Specialized Designs Flashcards

1
Q

Quasi-experimental designs and ex post facto designs

A
  • used when something is missing…

- typically control groups and/or random assignment of subjects

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2
Q

Major categories of designs

A
  • pre-experimental: no control groups and no random assignment of subjects to conditions. Acceptable for pilot research only
  • experimental: controls groups, random assignment of subjects to conditions
  • quasi-experimental: often control groups, but no random assignment of subjects to conditions. Often take advantage of naturally occurring events- lack of control over variables
  • ex post facto: special case of between subject design. Here we extract a correlation between variables, not causation
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3
Q

Quasi-experimental designs

A
  • dont fill requirements for a true analytic experiment
  • issues with:
    • internal validity
    • external validity
    • random selection not possible or not respected
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4
Q

Quasi-experimental design examples

A
  • useful when statistical power is an issue
  • when few measurements are possible
  • when availability of participants is limited
  • random assignment of participants not possible
  • common mistake: pooling fallacy (compensating for lack of subjects by collecting more data
  • eg. Jet lag study issues:
    1. Finding participants involved in jet lag travelling willing to participant
    2. Variation in duration and distance of travel (#of time zones), departure and arrival times, direction of travel, sleep pattern/strategy before leaving for trip etc
  • solution: within-subject design (all participants go through all treatments
    • problems: order effects… solution: counterbalancing
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5
Q

Counterbalancing

A
  • when order effects may affect results
  • splitting groups so that half get one treatment first, and others get other treatment first to see if there is a difference in order
  • making order a factor
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6
Q

Ex post facto

A
  • researcher arrives after the fact. Nature has implemented treatment (groups are based on natural occurrences that make them distinct)
  • different environments (environmental or Contextual factors)
  • different dispositions (dispositional or individual factors
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7
Q

Prospective vs retrospective ex post facto

A
  • prospective: looking for effect of certain cause (i.e. have cause and look for the effect)
    • longitudinal study of individual to see effect
    • cohort designs
  • retrospective: have effect, but looking for the cause of it
    • investigate past of individuals who suffer given effect
    • case control designs or criterion group designs
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8
Q

Characteristics of EPF designs

A
  • participants selected after the fact for 2 reasons:
    1. Ethics (invasive studies)
    2. Subject variables (gender, age, education level, personality traits etc) become independent variables (treated as treatment condition)
  • rationale: cannot randomly assign people to different age groups etc
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9
Q

Prospective EPF internal validity issues

A
  • no random sampling from population
  • no random assignment conditions
  • confounded variables typical to the groups investigated (eg. High stress job participants smoke and drink more)
  • selection of subjects becomes complicated and strict criteria applied
  • convenience sample problematic (criteria themselves may be confounds)
    • eg. Air traffic controllers exposed to radiation from equipment
  • detection bias: common in biomedical research
    • probability that members of a certain group are diagnosed because of the nature of their job (i.e. air traffic controllers more likely to be medically assessed than a hobo)
  • accurate identification of members of respective groups based on criteria
    • eg. Finding people with GAD may be much easier than finding people with BPD
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10
Q

Prospective EPF external validity issues

A
  • choice of groups:
    • cant generalize from one group/occupation to another… ATC doesnt necessarily represent ALL high stress jobs for example
    • does the choice of group (eg high stress job) represent well with people with chronic stress (in general)
    • does occupational stress differ from domestic/personal stress?

-longitudinal nature of the study: issue of experimental mortality or attrition

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11
Q

Solutions for prospective EPF design external validity issues

A
  • matching: making sure that the groups do not differ on any other variable than ones selected
    • subject to subject matching of characteristics
    • distribution for distribution matching for descriptive statistics, mainly central tendency or variability
  • measure the variables: identify possible confounding variables and measure them to determine if they have effect or not
    • methods of analysis of covariance can help
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12
Q

Retrospective EPF designs

A
  • common in health research
  • similar problems as prospective designs
  • comparative advantages:
    • smaller number of subjects required
    • shorter time period
    • less money required
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13
Q

Specific issues with retrospective EPF designs

A
  • present context motivating the investigation
  • detection bias
    • historical issues in diagnosis and awareness
    • diagnosis likely made by different parties/doctors
    • differential assessment or perspective on stress between cancer group and healthy group
    • less extensive records in healthy group

Solutions

  • matching and measuring confounding variables
  • can be difficult because you must search back in time and you rely on memory of subjects and their families etc, which affect accuracy and completeness
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14
Q

Change

A
  • studying changes in time of structures and processes
  • ontogenetic changes: developmental research
    • changes in the individual neuron, brain, animal, person
  • historical change: cross-generational research
    • changes across generations (strains, families etc)
  • phylogenetic change: evolutionary research
    • changes in species and populations: speciation, natural selection
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15
Q

Developmental: longitudinal

A
  • example: social play development in children
  • longitudinal approach: same individual or group are tested, measured repeatedly over long period of time
  • disadvantages: test conditions become well known by children
    • are performance or behavioural changes due to experiment or maturation
    • long time period and money
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16
Q

Developmental: cross-sectional

A
  • example: social play development in children
  • approach: measuring different individuals at different ages and at the same time
  • disadvantage: individual differences can account for some effects and differences in development
  • solution: hybrid version (cohort sequential/ cross sequential
17
Q

Comparative/evolutionary

A
  • common in:
    • comparative and evolutionary neuroscience
    • comparative and evolutionary psychology
    • ethology, behaviour ecology
    • cross cultural psychology, anthropology, ethnology
    • Linguistics
  • guiding principle: compare and contrast
  • theoretical foundations: natural selection and culture
18
Q

Objective of nested designs

A
  • allows us to test 2 things:
    1. Difference between control and study areas
    2. The variability of the sites WITHIN ares
  • if we fail to find a significant variability Among the sites within areas, and find a significant different between areas, we would know there is an environmental impact
  • but it is likely that you WOULD find variability within the sites of one area
  • if so, you can still test to see whether the difference between the areas is significantly larger than the variability among sites within areas.
19
Q

What is nested

A
  • nesting tasks
  • nesting groups (naturally occurring groups)
  • nesting locations, sites, areas (naturally occurring sites)
  • nesting times (centuries, decades, years, seasons, months etc)
20
Q

Time series designs

A
  • basic time series with intervention:
    • multiple observations before and after treatment, and observation during treatment

-interrupted time series: same but with naturally occurring event… often taking something away

21
Q

Time series design variations

A
  • give treatment early, then cancel it and see effects
    • must consider carryover effects
    • cancellation of drugs cold turkey can be dangerous … discovered through time series

-follow typical ABA design (or variations of this theme)

22
Q

No equivalent control group design

A
  • using time series design but two separate groups:
    • one that receives treatment, and one that doesn’t
    • still need similar groups (matching) for internal validity
23
Q

Pre-test/post-test designs

A
  • true experimental design, similar to within-subject
    • two levels: pre and post treatment
  • carryover can be a problem
    • must have control groups and random assignment if possible
  • pre test should be same for both conditions, only post test should yield different results
  • problem: effect of having experienced pre-test may affect results
    • two solutions:
      1. Eliminate pre-test completely
      2. Solomon 4-group design: partial removal of pre-test to evaluate if there is an effect of the pre-test
      • if results from all groups are different you know there is a pre-test affect