دورية أكاديمية

Using healthcare systems data for outcomes in clinical trials: issues to consider at the design stage

التفاصيل البيبلوغرافية
العنوان: Using healthcare systems data for outcomes in clinical trials: issues to consider at the design stage
المؤلفون: Toader, Alice-Maria, Campbell, Marion K., Quint, Jennifer K., Robling, Michael, Sydes, Matthew R, Thorn, Joanna, Wright-Hughes, Alexandra, Yu, Ly-Mee, Abbott, Tom. E. F., Bond, Simon, Caskey, Fergus J., Clout, Madeleine, Collinson, Michelle, Copsey, Bethan, Davies, Gwyneth, Driscoll, Timothy, Gamble, Carrol, Griffin, Xavier L., Hamborg, Thomas, Harris, Jessica, Harrison, David A., Harji, Deena, Henderson, Emily J., Logan, Pip, Love, Sharon B., Magee, Laura A., O’Brien, Alastair, Pufulete, Maria, Ramnarayan, Padmanabhan, Saratzis, Athanasios, Smith, Jo, Solis-Trapala, Ivonne, Stubbs, Clive, Farrin, Amanda, Williamson, Paula
بيانات النشر: Springer Verlag
سنة النشر: 2024
المجموعة: University of Nottingham: Repository@Nottingham
مصطلحات موضوعية: Healthcare systems data, Outcomes, Data validity, Registries, Routinely collected data, Clinical trials
الوصف: Background: Healthcare system data (HSD) are increasingly used in clinical trials, augmenting or replacing traditional methods of collecting outcome data. This study, PRIMORANT, set out to identify, in the UK context, issues to be considered before the decision to use HSD for outcome data in a clinical trial is finalised, a methodological question prioritised by the clinical trials community. Methods: The PRIMORANT study had three phases. First, an initial workshop was held to scope the issues faced by trialists when considering whether to use HSDs for trial outcomes. Second, a consultation exercise was undertaken with clinical trials unit (CTU) staff, trialists, methodologists, clinicians, funding panels and data providers. Third, a final discussion workshop was held, at which the results of the consultation were fed back, case studies presented, and issues considered in small breakout groups. Results: Key topics included in the consultation process were the validity of outcome data, timeliness of data capture, internal pilots, data-sharing, practical issues, and decision-making. A majority of consultation respondents (n = 78, 95%) considered the development of guidance for trialists to be feasible. Guidance was developed following the discussion workshop, for the five broad areas of terminology, feasibility, internal pilots, onward data sharing, and data archiving. Conclusions: We provide guidance to inform decisions about whether or not to use HSDs for outcomes, and if so, to assist trialists in working with registries and other HSD providers to improve the design and delivery of trials.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: https://nottingham-repository.worktribe.com/output/30927415Test; Trials; Volume 25; Issue 1; https://nottingham-repository.worktribe.com/file/30927415/1/s13063-024-07926-zTest
DOI: 10.1186/s13063-024-07926-z
الإتاحة: https://doi.org/10.1186/s13063-024-07926-zTest
https://nottingham-repository.worktribe.com/file/30927415/1/s13063-024-07926-zTest
https://nottingham-repository.worktribe.com/output/30927415Test
حقوق: openAccess ; https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.272E22A9
قاعدة البيانات: BASE