Quant Midterm Flashcards
(22 cards)
Baron & Kenney: 4 statistical criteria for mediation?
- Predictor variable significantly associated w outcome variable
- Predictor variable significantly associated w mediator
- Mediator significantly associated w outcome variable
- Previously significant relationship btwn predictor and outcome diminished once effects of mediator are controlled
Can be tested w regression equations
Define mediation
Explanatory link in relationship between 2 other variables
How, or by what means, does x affect y through one or more intervening variables, m
Define moderation
Factor that gives info about under why conditions and for whom the main effect exists. A factor that may alter the main effect
Two main types of sampling?
Probability sampling: occurs when sample is selected from the population w each member having equal probability of being included in the sample.
Convenience (non probability) sampling: chosen for ease of access
Quota sampling
Non probability sample in which researcher selects people according to a fixed quota. Aims to represent major characteristics of population by sampling proportional amount of each.
Clinicians illusion
Inherent confounding variable is duration of illness: clinicians sample is skewed right
Clinicians see prevalence (those currently suffering) vs incidence (first onset)
Not representative of full range of disease, bc clinical settings tend to comprise people w longer duration of illness and repeated episodes
Baron & Kenney approach to mediation an moderation
Moderation: m is a moderator if m explains under which conditions a is related to o (ie there is a significant interaction btwn m and a)
Mediation: m is a mediator if it helps explain how or why a is related to o (assumes no interaction btwn a and o)
MacArthur approach to mediation and moderation
Moderation: sig interaction btwn m and a. m must precede a and m and o must be independent (moderator cannot be associated w outcome)
Mediation: m must precede a. Sig interaction btwn m and a OR main effect of m without association btwn m and a.
Baron & Kenney vs. MacArthur
B&k do not assume interaction in mediation. Assuming interaction is zero may cause part of interaction effect to be remapped into main effects or error, increasing probability of type I or ii error. Also assumes causal pathways are known. Theory informs identification of mediators vs moderators.
MacArthur requires temporal precedence to make causal inference. Interaction term is always included: bc obvservational methods cannot assume causality, you cannot know whether a variable is a mediator or moderator. Bc of this, approach cannot be used in cross sectional or retrospective atudies
Efficacy studies
Higher internal validity
Focus on measuring specific effects of a specific intervention
Effectiveness studies
Higher external validity
Focus on generalizability: will this treatment work across settings?
Experimental studies
Direct manipulation of iv presumed to be causal agent
Assessment of an outcome thought to directly vary as a function of that iv (causal agent)
Some ethos of inferring what outcome could be wo causal agent (control)
Why randomize?
Joint source population: population from which you are inferring results about dv is theoretically the same in all conditions
Extraneous variables not directly measured (confounders) cannot be the cause of a sig relationship btwn x and y bc they should be equally distributed among all conditions
What aspect of experimental design allows us to say x is a sufficient cause of y?
Temporal relationship: deliberate manipulation of x means it came before y and was sufficient to cause y
What aspect of experimental design allows us to say x was necessary cause of y?
Control group of condition: since control did not get y, x was necessary.
How do you address randomization in a within subjects design?
Counterbalancing: by randomizing orders of condition, you minimize ordering effects. Order cannot be the reason x is related to y
Define a quasi experimental study
Causal inference vs causality
Like randomized experiments, but wo full control to randomize participants to exposure and non exposure conditions
Certain things cannot be manipulated by the researcher but can still happen in time and space and be captured in a study
Cohort vs case control studies
Cohort: selection of participants based on exposure status (iv)
Case control: selection based on outcome variable (DV)
Prospective cohort study
Exposure status obtained and measured at start. Group followed in time to ascertain disorder or outcome of interest.
Useful when interested in developmental timing of risk.
Limits recall bias
Retrospective cohort study
Group identified based on some exposure that occurred in past, then outcome is ascertained.
All history is traced in past–can be done w archival data.
Car control study
Quasi experimental study in which selection criteria is based on outcome variable, ie disease. Controls are wo disease.
Proportion of those exposed to risk factor should be higher in cases than controls.
Want newly diagnosed cases to avoid clinicians illusion.
Control group should be obtained independent of exposure status, should have equal chance of exposure risk.
Confounding can be dealt w statistically, through matching
Internal validity
Extent to which study minimizes systematic error (biases in measurement)
Threats include: History Maturation Experimenter expectancy Subject demand characteristics