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Ch. 9-12
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Experiment
Designed to identify causal relationships;
we have the power to assign participants to an intervention
Observational studies
Identify associations that may signal causation;
we can only observe what participants choose to do
Confounder
Explains why two outcomes may correlate, but not be causally linked;
truly causes in/direct change in the response variable;
linked to explanatory variable, but not necessarily causally;
linked to both cause and effect
Mediating variable
Mediator between cause and effect;
links two things
Stratification
Breaking down comparison groups to control for confounders;
if differences still exist after stratification, argument for causality can begin to be built
Cross-sectional studies
Collect response and explanatory variable at a single point in a participant’s life
Cohort studies
Participants have an explanatory outcome, and then response outcomes are collected later;
typically prospective — response variable data is not available until later
Case-control studies
Participants are identified by their response outcomes, then data for explanatory outcomes is collected separately;
typically retrospective — explanatory variable data not available until later
Weakness of experiments, cross-sectional and cohort studies
If studying a rare incidence response outcome, we may need a very large sample size in order to estimate true risk with reasonable precision;
case-control studies can go straight to picking people with the rare outcome, bypassing this weakness
Odds ratio
Used instead of relative risk in cases like case-control studies;
not affected by non-natural incidence sampling;
tends to exaggerate
Blinded
Participants don’t know what group they are in
Double blinding
Neither the participants nor the people administering the intervention know what group they are in
Single group pre-post design
Control/intervention → Pre-measure → Treatment intervention → Post-measure;
Placebo effect and test familiarity are threats
Multiple group design
Separate treatment/control;
Treatment intervention → Response measure OR
Control (intervention) → Response measure
Random assignment w/ blocking
Units are blocked by potential confounders before random assignment into groups;
Helps assure equivalent groups when sample sizes are small
Non-randomized controlled experiment
Uses a non-random assignment method;
may create bias
Randomized controlled experiment with repeated measures
Take multiple measures per person at different time points;
may present a test familiarity threat
Randomized controlled experiments with crossover measures
Special case of repeated measures;
Each group completes both experimental conditions and produce response measures from both;
Need to be wary of lingering measures — may have buffer time between
Causality threats
Group selection
Drop out differences
Test familiarity
Timing effects
Setting effects
Independence
Group selection (threat)
If groups are being compared, they should be similar/equivalent
Drop out differences
Attrition/mortality → dropouts;
Threaten causality argument when drop out rates are different or the reasons for dropping out are different;
When there is some level of attrition due to non-adherence, researchers may make a comparison of all intent-to-treat participants
Setting effects
Placebo effect
Researcher effects
Environment condition differences
Sample biases in random sampling
Undercoverage bias
Volunteer bias
Undercoverage bias
Some in the population don’t have an equal chance or have no chance to be selected
Volunteer bias
Once selected, those who chose to participate may be systematically different than those who chose not to participate (self-select) or forgot to/are unable to respond (non-response)
Survivorship bias
Especially important in biomedical studies;
Sampling process results in an inaccurate number of un/successful cases that don’t represent the population
Convenience sampling
Non-random sampling plan
Quota sampling
Identifies key features we want to represent and tries to sample a target number from each subgroup
Weighted sampling
Attempts to use a mathematical model to weigh for subgroups that are under/overrepresented
3 types of uncertainty
Causality
Generalizability
Precision
Statistical power
How much we have reduced our uncertainty in precision
Two ways to improve statistical power
Increase sample size
Decrease random sources of variation
+ dividing sample size equally has a small effect
Abstract
150-300 word summary of a research paper
Four parts of research process
Problem
Design
Analysis
Conclusions