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Planning a method for covariate adjustment in individually randomised trials: a practical guide
BACKGROUND: It has long been advised to account for baseline covariates in the analysis of confirmatory randomised trials, with the main statistical justifications being that this increases power and, when a randomisation scheme balanced covariates, permits a valid estimate of experimental error. Th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014627/ https://www.ncbi.nlm.nih.gov/pubmed/35436970 http://dx.doi.org/10.1186/s13063-022-06097-z |
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author | Morris, Tim P. Walker, A. Sarah Williamson, Elizabeth J. White, Ian R. |
author_facet | Morris, Tim P. Walker, A. Sarah Williamson, Elizabeth J. White, Ian R. |
author_sort | Morris, Tim P. |
collection | PubMed |
description | BACKGROUND: It has long been advised to account for baseline covariates in the analysis of confirmatory randomised trials, with the main statistical justifications being that this increases power and, when a randomisation scheme balanced covariates, permits a valid estimate of experimental error. There are various methods available to account for covariates but it is not clear how to choose among them. METHODS: Taking the perspective of writing a statistical analysis plan, we consider how to choose between the three most promising broad approaches: direct adjustment, standardisation and inverse-probability-of-treatment weighting. RESULTS: The three approaches are similar in being asymptotically efficient, in losing efficiency with mis-specified covariate functions and in handling designed balance. If a marginal estimand is targeted (for example, a risk difference or survival difference), then direct adjustment should be avoided because it involves fitting non-standard models that are subject to convergence issues. Convergence is most likely with IPTW. Robust standard errors used by IPTW are anti-conservative at small sample sizes. All approaches can use similar methods to handle missing covariate data. With missing outcome data, each method has its own way to estimate a treatment effect in the all-randomised population. We illustrate some issues in a reanalysis of GetTested, a randomised trial designed to assess the effectiveness of an electonic sexually transmitted infection testing and results service. CONCLUSIONS: No single approach is always best: the choice will depend on the trial context. We encourage trialists to consider all three methods more routinely. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13063-022-06097-z). |
format | Online Article Text |
id | pubmed-9014627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90146272022-04-19 Planning a method for covariate adjustment in individually randomised trials: a practical guide Morris, Tim P. Walker, A. Sarah Williamson, Elizabeth J. White, Ian R. Trials Methodology BACKGROUND: It has long been advised to account for baseline covariates in the analysis of confirmatory randomised trials, with the main statistical justifications being that this increases power and, when a randomisation scheme balanced covariates, permits a valid estimate of experimental error. There are various methods available to account for covariates but it is not clear how to choose among them. METHODS: Taking the perspective of writing a statistical analysis plan, we consider how to choose between the three most promising broad approaches: direct adjustment, standardisation and inverse-probability-of-treatment weighting. RESULTS: The three approaches are similar in being asymptotically efficient, in losing efficiency with mis-specified covariate functions and in handling designed balance. If a marginal estimand is targeted (for example, a risk difference or survival difference), then direct adjustment should be avoided because it involves fitting non-standard models that are subject to convergence issues. Convergence is most likely with IPTW. Robust standard errors used by IPTW are anti-conservative at small sample sizes. All approaches can use similar methods to handle missing covariate data. With missing outcome data, each method has its own way to estimate a treatment effect in the all-randomised population. We illustrate some issues in a reanalysis of GetTested, a randomised trial designed to assess the effectiveness of an electonic sexually transmitted infection testing and results service. CONCLUSIONS: No single approach is always best: the choice will depend on the trial context. We encourage trialists to consider all three methods more routinely. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13063-022-06097-z). BioMed Central 2022-04-18 /pmc/articles/PMC9014627/ /pubmed/35436970 http://dx.doi.org/10.1186/s13063-022-06097-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Morris, Tim P. Walker, A. Sarah Williamson, Elizabeth J. White, Ian R. Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title | Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title_full | Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title_fullStr | Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title_full_unstemmed | Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title_short | Planning a method for covariate adjustment in individually randomised trials: a practical guide |
title_sort | planning a method for covariate adjustment in individually randomised trials: a practical guide |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014627/ https://www.ncbi.nlm.nih.gov/pubmed/35436970 http://dx.doi.org/10.1186/s13063-022-06097-z |
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