دورية أكاديمية

Vitiligo International Task force for an Agreed List of core data (VITAL):study protocol of a vitiligo core outcome set (COS) and contextual factors for clinical trials, registries, and clinical practice

التفاصيل البيبلوغرافية
العنوان: Vitiligo International Task force for an Agreed List of core data (VITAL):study protocol of a vitiligo core outcome set (COS) and contextual factors for clinical trials, registries, and clinical practice
المؤلفون: van Geel, Nanja, Hamzavi, Iltefat H., Pandya, Amit G., Wolkerstorfer, Albert, Seneschal, Julien, Garg, Amit, Spuls, Phyllis, Terwee, Caroline B., Mallett, Sue, Speeckaert, Reinhart, Meurant, Jean Marie, Eleftheriadou, Viktoria, Ezzedine, Khaled
المصدر: van Geel , N , Hamzavi , I H , Pandya , A G , Wolkerstorfer , A , Seneschal , J , Garg , A , Spuls , P , Terwee , C B , Mallett , S , Speeckaert , R , Meurant , J M , Eleftheriadou , V & Ezzedine , K 2022 , ' Vitiligo International Task force for an Agreed List of core data (VITAL) : study protocol of a vitiligo core outcome set (COS) and contextual factors for clinical trials, registries, and clinical practice ' , Trials , vol. 23 , no. ....
سنة النشر: 2022
الوصف: Background: There is a lack of consensus related to the collection of standardized data for individuals with vitiligo enrolled in clinical trials and registries as well as those seen in clinical practice which causes difficulty in accurately interpreting, comparing, and pooling of data. Several years ago, efforts to initiate work on developing core outcome sets were performed and a consensus was reached in 2015 on the first core domain set for vitiligo clinical trials. Methods/design: This project aims to further develop a core outcome set for vitiligo clinical trials as well as create internationally agreed-upon core outcome sets for registries and clinical practice. These core outcome sets will include a core domain set and a core measurement instruments set and will be supplemented by contextual factors, including baseline and treatment-related characteristics. In a preparatory exercise, the 2015 core domain set will be re-evaluated and will serve as the basis for the list of outcome domains used to initiate the consensus process. This project will consist of two parts. Part 1 will focus on the selection of a core domain set, or “what to measure” and contextual factors, for each setting based on electronic surveys (e-Delphi technique) and a conclusive consensus meeting by a large group of international stakeholders. Part 2 will include selection of core measurement instruments, or “how to measure,” and measurement details (e.g., scale and timing) for the core domain sets and contextual factors agreed upon in part 1. Part 2 will be based on consensus meetings with stakeholders involved in part 1 and will be guided by C3 (CHORD-COUSIN Collaboration), Harmonising Outcome Measures for Eczema (HOME), COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN), and Outcome Measures in Rheumatology (OMERACT) recommendations including information on measurement properties of available instruments (systematic review and expert/patient opinion). At the end of part 2, all stakeholders involved ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: https://research.vumc.nl/en/publications/4babe9fc-462a-4b3c-875f-02e7e1a82b83Test
DOI: 10.1186/s13063-022-06497-1
الإتاحة: https://doi.org/10.1186/s13063-022-06497-1Test
https://research.vumc.nl/en/publications/4babe9fc-462a-4b3c-875f-02e7e1a82b83Test
http://www.scopus.com/inward/record.url?scp=85135014315&partnerID=8YFLogxKTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.8E2EC5B4
قاعدة البيانات: BASE