Evidence
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When trial participation depends on observed covariates, propensity-score-based approaches can reweight the trial sample to resemble a target population, thereby generalizing estimated treatment effects beyond the original study sample.
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On variance estimation for generalizing from a trial to a target population ↗
Randomized controlled trials (RCTs) provide strong internal validity compared with observational studies. However, selection bias threatens the external validity of randomized trials. Thus, RCT results may not apply to either broad public policy populations or narrow populations, such as specific in…
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Randomized controlled trials (RCTs) provide strong internal validity compared with observational studies. However, selection bias threatens the external validity of randomized trials. Thus, RCT results may not apply to either broad public policy populations or narrow populations, such as specific insurance pools. Some researchers use propensity scores (PSs) to generalize results from an RCT to a target population. In this scenario, a PS is defined as the probability of participating in the trial conditioning on observed covariates. We study a model-free inverse probability weighted estimator (IPWE) of the average treatment effect in a target population with data from a randomized trial.