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Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol

BACKGROUND: Maternal obesity is a risk factor for adverse maternal, fetal, and neonatal events. Numerous clinical trials are currently exploring the effectiveness of antenatal and peripartum interventions in improving pregnancy outcomes that can in future inform clinical practice. However, the heter...

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Autores principales: Dadouch, Rachel, Faheim, Mina, Juando-Prats, Clara, Parsons, Janet, D’Souza, Rohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258169/
https://www.ncbi.nlm.nih.gov/pubmed/30482249
http://dx.doi.org/10.1186/s13063-018-3029-1
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author Dadouch, Rachel
Faheim, Mina
Juando-Prats, Clara
Parsons, Janet
D’Souza, Rohan
author_facet Dadouch, Rachel
Faheim, Mina
Juando-Prats, Clara
Parsons, Janet
D’Souza, Rohan
author_sort Dadouch, Rachel
collection PubMed
description BACKGROUND: Maternal obesity is a risk factor for adverse maternal, fetal, and neonatal events. Numerous clinical trials are currently exploring the effectiveness of antenatal and peripartum interventions in improving pregnancy outcomes that can in future inform clinical practice. However, the heterogeneity in outcome reporting limits our ability to compare outcomes across studies, and there is a lack of stakeholder representation in outcome choice. A pragmatic solution to this problem is the development of a core outcome set (COS) that defines the minimum criteria for outcome reporting in clinical trials undertaken in this population, arrived at by the involvement of relevant stakeholders. METHODS: The development of a COS for studies on obesity in pregnant patients (COSSOPP) will comprise five steps. First, a systematic review of published literature will identify the long list of outcomes, their definitions and measurements if applicable, and outcome reporting quality. This will be followed by a meta-synthesis of qualitative studies with patients, and qualitative interviews in Toronto with patients, clinicians, researchers, hospital administrators, and policy-makers, to identify novel outcomes that were not obtained through systematic review. Third, the long list of outcomes will be narrowed down through online Delphi surveys involving an international group of patients and relevant stakeholders. This will be followed by a face-to-face consensus meeting with representatives of all stakeholder groups to arrive at a consensus on the final COS. Finally, in order to determine how the identified core outcomes should be measured, we will conduct another literature review and Delphi process. DISCUSSION: COSSOPP will engage patients, clinicians, researchers, and other relevant stakeholders in determining the core set of outcomes that should be reported and measured in order to harmonize outcome reporting in studies evaluating the effectiveness of antepartum and peripartum interventions in obese pregnant women. This protocol provides a detailed overview of the steps involved in the development of a COS, to guide researchers in developing COS within their areas of specialization. COMET CORE OUTCOME SET REGISTRATION: http://www.comet-initiative.org/studies/details/939. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-3029-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-62581692018-11-29 Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol Dadouch, Rachel Faheim, Mina Juando-Prats, Clara Parsons, Janet D’Souza, Rohan Trials Study Protocol BACKGROUND: Maternal obesity is a risk factor for adverse maternal, fetal, and neonatal events. Numerous clinical trials are currently exploring the effectiveness of antenatal and peripartum interventions in improving pregnancy outcomes that can in future inform clinical practice. However, the heterogeneity in outcome reporting limits our ability to compare outcomes across studies, and there is a lack of stakeholder representation in outcome choice. A pragmatic solution to this problem is the development of a core outcome set (COS) that defines the minimum criteria for outcome reporting in clinical trials undertaken in this population, arrived at by the involvement of relevant stakeholders. METHODS: The development of a COS for studies on obesity in pregnant patients (COSSOPP) will comprise five steps. First, a systematic review of published literature will identify the long list of outcomes, their definitions and measurements if applicable, and outcome reporting quality. This will be followed by a meta-synthesis of qualitative studies with patients, and qualitative interviews in Toronto with patients, clinicians, researchers, hospital administrators, and policy-makers, to identify novel outcomes that were not obtained through systematic review. Third, the long list of outcomes will be narrowed down through online Delphi surveys involving an international group of patients and relevant stakeholders. This will be followed by a face-to-face consensus meeting with representatives of all stakeholder groups to arrive at a consensus on the final COS. Finally, in order to determine how the identified core outcomes should be measured, we will conduct another literature review and Delphi process. DISCUSSION: COSSOPP will engage patients, clinicians, researchers, and other relevant stakeholders in determining the core set of outcomes that should be reported and measured in order to harmonize outcome reporting in studies evaluating the effectiveness of antepartum and peripartum interventions in obese pregnant women. This protocol provides a detailed overview of the steps involved in the development of a COS, to guide researchers in developing COS within their areas of specialization. COMET CORE OUTCOME SET REGISTRATION: http://www.comet-initiative.org/studies/details/939. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-3029-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-27 /pmc/articles/PMC6258169/ /pubmed/30482249 http://dx.doi.org/10.1186/s13063-018-3029-1 Text en © The Author(s). 2018 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Dadouch, Rachel
Faheim, Mina
Juando-Prats, Clara
Parsons, Janet
D’Souza, Rohan
Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title_full Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title_fullStr Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title_full_unstemmed Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title_short Development of a Core Outcome Set for Studies on Obesity in Pregnant Patients (COSSOPP): a study protocol
title_sort development of a core outcome set for studies on obesity in pregnant patients (cossopp): a study protocol
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258169/
https://www.ncbi.nlm.nih.gov/pubmed/30482249
http://dx.doi.org/10.1186/s13063-018-3029-1
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