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The proportion of randomized controlled trials that inform clinical practice
Prior studies suggest that clinical trials are often hampered by problems in design, conduct, and reporting that limit their uptake in clinical practice. We have described ‘informativeness’ as the ability of a trial to guide clinical, policy, or research decisions. Little is known about the proporti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427100/ https://www.ncbi.nlm.nih.gov/pubmed/35975784 http://dx.doi.org/10.7554/eLife.79491 |
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author | Hutchinson, Nora Moyer, Hannah Zarin, Deborah A Kimmelman, Jonathan |
author_facet | Hutchinson, Nora Moyer, Hannah Zarin, Deborah A Kimmelman, Jonathan |
author_sort | Hutchinson, Nora |
collection | PubMed |
description | Prior studies suggest that clinical trials are often hampered by problems in design, conduct, and reporting that limit their uptake in clinical practice. We have described ‘informativeness’ as the ability of a trial to guide clinical, policy, or research decisions. Little is known about the proportion of initiated trials that inform clinical practice. We created a cohort of randomized interventional clinical trials in three disease areas (ischemic heart disease, diabetes mellitus, and lung cancer) that were initiated between January 1, 2009 and December 31, 2010 using ClinicalTrials.gov. We restricted inclusion to trials aimed at answering a clinical question related to the treatment or prevention of disease. Our primary outcome was the proportion of clinical trials fulfilling four conditions of informativeness: importance of the clinical question, trial design, feasibility, and reporting of results. Our study included 125 clinical trials. The proportion meeting four conditions for informativeness was 26.4% (95% CI 18.9–35.0). Sixty-seven percent of participants were enrolled in informative trials. The proportion of informative trials did not differ significantly between our three disease areas. Our results suggest that the majority of randomized interventional trials designed to guide clinical practice possess features that may compromise their ability to do so. This highlights opportunities to improve the scientific vetting of clinical research. |
format | Online Article Text |
id | pubmed-9427100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-94271002022-08-31 The proportion of randomized controlled trials that inform clinical practice Hutchinson, Nora Moyer, Hannah Zarin, Deborah A Kimmelman, Jonathan eLife Medicine Prior studies suggest that clinical trials are often hampered by problems in design, conduct, and reporting that limit their uptake in clinical practice. We have described ‘informativeness’ as the ability of a trial to guide clinical, policy, or research decisions. Little is known about the proportion of initiated trials that inform clinical practice. We created a cohort of randomized interventional clinical trials in three disease areas (ischemic heart disease, diabetes mellitus, and lung cancer) that were initiated between January 1, 2009 and December 31, 2010 using ClinicalTrials.gov. We restricted inclusion to trials aimed at answering a clinical question related to the treatment or prevention of disease. Our primary outcome was the proportion of clinical trials fulfilling four conditions of informativeness: importance of the clinical question, trial design, feasibility, and reporting of results. Our study included 125 clinical trials. The proportion meeting four conditions for informativeness was 26.4% (95% CI 18.9–35.0). Sixty-seven percent of participants were enrolled in informative trials. The proportion of informative trials did not differ significantly between our three disease areas. Our results suggest that the majority of randomized interventional trials designed to guide clinical practice possess features that may compromise their ability to do so. This highlights opportunities to improve the scientific vetting of clinical research. eLife Sciences Publications, Ltd 2022-08-17 /pmc/articles/PMC9427100/ /pubmed/35975784 http://dx.doi.org/10.7554/eLife.79491 Text en © 2022, Hutchinson et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Medicine Hutchinson, Nora Moyer, Hannah Zarin, Deborah A Kimmelman, Jonathan The proportion of randomized controlled trials that inform clinical practice |
title | The proportion of randomized controlled trials that inform clinical practice |
title_full | The proportion of randomized controlled trials that inform clinical practice |
title_fullStr | The proportion of randomized controlled trials that inform clinical practice |
title_full_unstemmed | The proportion of randomized controlled trials that inform clinical practice |
title_short | The proportion of randomized controlled trials that inform clinical practice |
title_sort | proportion of randomized controlled trials that inform clinical practice |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427100/ https://www.ncbi.nlm.nih.gov/pubmed/35975784 http://dx.doi.org/10.7554/eLife.79491 |
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