Considerations for patient and public involvement and engagement in health research

公共卫生 公众参与 医学 心理学 护理部 公共关系 政治学
作者
Olalekan Lee Aiyegbusi,Christel McMullan,Sarah Hughes,Grace Turner,Anuradhaa Subramanian,Richard Hotham,Elin Haf Davies,Chris Frost,Yvonne Alder,Lisa Agyen,Lewis Buckland,Jennifer Camaradou,Amy Chong,Felicity Jeyes,Sumita Kumar,Karen Matthews,Patricia Moore,Jane Ormerod,Gary Price,Michael Saint-Cricq
出处
期刊:Nature Medicine [Nature Portfolio]
卷期号:29 (8): 1922-1929 被引量:35
标识
DOI:10.1038/s41591-023-02445-x
摘要

Patient and public involvement and engagement (PPIE) can provide valuable insights into the experiences of those living with and affected by a disease or health condition. Inclusive collaboration between patients, the public and researchers can lead to productive relationships, ensuring that health research addresses patient needs. Guidelines are available to support effective PPIE; however, evaluation of the impact of PPIE strategies in health research is limited. In this Review, we evaluate the impact of PPIE in the ‘Therapies for Long COVID in non-hospitalised individuals’ (TLC) Study, using a combination of group discussions and interviews with patient partners and researchers. We identify areas of good practice and reflect on areas for improvement. Using these insights and the results of a survey, we synthesize two checklists of considerations for PPIE, and we propose that research teams use these checklists to optimize the impact of PPIE for both patients and researchers in future studies. The authors generate a checklist of key considerations to guide patient and public involvement and engagement in future research, informed by lessons from the TLC study, which evaluated therapies for long COVID.

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