Literature DB >> 3608506

The impact of treatment allocation procedures on nominal significance levels and bias.

L A Kalish, C B Begg.   

Abstract

Complete randomization, the simplest method for allocating treatments to patients in clinical trials, can serve as a basis for inferential procedures using standard permutation tests, because the method ensures that each sequence of allocations is equally likely. No other method of allocation possesses this property. However, many clinical trials employ allocation methods that force balance of covariates across treatment groups. With these methods, some allocation sequences are impossible or highly unlikely so that standard permutation tests are technically invalidated. In this article we investigate whether standard permutation tests for binary outcomes are likely to yield distorted nominal p values in practical applications of these alternative allocation methods. A sample of completed trials conducted by the Eastern Cooperative Oncology Group serves as a basis on which to construct simulations. Our results indicate that nominal p values can be conservative, but are not likely to be severely distorted if the analysis is stratified by important covariates used as allocation prompts. Moreover the inherent conservativeness of exact methods due to discreteness tends to dominate any additional conservativeness due to nonrandom designs. In addition, we investigate the relationship of treatment allocation methods with bias in estimates from a logistic model when important covariates are unknown. This bias is the same for all asymptotically balanced allocation methods and is significant but not disastrous.

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Year:  1987        PMID: 3608506     DOI: 10.1016/0197-2456(87)90037-7

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN: 0197-2456


  8 in total

Review 1.  How to randomize.

Authors:  Andrew J Vickers
Journal:  J Soc Integr Oncol       Date:  2006

2.  Impact of minimal sufficient balance, minimization, and stratified permuted blocks on bias and power in the estimation of treatment effect in sequential clinical trials with a binary endpoint.

Authors:  Steven D Lauzon; Wenle Zhao; Paul J Nietert; Jody D Ciolino; Michael D Hill; Viswanathan Ramakrishnan
Journal:  Stat Methods Med Res       Date:  2021-11-29       Impact factor: 2.494

3.  Statistical issues in the use of dynamic allocation methods for balancing baseline covariates.

Authors:  G R Pond
Journal:  Br J Cancer       Date:  2011-05-03       Impact factor: 7.640

4.  Randomization-based inference for a marginal treatment effect in stepped wedge cluster randomized trials.

Authors:  Dustin J Rabideau; Rui Wang
Journal:  Stat Med       Date:  2021-05-21       Impact factor: 2.497

Review 5.  Randomization in substance abuse clinical trials.

Authors:  Sarra L Hedden; Robert F Woolson; Robert J Malcolm
Journal:  Subst Abuse Treat Prev Policy       Date:  2006-02-06

6.  Cage allocation designs for rodent carcinogenicity experiments.

Authors:  A M Herzberg; S W Lagakos
Journal:  Environ Health Perspect       Date:  1991-12       Impact factor: 9.031

7.  Randomization in cancer clinical trials: permutation test and development of a computer program.

Authors:  Y Ohashi
Journal:  Environ Health Perspect       Date:  1990-07       Impact factor: 9.031

8.  Response-adaptive designs for binary responses: How to offer patient benefit while being robust to time trends?

Authors:  Sofía S Villar; Jack Bowden; James Wason
Journal:  Pharm Stat       Date:  2017-12-19       Impact factor: 1.894

  8 in total

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