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HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention

The rigorous evaluation of the impact of combination HIV prevention packages at the population level will be critical for the future of HIV prevention. In this review, we discuss important considerations for the design and interpretation of cluster randomized controlled trials (C-RCTs) of combinatio...

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Autores principales: Boily, Marie-Claude, Mâsse, Benoît, Alsallaq, Ramzi, Padian, Nancy S., Eaton, Jeffrey W., Vesga, Juan F., Hallett, Timothy B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393676/
https://www.ncbi.nlm.nih.gov/pubmed/22807657
http://dx.doi.org/10.1371/journal.pmed.1001250
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author Boily, Marie-Claude
Mâsse, Benoît
Alsallaq, Ramzi
Padian, Nancy S.
Eaton, Jeffrey W.
Vesga, Juan F.
Hallett, Timothy B.
author_facet Boily, Marie-Claude
Mâsse, Benoît
Alsallaq, Ramzi
Padian, Nancy S.
Eaton, Jeffrey W.
Vesga, Juan F.
Hallett, Timothy B.
author_sort Boily, Marie-Claude
collection PubMed
description The rigorous evaluation of the impact of combination HIV prevention packages at the population level will be critical for the future of HIV prevention. In this review, we discuss important considerations for the design and interpretation of cluster randomized controlled trials (C-RCTs) of combination prevention interventions. We focus on three large C-RCTs that will start soon and are designed to test the hypothesis that combination prevention packages, including expanded access to antiretroviral therapy, can substantially reduce HIV incidence. Using a general framework to integrate mathematical modelling analysis into the design, conduct, and analysis of C-RCTs will complement traditional statistical analyses and strengthen the evaluation of the interventions. Importantly, even with combination interventions, it may be challenging to substantially reduce HIV incidence over the 2- to 3-y duration of a C-RCT, unless interventions are scaled up rapidly and key populations are reached. Thus, we propose the innovative use of mathematical modelling to conduct interim analyses, when interim HIV incidence data are not available, to allow the ongoing trials to be modified or adapted to reduce the likelihood of inconclusive outcomes. The preplanned, interactive use of mathematical models during C-RCTs will also provide a valuable opportunity to validate and refine model projections.
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spelling pubmed-33936762012-07-17 HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention Boily, Marie-Claude Mâsse, Benoît Alsallaq, Ramzi Padian, Nancy S. Eaton, Jeffrey W. Vesga, Juan F. Hallett, Timothy B. PLoS Med Review The rigorous evaluation of the impact of combination HIV prevention packages at the population level will be critical for the future of HIV prevention. In this review, we discuss important considerations for the design and interpretation of cluster randomized controlled trials (C-RCTs) of combination prevention interventions. We focus on three large C-RCTs that will start soon and are designed to test the hypothesis that combination prevention packages, including expanded access to antiretroviral therapy, can substantially reduce HIV incidence. Using a general framework to integrate mathematical modelling analysis into the design, conduct, and analysis of C-RCTs will complement traditional statistical analyses and strengthen the evaluation of the interventions. Importantly, even with combination interventions, it may be challenging to substantially reduce HIV incidence over the 2- to 3-y duration of a C-RCT, unless interventions are scaled up rapidly and key populations are reached. Thus, we propose the innovative use of mathematical modelling to conduct interim analyses, when interim HIV incidence data are not available, to allow the ongoing trials to be modified or adapted to reduce the likelihood of inconclusive outcomes. The preplanned, interactive use of mathematical models during C-RCTs will also provide a valuable opportunity to validate and refine model projections. Public Library of Science 2012-07-10 /pmc/articles/PMC3393676/ /pubmed/22807657 http://dx.doi.org/10.1371/journal.pmed.1001250 Text en Boily et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Review
Boily, Marie-Claude
Mâsse, Benoît
Alsallaq, Ramzi
Padian, Nancy S.
Eaton, Jeffrey W.
Vesga, Juan F.
Hallett, Timothy B.
HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title_full HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title_fullStr HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title_full_unstemmed HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title_short HIV Treatment as Prevention: Considerations in the Design, Conduct, and Analysis of Cluster Randomized Controlled Trials of Combination HIV Prevention
title_sort hiv treatment as prevention: considerations in the design, conduct, and analysis of cluster randomized controlled trials of combination hiv prevention
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393676/
https://www.ncbi.nlm.nih.gov/pubmed/22807657
http://dx.doi.org/10.1371/journal.pmed.1001250
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