Evidence map›Paper›PMID 38837431›Full record

ArticleStatistics in medicine2024

Robust analysis of stepped wedge trials using composite likelihood models.

Emily C Voldal, Avi Kenny, Fan Xia, Patrick Heagerty, James P Hughes

Abstract read
In one paragraph

Article in Statistics in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Emily C VoldalFred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-6286-3982
Avi KennyDepartment of Biostatistics & Bioinformatics, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-9465-7307
Fan XiaDepartment of Epidemiology & Biostatistics, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0002-2435-794X
Patrick HeagertyDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-3403-6007
James P HughesDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-5034-3157

Funding

NIH Health Care Systems Research Collaboratory-Coordinating Center (U24)U24AT009676 · NCCIH · DUKE UNIVERSITY · PI LESLEY H CURTIS, Adrian Hernandez · 2017 to 2026
$21.5M
STATISTICAL ISSUES IN AIDS RESEARCHR37AI029168 · NIAID · UNIVERSITY OF WASHINGTON · PI JAMES P HUGHES · 1999 to 2026
$9.8M
UW Core Center for Clinical Research of Musculoskeletal ConditionsP30AR072572 · NIAMS · UNIVERSITY OF WASHINGTON · PI JEFFREY G JARVIK, Pradeep Suri · 2017 to 2026
$8.3M
HEAL Collaboratory Resource Coordinating Center (PRISM) (U24): Bioethics SupplementU24AT010961 · NCCIH · DUKE UNIVERSITY · PI CURTIS, LESLEY H, HERNANDEZ, ADRIAN · 2019 to 2021
$6.4M
STATISTICAL ISSUES IN AIDS RESEARCHR01AI029168 · NIAID · UNIVERSITY OF WASHINGTON · PI HUGHES, JAMES P · 1989 to 2018
$5.3M
NCCIH NIH HHS U24 AT009676NCCIH NIH HHS U24 AT010961NIAID NIH HHS R01 AI029168NIAID NIH HHS R37 AI029168NIAMS NIH HHS P30 AR072572NIAMS NIH HHS P30AR072572NIH HHS AI029168
6 · The paper itself

Abstract

Stepped wedge trials (SWTs) are a type of cluster randomized trial that involve repeated measures on clusters and design-induced confounding between time and treatment. Although mixed models are commonly used to analyze SWTs, they are susceptible to misspecification particularly for cluster-longitudinal designs such as SWTs. Mixed model estimation leverages both "horizontal" or within-cluster information and "vertical" or between-cluster information. To use horizontal information in a mixed model, both the mean model and correlation structure must be correctly specified or accounted for, since time is confounded with treatment and measurements are likely correlated within clusters. Alternative non-parametric methods have been proposed that use only vertical information; these are more robust because between-cluster comparisons in a SWT preserve randomization, but these non-parametric methods are not very efficient. We propose a composite likelihood method that focuses on vertical information, but has the flexibility to recover efficiency by using additional horizontal information. We compare the properties and performance of various methods, using simulations based on COVID-19 data and a demonstration of application to the LIRE trial. We found that a vertical composite likelihood model that leverages baseline data is more robust than traditional methods, and more efficient than methods that use only vertical information. We hope that these results demonstrate the potential value of model-based vertical methods for SWTs with a large number of clusters, and that these new tools are useful to researchers who are concerned about misspecification of traditional models.

Indexed as

Cluster AnalysisComputer SimulationLikelihood FunctionsRandomized Controlled Trials as TopicResearch DesignCOVID-19Diagnostic ImagingHumansMulticenter Studies as TopicReproducibility of ResultsStatistics, NonparametricTime Factorscluster randomized trialscomposite likelihoodsmixed effects modelsrobust inferencestepped wedgevertical estimators

Identifiers

PMID38837431
PMCPMC11257102

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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.