Evidence map›Paper›PMID 41823059›Full record

ArticleStatistical methods in medical research2026

Efficient design of partially nested randomized trials: A maximin approach.

Math Jjm Candel, Gerard Jp van Breukelen

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

2 authors.

Math Jjm CandelDepartment of Methodology and Statistics, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-2229-1131
Gerard Jp van BreukelenDepartment of Methodology and Statistics, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands.ORCID 0000-0003-0949-0272

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For two-treatment randomized trials with clustering in one of the treatment arms and a continuous outcome, designs are presented that minimize the number of subjects or the amount of research budget, when aiming for a desired power level. These designs optimize the treatment-to-control allocation ratio of study participants but also optimize the choice between the number of clusters (such as therapy groups) versus the number of persons per cluster (therapy group) in the arm with clustering. Optimal designs require prior knowledge of parameters from the analysis model, which are unknown during the design stage. We present maximin designs which address this by ensuring a pre-specified power level for plausible ranges of the unknown parameters, while maximizing the power for worst-case values of these parameters. Maximin designs are also derived when the number of clusters, or the cluster size is fixed due to practical constraints. An empirical example illustrates how to calculate sample sizes for such practical designs and shows how much these maximin designs can reduce the required research budgets compared to designs with equal subject numbers in treatment and control. A user-friendly R Shiny app facilitates these sample size calculations.

Indexed as

Randomized Controlled Trials as TopicResearch DesignCluster AnalysisHumansModels, StatisticalSample SizeEfficient designindividually randomized group treatment trialspartially nested randomized trialspowersample size calculation

Identifiers

PMID41823059
PMCPMC13161498

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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.