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A matching procedure for sequential experiments that iteratively learns which covariates improve power.

Adam KapelnerAbba Krieger
Published in: Biometrics (2021)
We propose a dynamic allocation procedure that increases power and efficiency when measuring an average treatment effect in sequential randomized trials exploiting some subjects' previous assessed responses. Subjects arrive sequentially and are either randomized or paired to a previously randomized subject and administered the alternate treatment. The pairing is made via a dynamic matching criterion that iteratively learns which specific covariates are important to the response. We develop estimators for the average treatment effect as well as an exact test. We illustrate our method's increase in efficiency and power over other allocation procedures in both simulated scenarios and a clinical trial dataset. An R package "SeqExpMatch" for use by practitioners is available on CRAN.
Keyphrases
  • double blind
  • open label
  • randomized controlled trial
  • primary care
  • minimally invasive
  • phase ii
  • replacement therapy
  • combination therapy