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

clinical trials covariate and response adaptive randomization crowdsourcing experimentation matching sequential experiments

Journal

Biometrics
ISSN: 1541-0420
Titre abrégé: Biometrics
Pays: United States
ID NLM: 0370625

Informations de publication

Date de publication:
Mar 2023
Historique:
revised: 09 06 2021
received: 14 10 2020
accepted: 07 09 2021
pubmed: 19 9 2021
medline: 19 9 2021
entrez: 18 9 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34535893
doi: 10.1111/biom.13561
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

216-229

Subventions

Organisme : United States-Israel Binational Science Foundation
ID : 2018112

Informations de copyright

© 2021 The International Biometric Society.

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Auteurs

Adam Kapelner (A)

Department of Mathematics, Queens College, CUNY, Queens, New York, USA.

Abba Krieger (A)

Department of Statistics, The Wharton School at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Classifications MeSH