Abstract
Abstract
Background
Research study participants can stop taking part early, in various circumstances. Sometimes this experience can be stressful. Providing participants with the information they want or need when they stop could improve participants’ experiences, and may benefit individual studies’ objectives and research in general. A group of public contributors and researchers at the Clinical Trials Research Unit, University of Leeds, aimed to develop a communication template and researcher guidance. This would address how to provide information sensitively around the time when participants stop or significantly reduce their level of participation.
Methods
The project lead used scoping review methods to identify relevant prior evidence and derive a list of potential information topics to communicate to participants who stop taking part. The topic list was reviewed by research professionals and public contributors before finalisation. Further public contributors were identified from a range of networks. The contributors formed a ‘development group’, to work on the detail of the planned resources, and a larger ‘review group’ to review the draft output before finalisation. The involvement was planned so that the development group could shape the direction and pace of the work.
Results
The literature review identified 413 relevant reports, resulting in 94 information topics. The review suggested that this issue has not been well explored previously. Some evidence suggested early-stopping participants are sometimes excluded from important communications (such as study results) without clear justification. The development group agreed early to focus on guidance with reusable examples rather than a template. We took time to explore different perspectives and made decisions by informal consensus. Review group feedback was broadly positive but highlighted the need to improve resource navigability, leading to its final online form.
Conclusions
We co-developed a resource to provide support to research participants who stop taking part. A strength of this work is that several of the public contributors have direct lived experience of stopping research participation. We encourage others to review the resource and consider how they support these participants in their studies. Our work highlights the value of researchers and participants working together, including on complex and ethically challenging topics.
Funder
National Institute for Health and Care Research
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. Cox K, Wilson E, Arthur A, Elkan R, Armstrong S. A randomised controlled trial of nurse-managed trial conclusion following early phase cancer trial participation. Br J Cancer. 2005;93(1):41–5. https://doi.org/10.1038/SJ.BJC.6602675.
2. Ulrich CM, Knafl K, Foxwell AM, et al. Experiences of patients after withdrawal from cancer clinical trials. JAMA Netw Open. 2021;4(8):e2120052. https://doi.org/10.1001/jamanetworkopen.2021.20052.
3. National Institute for Health and Care Research. 2022/23 Participant in Research Experience Survey (PRES) executive summary. https://www.nihr.ac.uk/documents/202223-pres-executive-summary/34466. Accessed 29 Nov 2023.
4. The PeRSEVERE project (PRincipleS for handling end-of-participation EVEnts in clinical trials REsearch. https://persevereprinciples.org/. Accessed 29 Nov 2023.
5. PeRSEVERE principle O2: participants decide how their participation changes. https://persevereprinciples.org/principle-o2-participants-decide-how-their-participation-changes/. Accessed 29 Nov 2023.
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