Cited by 258Statistical Methods in Clinical TrialsStatistical Methods in EpidemiologyAdvanced Causal Inference Techniques

Covariate adjustment in randomized controlled trials with dichotomous outcomes increases statistical power and reduces sample size requirements

Hernández, Adrián V, Steyerberg, Ewout W, Habbema, J.Dik F·2004·Journal of Clinical Epidemiology

Abstract

Objective Randomized controlled trials (RCTs) with dichotomous outcomes may be analyzed with or without adjustment for baseline characteristics (covariates). We studied type I error, power, and potential reduction in sample size with several covariate adjustment strategies.Study design and setting Logistic regression analysis was applied to simulated data sets (n=360) with different treatment effects, covariate effects, outcome incidences, and covariate prevalences. Treatment effects were estimated with or without adjustment for a single dichotomous covariate. Strategies included always adjusting for the covariate ("prespecified"), or only when the covariate was predictive or imbalanced.Results We found that the type I error was generally at the nominal level. The power was highest with prespecified adjustment. The potential reduction in sample size was higher with stronger covariate effects (from 3 to 46%, at 50% outcome incidence and covariate prevalence) and independent of the treatment effect. At lower outcome incidences and/or covariate prevalences, the reduction was lower.Conclusion We conclude that adjustment for a predictive baseline characteristic may lead to a potentially important increase in power of analyses of treatment effect. Adjusted analysis should, hence, be considered more often for RCTs with dichotomous outcomes.

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Crossref · 10.1016/j.jclinepi.2003.09.014

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  • Under an unconfounded experimental design with batches containing both controls and cases, batch effects can be removed by adding a batch covariate to the regression model, and this increases power compared to non-batch corrected analyses.

    “However, under the assumptions of an unconfounded experimental design with batches containing both controls and cases, batch effects can be removed by adding a batch covariate to the regression model71. This increases the power compared to non-batch corrected analyses72–74.”

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References 36 · Cited by 258

Authors
Hernández, A. V., Steyerberg, E. W., & Habbema, J. D. F.
Affiliations
Erasmus MC (NL)
Venue
Journal of Clinical Epidemiology
Publisher
Elsevier BV
Published
2004-05
Volume
57
Issue
5
Pages
454-460
ISSN
0895-4356 (ISSN-L)
OpenAlex
W2062383335
Cited by
258
References
36
Citations by year
2026: 11 · 2025: 15 · 2024: 14 · 2023: 13 · 2022: 21 · 2021: 32 · 2020: 20 · 2019: 8 · 2018: 12 · 2017: 9 · 2016: 9 · 2015: 12 · 2014: 13 · 2013: 15 · 2012: 11
FWCI
3.05
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Clinical Epidemiology (publishedVersion)
  • PubMed (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
Funders
Koninklijke Nederlandse Akademie van Wetenschappen
Topics
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
  • Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Epidemiology
  • Physical Sciences › Mathematics › Statistics and Probability › Advanced Causal Inference Techniques
Keywords
covariate adjustment, baseline characteristics, binary outcomes, statistical power, sample size reduction, type I error, logistic regression, treatment effect estimation
MeSH terms
Data Interpretation, Statistical, Humans, Research Design, Logistic Models, Randomized Controlled Trials as Topic, Treatment Outcome, Sample Size

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