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Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study

PURPOSE: Over the last decade, many studies were performed regarding treatment options for hemorrhoidal disease. Randomised controlled trials (RCTs) should have well-defined primary and secondary outcomes. However, the reported outcome measures are numerous and diverse. The heterogeneity of outcome...

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Autores principales: van Tol, R. R., Melenhorst, J., Dirksen, C. D., Stassen, L. P. S., Breukink, S. O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486628/
https://www.ncbi.nlm.nih.gov/pubmed/28501943
http://dx.doi.org/10.1007/s00384-017-2833-5
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author van Tol, R. R.
Melenhorst, J.
Dirksen, C. D.
Stassen, L. P. S.
Breukink, S. O.
author_facet van Tol, R. R.
Melenhorst, J.
Dirksen, C. D.
Stassen, L. P. S.
Breukink, S. O.
author_sort van Tol, R. R.
collection PubMed
description PURPOSE: Over the last decade, many studies were performed regarding treatment options for hemorrhoidal disease. Randomised controlled trials (RCTs) should have well-defined primary and secondary outcomes. However, the reported outcome measures are numerous and diverse. The heterogeneity of outcome definition in clinical trials limits transparency and paves the way for bias. The development of a core outcome set (COS) helps minimizing this problem. A COS is an agreed minimum set of outcomes that should be measured and reported in all clinical trials of a specific disease. The aim of this project is to generate a COS regarding the outcome of treatment after hemorrhoidal disease. METHODS: A Delphi study will be performed by an international steering group healthcare professionals and patients with the intention to create a standard outcome set for future clinical trials for the treatment of hemorrhoidal disease. First, a literature review will be conducted to establish which outcomes are used in clinical trials for hemorrhoidal disease. Secondly, both healthcare professionals and patients will participate in several consecutive rounds of online questionnaires and a face-to-face meeting to refine the content of the COS. DISCUSSION: Development of a COS for hemorrhoidal disease defines a minimum outcome-reporting standard and will improve the quality of research in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00384-017-2833-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-54866282017-07-11 Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study van Tol, R. R. Melenhorst, J. Dirksen, C. D. Stassen, L. P. S. Breukink, S. O. Int J Colorectal Dis Clinical Study Protocol PURPOSE: Over the last decade, many studies were performed regarding treatment options for hemorrhoidal disease. Randomised controlled trials (RCTs) should have well-defined primary and secondary outcomes. However, the reported outcome measures are numerous and diverse. The heterogeneity of outcome definition in clinical trials limits transparency and paves the way for bias. The development of a core outcome set (COS) helps minimizing this problem. A COS is an agreed minimum set of outcomes that should be measured and reported in all clinical trials of a specific disease. The aim of this project is to generate a COS regarding the outcome of treatment after hemorrhoidal disease. METHODS: A Delphi study will be performed by an international steering group healthcare professionals and patients with the intention to create a standard outcome set for future clinical trials for the treatment of hemorrhoidal disease. First, a literature review will be conducted to establish which outcomes are used in clinical trials for hemorrhoidal disease. Secondly, both healthcare professionals and patients will participate in several consecutive rounds of online questionnaires and a face-to-face meeting to refine the content of the COS. DISCUSSION: Development of a COS for hemorrhoidal disease defines a minimum outcome-reporting standard and will improve the quality of research in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00384-017-2833-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-05-13 2017 /pmc/articles/PMC5486628/ /pubmed/28501943 http://dx.doi.org/10.1007/s00384-017-2833-5 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Clinical Study Protocol
van Tol, R. R.
Melenhorst, J.
Dirksen, C. D.
Stassen, L. P. S.
Breukink, S. O.
Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title_full Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title_fullStr Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title_full_unstemmed Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title_short Protocol for the development of a Core Outcome Set (COS) for hemorrhoidal disease: an international Delphi study
title_sort protocol for the development of a core outcome set (cos) for hemorrhoidal disease: an international delphi study
topic Clinical Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486628/
https://www.ncbi.nlm.nih.gov/pubmed/28501943
http://dx.doi.org/10.1007/s00384-017-2833-5
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