Experimental Designs Flashcards

1
Q

Factorial designs

A
  • when more than one independent variable is used
  • 3 main types:
    • between subject
    • within subject
    • combination of within and between:
      1. Mixed
      2. Nested
  • each variable or factor has 2 or more levels
  • use ANOVAs to analyze
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2
Q

Between subject designs

A

2 types:

  1. completely randomized
  2. Matched group designs (must ensure groups are equal so match one participant from one group with one from other group to ensure equal STD)
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3
Q

Within subject designs

A
  • also called repeated measures designs or randomized-blocks designs
  • 3 main types:
    1. same subject observed under all treatment conditions
    2. same subject observed before and after a treatment (pre+post test design)
    3. subjects are matched on a subject variable (organismic variable or individual difference variable) and then randomly assigned to the treatments
      • is actually a between subject design requiring a within subject ANOVA
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4
Q

Within subject design advantages

A
  • need less subjects
  • each level of the independent variable is applies to all subjects, so we can evaluate how each level of the independent variable affects each subject
  • each subject is its own control
  • excellent for assessing experiments on learning, transfer of training, practice effects
  • may help increase statistical sensitivity or power (subjects are not divided into groups, all subjects involved in all conditions)
  • small n research benefits from within designs
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5
Q

Within subject design disadvantages

A
  • practice effects: participants get better at it over time
    • (if not focus of study is a problem)
    • solution: appropriate counterbalancing procedures can counteract effects + make treatment order an independent variable (change it to see if it has practice effect)
  • differential carry over effects: lingering effect of one or more treatment condition (often an issue in drug studies)
    • solution: recovery periods
    • anti-depressants good example because some have long lasting effects
  • violation of statistical assumptions: not enough people etc
    • solution: use more strict significance level
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6
Q

Carryover effects

A
  • fatigue: decreased performance with time
  • contrast: treatments are compared by subjects
  • habituation or sensitization: more exposure to stimulus causes increased or decreased sensitivity
  • adaption: tolerance (eg drug studies)
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7
Q

Nested designs

A
  • similar to mixed design but levels of factor A found under difference levels of a factor B ARE NOT THE SAME
  • usually because of a constraint
  • eg. Difference location

-groups would be: a1b1, a1b2, a1b3… a2b4, a2b5, a2b6

  • spatial: multiple samples of a single tissue type within a rat
    • estuaries are unique to each river
  • temporal: sub-samples in time can only be sampled at one time and not another

-more economical but some interactions cannot be evaluated

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8
Q

Interactions between variables

A
  • interconnectivity
  • variables: x, y, z
  • main effects: x, y, z
  • interactions: xy, xz, yz, xyz
  • you have an interaction when the effect of two or more variables is not additive
  • interactions make interpretation of experimental data more challenging
  • a significant interaction will often mask the significance of main effects
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9
Q

Additive interactions

A
  • effect of each independent variable/factor doesnt interact with the other
  • eg. Effect of phototherapy and melatonin on sleep quality. then the effects of PT doesnt impact melatonin, and melatonin doesnt impact effects of PT
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10
Q

Interactive interactions

A
  • when the effect of on factor plays a significant role on the effect of another factor
  • may look like the lines of two factors crossing/meeting
  • as one factor increases it may change how the other factor works or affects the dependent variable
  • if the results of one factor depend on another factor there IS an interaction
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11
Q

Ordinal interaction

A
  • on a graph there will be no overlap of the of the data

- eg. Lines of PT vs no PT with melatonin dont cross/overlap but there is still an interaction

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12
Q

Disordinal interaction

A
  • looking at a graph of both variables there will be an overlap in data
  • eg. Lines of PT vs no PT with melatonin dosage will cross over or overlap at at least one point
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13
Q

Antagonistic interactions

A
  • certain kinds of interactions can MASK the main effects of one or more variables
  • eg. (Graph with lines creating X shape) the independent variable melatonin is effective, but the statistical analysis fails to reveal statistically significant main effects for melatonin
  • analysis shows that there is no numerical difference in the averages, but the graph shows that the variables clearly have different effects
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14
Q

Having too many factors/levels

A
  • interactions will be harder to explain
  • more factors equals more possible interactions
  • need more power for more interactions
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