Evidence map›Paper›PMID 34897793›Full record

ArticleBiometrical journal. Biometrische Zeitschrift2022

Power considerations for generalized estimating equations analyses of four-level cluster randomized trials.

Xueqi Wang, Elizabeth L Turner, John S Preisser, Fan Li

Abstract read
In one paragraph

Article in Biometrical journal. Biometrische Zeitschrift, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Modeling multivariate ordinal time series.Journal of applied statistics · 2026
    Article
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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

4 authors.

Xueqi WangDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-9449-5451
Elizabeth L TurnerDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-7638-5942
John S PreisserDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0002-7869-2057
Fan LiDepartment of Biostatistics, Yale University School of Public Health, New Haven, CT, USA.ORCID 0000-0001-6183-1893

Funding

RESHAPE Diversity SupplementR01MH120649 · NIMH · GEORGE WASHINGTON UNIVERSITY · PI KOHRT, BRANDON ALAN · 2019 to 2023
$3.5M
NIMH NIH HHS R01 MH120649
6 · The paper itself

Abstract

In this article, we develop methods for sample size and power calculations in four-level intervention studies when intervention assignment is carried out at any level, with a particular focus on cluster randomized trials (CRTs). CRTs involving four levels are becoming popular in healthcare research, where the effects are measured, for example, from evaluations (level 1) within participants (level 2) in divisions (level 3) that are nested in clusters (level 4). In such multilevel CRTs, we consider three types of intraclass correlations between different evaluations to account for such clustering: that of the same participant, that of different participants from the same division, and that of different participants from different divisions in the same cluster. Assuming arbitrary link and variance functions, with the proposed correlation structure as the true correlation structure, closed-form sample size formulas for randomization carried out at any level (including individually randomized trials within a four-level clustered structure) are derived based on the generalized estimating equations approach using the model-based variance and using the sandwich variance with an independence working correlation matrix. We demonstrate that empirical power corresponds well with that predicted by the proposed method for as few as eight clusters, when data are analyzed using the matrix-adjusted estimating equations for the correlation parameters with a bias-corrected sandwich variance estimator, under both balanced and unbalanced designs.

Indexed as

Research DesignBiasCluster AnalysisComputer SimulationHumansRandomized Controlled Trials as TopicSample Sizecluster randomized trialseigenvaluesextended nested exchangeable correlationmatrix-adjusted estimating equations (MAEE)sample size

Identifiers

PMID34897793
PMCPMC9574475

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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.