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risk
probability that harm will occur
calculate the incidence rate
cohort study design
compares exposed & not exposed groups
participants selected on exposure status, not outcome
followed over time to see who develops outcome
start with healthy people
relative risk
[incidence rate in exposed]/[incidence rate in non-exposed]
case-control study design
start by identifying cases, then find healthy controls
compares past exposures in cases & controls (retrospective)
odds ratio
[odds of exposure in cases]/[odds of exposure in controls]
concurrent
at the same time
intention to treat
analyzing participants in the groups to which they were originally randomized, regardless of whether they adhered to assigned treatment
prognostic factor
characteristic that is strongly associated with an outcome
quasi-experimental design
subjects are not randomly assigned to treatments
protective factor
decreases the likelihood of a negative health outcome