Evidence map›Paper›PMID 31228563›Full record

ArticleContemporary clinical trials2020

Impact of baseline covariate imbalance on bias in treatment effect estimation in cluster randomized trials: Race as an example.

Siyun Yang, Monique Anderson Starks, Adrian F Hernandez, Elizabeth L Turner, Robert M Califf, Christopher M O'Connor, Robert J Mentz, Kingshuk Roy Choudhury

Erratum issuedAbstract read
In one paragraph

Article in Contemporary clinical trials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Siyun YangDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, United States of America.
Monique Anderson StarksDepartment of Medicine, Duke University School of Medicine, Durham, NC, United States of America; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States of America. Electronic address: monique.starks@duke.edu.
Adrian F HernandezDepartment of Medicine, Duke University School of Medicine, Durham, NC, United States of America; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States of America.
Elizabeth L TurnerDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, United States of America; Duke Global Health Institute, Duke University, Durham, NC, United States of America.
Robert M CaliffDepartment of Medicine, Duke University School of Medicine, Durham, NC, United States of America; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States of America.
Christopher M O'ConnorInova Heart and Vascular Institute, Falls Church, VA, United States of America.
Robert J MentzDepartment of Medicine, Duke University School of Medicine, Durham, NC, United States of America; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States of America.
Kingshuk Roy ChoudhuryDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, United States of America.

Funding

Health Care Systems Research Collaboratory SupplementU54AT007748 · NCCIH · DUKE UNIVERSITY · PI CURTIS, LESLEY H, HERNANDEZ, ADRIAN · 2012 to 2017
$15.1M
NCCIH NIH HHS U54 AT007748
6 · The paper itself

Abstract

Individual-level baseline covariate imbalance could happen more frequently in cluster randomized trials, and may influence the observed treatment effect. Using computer and real-data simulations, this paper quantifies the extent and impact of covariate imbalance on the estimated treatment effect for both continuous and binary outcomes, and relates it to the degree of imbalance for different numbers of clusters, cluster sizes, and covariate intraclass correlation coefficients. We focused on the impact of race as a covariate, given the emphasis of regulatory and funding bodies on understanding the influence of demographic characteristics on treatment effectiveness. We found that bias in the treatment effect is proportional to both the degree of baseline covariate imbalance and the covariate effect size. Larger numbers of clusters result in lower covariate imbalance, and increasing cluster size is less effective in reducing imbalance compared to increasing the number of clusters. Models adjusted for important baseline confounders are superior to unadjusted models for minimizing bias in both model-based simulations and an innovative simulation based on real clinical trial data. Higher outcome intraclass correlation coefficients did not affect bias but resulted in greater variance in treatment estimates.

Indexed as

BiasMultivariate AnalysisRacial GroupsRandomized Controlled Trials as TopicCluster AnalysisComputer SimulationData Interpretation, StatisticalHumansTreatment OutcomeCluster analysis(MeSH terms): BiasMultivariable analysisRandomized controlled trials as topicResearch design

Identifiers

PMID31228563
PMCPMC8337048

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.