Evidence map›Paper›PMID 26282553›Full record

ReviewTrials2015

Sample size calculation for a stepped wedge trial.

Gianluca Baio, Andrew Copas, Gareth Ambler, James Hargreaves, Emma Beard, Rumana Z Omar

3 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Trials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 101 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 4 pooled it
16.8field-weighted citation impact, top 1% of its field
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.

NCT03243708 nacompletednot on this mapstarted 2017, after this paper: background citation

Title: EHR Embedded Risk Calculator vs. Standard VTE Prophylaxis for Medical Patients

TypeinterventionalSponsorThe Cleveland ClinicRan2017 to 2019Enrolled90,537ConditionsVenous ThromboembolismArmsRisk calculator
NCT04029454 nacompletednot on this mapstarted 2020, after this paper: background citation

Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vaccine Into the Infant Immunization Schedule: a Mixed Methods Study Including a Cluster-randomized Trial, an Anthropological Study and an Economic Evaluation

TypeinterventionalSponsorInstitut PasteurRan2020 to 2023Enrolled10,000ConditionsHepatitis BArmsbirth dose vaccination against hepatitis B strategy
NCT06018285 narecruitingnot on this mapstarted 2023, after this paper: background citation

Stepped Approach to Reducing Risk of Suicide in Primary Care

TypeinterventionalSponsorCynthia FontanellaRan2023 to 2027Enrolled2,572ConditionsSuicidal Ideation, Suicide, Attempted, Suicide PreventionArmsStepped Approach to Reducing Risk of Suicide in Primary Care
3 · Its place in the literature

Who cites it

101 citing papers in PubMed, 4 syntheses or guidelines pooled it, 161 citations in OpenAlex.

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41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Gianluca BaioDepartment of Statistical Science, University College London, Gower Street, London, UK. g.baio@ucl.ac.uk.
Andrew CopasMRC Clinical Trials Unit at University College London, CC, London, UK. a.copas@ucl.ac.uk.
Gareth AmblerDepartment of Statistical Science, University College London, Gower Street, London, UK. g.ambler@ucl.ac.uk.
James HargreavesDepartment of Social and Environmental Health Research, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK. james.hargreaves@lshtm.ac.uk.
Emma BeardDepartment of Clinical, Educational and Health Psychology, University College London, Gower Street, London, UK. e.beard@ucl.ac.uk.
Rumana Z OmarDepartment of Statistical Science, University College London, Gower Street, London, UK. r.omar@ucl.ac.uk.
University College London · GBLondon School of Hygiene & Tropical Medicine · GBMRC Clinical Trials Unit at UCL · GB

Funding

Medical Research Council MC_UU_12023/29Medical Research Council MR/K012126/1
6 · The paper itself

Abstract

backgroundStepped wedge trials (SWTs) can be considered as a variant of a clustered randomised trial, although in many ways they embed additional complications from the point of view of statistical design and analysis. While the literature is rich for standard parallel or clustered randomised clinical trials (CRTs), it is much less so for SWTs. The specific features of SWTs need to be addressed properly in the sample size calculations to ensure valid estimates of the intervention effect.

methodsWe critically review the available literature on analytical methods to perform sample size and power calculations in a SWT. In particular, we highlight the specific assumptions underlying currently used methods and comment on their validity and potential for extensions. Finally, we propose the use of simulation-based methods to overcome some of the limitations of analytical formulae. We performed a simulation exercise in which we compared simulation-based sample size computations with analytical methods and assessed the impact of varying the basic parameters to the resulting sample size/power, in the case of continuous and binary outcomes and assuming both cross-sectional data and the closed cohort design.

resultsWe compared the sample size requirements for a SWT in comparison to CRTs based on comparable number of measurements in each cluster. In line with the existing literature, we found that when the level of correlation within the clusters is relatively high (for example, greater than 0.1), the SWT requires a smaller number of clusters. For low values of the intracluster correlation, the two designs produce more similar requirements in terms of total number of clusters. We validated our simulation-based approach and compared the results of sample size calculations to analytical methods; the simulation-based procedures perform well, producing results that are extremely similar to the analytical methods. We found that usually the SWT is relatively insensitive to variations in the intracluster correlation, and that failure to account for a potential time effect will artificially and grossly overestimate the power of a study.

conclusionsWe provide a framework for handling the sample size and power calculations of a SWT and suggest that simulation-based procedures may be more effective, especially in dealing with the specific features of the study at hand. In selected situations and depending on the level of intracluster correlation and the cluster size, SWTs may be more efficient than comparable CRTs. However, the decision about the design to be implemented will be based on a wide range of considerations, including the cost associated with the number of clusters, number of measurements and the trial duration.

Indexed as

Sample SizeComputer SimulationData Interpretation, StatisticalHumansModels, StatisticalPatient SelectionRandomized Controlled Trials as TopicResearch DesignTime Factors

Identifiers

PMID26282553
PMCPMC4538764
OpenAlexW2101092363

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.