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Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study
BACKGROUND: Poor retention in randomised trials can lead to serious consequences to their validity. Studies within trials (SWATs) are used to identify the most effective interventions to increase retention. Many interventions could be applied at any follow-up time point, but SWATs commonly assess in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148456/ https://www.ncbi.nlm.nih.gov/pubmed/37118802 http://dx.doi.org/10.1186/s13063-023-07323-y |
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author | Goulao, Beatriz Duncan, Anne Innes, Karen Ramsay, Craig R. Kahan, Brennan C. |
author_facet | Goulao, Beatriz Duncan, Anne Innes, Karen Ramsay, Craig R. Kahan, Brennan C. |
author_sort | Goulao, Beatriz |
collection | PubMed |
description | BACKGROUND: Poor retention in randomised trials can lead to serious consequences to their validity. Studies within trials (SWATs) are used to identify the most effective interventions to increase retention. Many interventions could be applied at any follow-up time point, but SWATs commonly assess interventions at a single time point, which can reduce efficiency. METHODS: The re-randomisation design allows participants to be re-enrolled and re-randomised whenever a new retention opportunity occurs (i.e. a new follow-up time point where the intervention could be applied). The main advantages are as follows: (a) it allows the estimation of an average effect across time points, thus increasing generalisability; (b) it can be more efficient than a parallel arm trial due to increased sample size; and (c) it allows subgroup analyses to estimate effectiveness at different time points. We present a case study where the re-randomisation design is used in a SWAT. RESULTS: In our case study, the host trial is a dental trial with two available follow-up points. The Sticker SWAT tests whether adding the trial logo’s sticker to the questionnaire’s envelope will result in a higher response rate compared with not adding the sticker. The primary outcome is the response rate to postal questionnaires. The re-randomisation design could double the available sample size compared to a parallel arm trial, resulting in the ability to detect an effect size around 28% smaller. CONCLUSION: The re-randomisation design can increase the efficiency and generalisability of SWATs for trials with multiple follow-up time points. |
format | Online Article Text |
id | pubmed-10148456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101484562023-04-30 Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study Goulao, Beatriz Duncan, Anne Innes, Karen Ramsay, Craig R. Kahan, Brennan C. Trials Methodology BACKGROUND: Poor retention in randomised trials can lead to serious consequences to their validity. Studies within trials (SWATs) are used to identify the most effective interventions to increase retention. Many interventions could be applied at any follow-up time point, but SWATs commonly assess interventions at a single time point, which can reduce efficiency. METHODS: The re-randomisation design allows participants to be re-enrolled and re-randomised whenever a new retention opportunity occurs (i.e. a new follow-up time point where the intervention could be applied). The main advantages are as follows: (a) it allows the estimation of an average effect across time points, thus increasing generalisability; (b) it can be more efficient than a parallel arm trial due to increased sample size; and (c) it allows subgroup analyses to estimate effectiveness at different time points. We present a case study where the re-randomisation design is used in a SWAT. RESULTS: In our case study, the host trial is a dental trial with two available follow-up points. The Sticker SWAT tests whether adding the trial logo’s sticker to the questionnaire’s envelope will result in a higher response rate compared with not adding the sticker. The primary outcome is the response rate to postal questionnaires. The re-randomisation design could double the available sample size compared to a parallel arm trial, resulting in the ability to detect an effect size around 28% smaller. CONCLUSION: The re-randomisation design can increase the efficiency and generalisability of SWATs for trials with multiple follow-up time points. BioMed Central 2023-04-29 /pmc/articles/PMC10148456/ /pubmed/37118802 http://dx.doi.org/10.1186/s13063-023-07323-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Goulao, Beatriz Duncan, Anne Innes, Karen Ramsay, Craig R. Kahan, Brennan C. Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title | Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title_full | Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title_fullStr | Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title_full_unstemmed | Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title_short | Using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
title_sort | using re-randomisation designs to increase the efficiency and applicability of retention studies within trials: a case study |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148456/ https://www.ncbi.nlm.nih.gov/pubmed/37118802 http://dx.doi.org/10.1186/s13063-023-07323-y |
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