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Design and analysis of trials with a partially nested design and a binary outcome measure
Where treatments are administered to groups of patients or delivered by therapists, outcomes for patients in the same group or treated by the same therapist may be more similar, leading to clustering. Trials of such treatments should take account of this effect. Where such a treatment is compared wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949566/ https://www.ncbi.nlm.nih.gov/pubmed/26670388 http://dx.doi.org/10.1002/sim.6828 |
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author | Roberts, Chris Batistatou, Evridiki Roberts, Stephen A. |
author_facet | Roberts, Chris Batistatou, Evridiki Roberts, Stephen A. |
author_sort | Roberts, Chris |
collection | PubMed |
description | Where treatments are administered to groups of patients or delivered by therapists, outcomes for patients in the same group or treated by the same therapist may be more similar, leading to clustering. Trials of such treatments should take account of this effect. Where such a treatment is compared with an un‐clustered treatment, the trial has a partially nested design. This paper compares statistical methods for this design where the outcome is binary. Investigation of consistency reveals that a random coefficient model with a random effect for group or therapist is not consistent with other methods for a null treatment effect, and so this model is not recommended for this design. Small sample performance of a cluster‐adjusted test of proportions, a summary measures test and logistic generalised estimating equations and random intercept models are investigated through simulation. The expected treatment effect is biased for the logistic models. Empirical test size of two‐sided tests is raised only slightly, but there are substantial biases for one‐sided tests. Three formulae are proposed for calculating sample size and power based on (i) the difference of proportions, (ii) the log‐odds ratio or (iii) the arc‐sine transformation of proportions. Calculated power from these formulae is compared with empirical power from a simulations study. Logistic models appeared to perform better than those based on proportions with the likelihood ratio test performing best in the range of scenarios considered. For these analyses, the log‐odds ratio method of calculation of power gave an approximate lower limit for empirical power. © 2015 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. |
format | Online Article Text |
id | pubmed-4949566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49495662016-07-28 Design and analysis of trials with a partially nested design and a binary outcome measure Roberts, Chris Batistatou, Evridiki Roberts, Stephen A. Stat Med Research Articles Where treatments are administered to groups of patients or delivered by therapists, outcomes for patients in the same group or treated by the same therapist may be more similar, leading to clustering. Trials of such treatments should take account of this effect. Where such a treatment is compared with an un‐clustered treatment, the trial has a partially nested design. This paper compares statistical methods for this design where the outcome is binary. Investigation of consistency reveals that a random coefficient model with a random effect for group or therapist is not consistent with other methods for a null treatment effect, and so this model is not recommended for this design. Small sample performance of a cluster‐adjusted test of proportions, a summary measures test and logistic generalised estimating equations and random intercept models are investigated through simulation. The expected treatment effect is biased for the logistic models. Empirical test size of two‐sided tests is raised only slightly, but there are substantial biases for one‐sided tests. Three formulae are proposed for calculating sample size and power based on (i) the difference of proportions, (ii) the log‐odds ratio or (iii) the arc‐sine transformation of proportions. Calculated power from these formulae is compared with empirical power from a simulations study. Logistic models appeared to perform better than those based on proportions with the likelihood ratio test performing best in the range of scenarios considered. For these analyses, the log‐odds ratio method of calculation of power gave an approximate lower limit for empirical power. © 2015 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2015-12-15 2016-05-10 /pmc/articles/PMC4949566/ /pubmed/26670388 http://dx.doi.org/10.1002/sim.6828 Text en © 2015 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Roberts, Chris Batistatou, Evridiki Roberts, Stephen A. Design and analysis of trials with a partially nested design and a binary outcome measure |
title | Design and analysis of trials with a partially nested design and a binary outcome measure |
title_full | Design and analysis of trials with a partially nested design and a binary outcome measure |
title_fullStr | Design and analysis of trials with a partially nested design and a binary outcome measure |
title_full_unstemmed | Design and analysis of trials with a partially nested design and a binary outcome measure |
title_short | Design and analysis of trials with a partially nested design and a binary outcome measure |
title_sort | design and analysis of trials with a partially nested design and a binary outcome measure |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949566/ https://www.ncbi.nlm.nih.gov/pubmed/26670388 http://dx.doi.org/10.1002/sim.6828 |
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