Evidence map›Paper›PMID 21335590›Full record

ArticleClinical trials (London, England)2011

Comparison of dynamic block randomization and minimization in randomized trials: a simulation study.

Lan Xiao, Phillip W Lavori, Sandra R Wilson, Jun Ma

Abstract readComparative Study
In one paragraph

Article in Clinical trials (London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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  15. Randomisation can do many things - but it cannot "fail".Significance (Oxford, England) · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. MACT: a manageable minimization allocation system.Computational and mathematical methods in medicine · 2014
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Lan XiaoDepartment of Health Services Research, Palo Alto Medical Foundation Research Institute, Palo Alto, CA, USA.
Phillip W Lavori
Sandra R Wilson
Jun Ma

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Stanford Center for Clinical and Translational Education and Research (SCCTER)UL1UL1RR025744 · NCRR · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 2008 to 2011
$22.4M
Can diet- & exercise-induced weight loss improve asthma control in obese adults?R01HL094466 · NHLBI · PALO ALTO MEDICAL FOUNDATION RES INST · PI MA, JUN · 2009 to 2013
$4.0M
Does Shared Decision-Making Improve Asthma Outcomes?R01HL067092 · NHLBI · KAISER FOUNDATION RESEARCH INSTITUTE · PI BUIST, ALINE SONIA · 2001 to 2005
$3.0M
Does Shared Decision-Making Improve Adherence in Asthma?R01HL069358 · NHLBI · PALO ALTO MEDICAL FOUNDATION RES INST · PI WILSON, SANDRA R · 2001 to 2004
$2.2M
NCATS NIH HHS UL1 TR001085NCI NIH HHS P30 CA124435NCRR NIH HHS UL1 RR025744NHLBI NIH HHS R01 HL067092NHLBI NIH HHS R01 HL069358NHLBI NIH HHS R01 HL094466NHLBI NIH HHS R01HL094466NHLBI NIH HHS R01HL69358NHLBI NIH HHS R18HL67092
6 · The paper itself

Abstract

backgroundMinimizing the imbalance of key baseline covariates between treatments is known to be very important to the precision of the estimate of treatment effect in clinical research. Dynamic randomization allocation techniques have been used to achieve balance across multiple baseline characteristics. However, empirical data are limited on how these techniques compare in terms of balance and efficiency. We are motivated by a newly funded randomized controlled trial, in which we have the option of choosing between two methods of randomization at the subject level: (1) randomizing individual subjects consecutively as they are enrolled, using Pocock and Simon's minimization method, and (2) simultaneously randomizing blocks of subjects once all subjects in a block have been enrolled, using a balance algorithm originally developed for cluster randomized trials. PURPOSE: To compare dynamic block randomization and minimization in terms of balance on baseline covariates and statistical efficiency. Simple randomization was included as a reference.

methodsA simulation study using data from a previous randomized controlled trial was conducted to compare balance statistics and the accuracy and power of hypothesis testing among the randomization methods.

resultsDynamic block randomization consistently produced the best balance and highest power for various sample and treatment effect sizes, even after post-adjustment of the pre-specified baseline covariates in all three methods. Consistent with previous reports, minimization performed better in balance and power than simple randomization; however, the differences were noticeably smaller compared to those between dynamic block randomization and simple randomization. LIMITATIONS: In this simulation study, we considered three sample sizes and two block sizes for a two-arm randomized trial. We assumed no interactions among the multiple baseline covariates. It is necessary to evaluate how the results may vary when the simulation conditions are changed before drawing broader conclusions regarding comparisons between the randomization methods.

conclusionsThis study demonstrates that dynamic block randomization outperforms minimization with regard to achieving balance and maximizing efficiency. Nevertheless, the differences across the three randomization strategies are modest. The statistical advantages associated with dynamic block randomization need to be considered in relation to the planned sample size and the practical issues for its implementation in deciding the preferred method of randomization for a given trial (e.g., the time required to accrue blocks of subjects of adequate size as balanced against the need to commence intervention/treatment immediately in those randomized to that experimental condition).

Indexed as

Computer SimulationMultivariate AnalysisAlgorithmsCluster AnalysisHumansRandomized Controlled Trials as TopicResearch DesignSample Size

Identifiers

PMID21335590
PMCPMC4296975

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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.