answer questions in the future)- people might just get better with a test.

Control group needed as you would expect testing effect for both groups so any differences between the groups would be due to other reasons.

One group threat.

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20
Q

What is instrumentation threat?

A

Results might be due to a change in the measuring of instrument between observation.

One group threat.

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21
Q

What is statistical regression threat?

A

Regression to the mean, results might be due to the selection of PPTs based on extreme scores, and when measured again, scores might move back to an average level.

One group threat.

22
Q

What is differential selection threat?

A

Results might be due to differences that existed between PPTs in groups before the treatment occurred); with random assignment hope that people in two groups are similar to each other as much as possible (large sample this is less likely to be threat as more likely to equalize out).

Two group or multi-group threat.

23
Q

What is differential attrition/mortality?

A

Results might be due to the systematic differential loss of PPTs from each group; intensive intervention group is more likely to stay in the study (lose more people in control group).

Two or multi-group threat.

24
Q

What is error variance?

A

Variability in the DV that cannot be attributed to IV and instead to extraneous variables.

Measurement error or residual error. Random stuff that affects our measurements.

Time of day, noise in BG, etc.

25
Q

What is sampling bias?

A

Occurs when sample is not representative of the population.

26
Q

What is random assignment?

A

A method that uses chance to assign participants into two or more respective groups.

27
Q

What are the types of TRUE experimental designs?

A

Posttest control group design.

Pretest posttest control group design.

Matched-pairs group design.

28
Q

What is a posttest control group design?

A

Between-subjects design.

Two groups that are randomly assigned are compared on levels of DV following manipulation of IV.

Post-tests are givens to determine if a difference between groups exists.

29
Q

What are strengths of posttest control group design?

A

Quick and inexpensive.

Random.

30
Q

What are weaknesses of posttest control group?

A

No pretest so no baseline per person and no knowledge of past differences between groups.

31
Q

What is a pretest posttest control group design?

A

Includes pretest to assess differences between groups.

Between subjects design.

Random assignment. Two groups are compared on levels of DV after manipulation of IV.

Can be considered RCT.

32
Q

What is a matched-pairs group design?

A

Between-subjects design with randomization.

Subjects matched by characteristics to form pairs. One is placed in control and the other in intervention.

Used when characteristic is strongly associated with DV and may not get equally distributed across groups randomly.

33
Q

What are strengths of matched-pairs group design?

A

Significant reduction in potential confounding effect of matched characteristic.

Allows for control of differential selection on characteristic that would otherwise affect dependent variable.

34
Q

What is weakness of matched-pairs group design?

A

Time-consuming.

Not possible to truly match all PPTs in one group with a pair in the other.

35
Q

What is a within-subjects or repeated measures design?

A

Subjects serve as their own controls are are exposed to all levels of IV.

36
Q

What are some quasi-experimental designs?

A

Within-subjects or repeated measures design NEED TO CHECK.

Non-equivalent control group design.

Interrupted time series design.

37
Q

What is a quasi-experimental design?

A

Manipulation of IV but no randomization.

38
Q

What are strengths of within-subjects design?

A

Reduces error variance

39
Q

What are weaknesses of within-subjects design?

A

Carryover effects such as:

Learning, fatigue, habituation, sensitization

40
Q

What is a cross-over trial?

A

Specific form of within-subjects design with randomization.

41
Q

What is the benefit of a cross-over trial?

A

Reduces carryover effects.

42
Q

When is a crossover trial appropriate?

A

When IV effects are short and reversible.

We know effects are not due to passage of time, learning, or other effects.

43
Q

What is a smart design?

A

A study design that has to do with optimization of treatments.

Multiple points of randomization.

Can see effects of randomization and see when and for whom interventions are appropriate.

44
Q

What is random assignment?

A

Units are assigned to conditions purely by chance and each unit has a nonzero probability of being assigned to a particular condition.

45
Q

What is random sampling?

A

Random selection of study subjects from a population so estimates derived from sample can be taken as an approximation of estimates in the population.

46
Q

What is a randomized experiment?

A

Also known as a true experiment, a randomized experiment whereby the study design entails randomly assigning study subjects to groups.

47
Q

Describe simple randomization.

A

Units assigned to conditions by chance.

48
Q

Describe block randomization?

A

Main point is to balance number of PPTs in each treatment group.

Select size of block.
Assign PPTs in that order.
Repeat.

49
Q

Describe stratified randomization.

A

Used to achieve balance in groups based on covariates of interest.

Separate blocks for each combination of covariates generate and subjects assigned to the appropriate block.

Divide into subgroups (strata) and perform separate randomization within each.

Need to know participants’ characteristics for strata before randomization.

50
Q

Describe covariate adaptive randomization.

A

Seeks to ensure balance throughout study.

Minimize PX differences in characteristics across treatment groups.

Often done through minimization.

A new participant is sequentially assigned to a particular treatment group by taking into account the specific covariates and previous assignments of participants.

51
Q

Describe a non-equivalent control group design.

A

A group is matched as closely as possible to the experimental group and used as a comparison group.

52
Q

Describe an interrupted time series design.

A

Strongest quasi-experimental approach for evaluating longitudinal effects of interventions.

Collect data at multiple instances over time before and after treatment.

Key time point: when intervention delivered.

Treatment effect is demonstrated if the pattern of post-treatment responses differs significantly form the pattern of pretreatment responses (e.g., change in level or slope).