A review found small variable blocking schemes may not protect against selection bias in randomized controlled trials.

Allocation concealment Bias Methodology Randomization Randomized controlled trials Research design

Journal

Journal of clinical epidemiology
ISSN: 1878-5921
Titre abrégé: J Clin Epidemiol
Pays: United States
ID NLM: 8801383

Informations de publication

Date de publication:
01 2022
Historique:
received: 10 04 2021
revised: 06 08 2021
accepted: 07 09 2021
pubmed: 15 9 2021
medline: 9 4 2022
entrez: 14 9 2021
Statut: ppublish

Résumé

Blocking is associated with prediction of the allocation sequence and subversion. This paper explores if blocking strategies lead to an increase in baseline age heterogeneity (a marker for potential subversion) and, whether the use of blocking is changing over time. The British Medical Journal, Journal of the American Medical Association, The Lancet and the New England Journal of Medicine were hand searched to identify open RCTs published in January between 2001 and 2020. To explore heterogeneity of baseline age meta-analyses were performed on trials implementing blocking, minimization, and simple randomization. One hundred seventy-nine open RCTs were identified: nine (5.0%) undertook simple randomization, 104 (58.1%) blocking, 25 (13.9%) minimization, and one (0.6%) both. Baseline age heterogeneity of 24% (P= 0.02) was observed in all trials implementing blocking, 62% (P = 0.001) in trials implementing a fixed block of four, 40% (P = 0.07) implementing variable blocks including a 2 and 0% for both simple randomization and minimization. Small block sizes are implemented in modern trials. Variable block sizes including two are associated with subversion and should not be implemented. If center only stratification is necessary, it should be used alongside larger blocking schemes. Authors should consider alternative methods to restrict randomization.

Identifiants

pubmed: 34520850
pii: S0895-4356(21)00289-4
doi: 10.1016/j.jclinepi.2021.09.009
pii:
doi:

Types de publication

Journal Article Meta-Analysis Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-98

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Laura Clark (L)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom. Electronic address: laura.clark@york.ac.uk.

Lauren Burke (L)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom.

Rachel Margaret Carr (R)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom.

Elizabeth Coleman (E)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom.

Gareth Roberts (G)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom.

David J Torgerson (DJ)

York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, United Kingdom.

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Classifications MeSH