Warwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.
School of Psychological, Social and Behavioural Sciences, Coventry University, Coventry, CV1 5FB, UK.
Prim Health Care Res Dev. 2021 Nov 19;22:e72. doi: 10.1017/S1463423621000670.
Patient and public involvement (PPI) plays a crucial role in ensuring research is carried out in conjunction with the people that it will impact upon. In this article, we present our experiences and reflections from working collaboratively with patients and public through the lifetime of an National Institute for Health Research (NIHR) programme grant; the Chronic Headache Education and Self-management Study (CHESS) which took place between 2015 and 2020.
We worked closely with three leading UK migraine charities and a lay advisory group throughout the programme. We followed NIHR standards and used the Guidance for Reporting Involvement of Patients and the Public checklist. We consulted our PPI contacts using a variety of methods depending on the phase of the study and the nature of the request. This included emails, discussions, and face-to-face contact.PPI members contributed throughout the study in the programme development, in the grant application, ethics documentation, and trial oversight. During the feasibility study; in supporting the development of a classification interview for chronic headache by participating in a headache classification conference, assessing the relevance, and acceptability of patient-reported outcome measures by helping to analyse cognitive interview data, and testing the smartphone application making suggestions on how best to present the summary of data collected for participants. Due to PPI contribution, the content and duration of the study intervention were adapted and a Delphi study with consensus meeting developed a core outcome set for migraine studies.
The involvement of the public and patients in CHESS has allowed us to shape its overall design, intervention development, and establish a core outcome set for future migraine studies. We have reflected on many learning points for the future application of PPI.
患者和公众参与(PPI)在确保研究与受其影响的人群共同进行方面发挥着至关重要的作用。在本文中,我们介绍了在英国国家卫生研究院(NIHR)计划资助的整个生命周期中,通过与患者和公众合作,从慢性头痛教育和自我管理研究(CHESS)中获得的经验和体会。该研究于 2015 年至 2020 年进行。
PPI 在 CHESS 中的作用:在整个项目中,我们与三家领先的英国偏头痛慈善机构和一个外行顾问小组密切合作。我们遵循了 NIHR 的标准,并使用了《患者和公众参与报告指南》清单。根据研究阶段和请求的性质,我们使用各种方法与我们的 PPI 联系人进行咨询。这些方法包括电子邮件、讨论和面对面的交流。PPI 成员在整个研究过程中都有贡献,包括在项目开发、资助申请、伦理文件和试验监督方面。在可行性研究期间,通过参与头痛分类会议、帮助分析认知访谈数据来评估患者报告结局测量的相关性和可接受性、测试智能手机应用程序并提出如何最好地展示参与者收集的数据摘要的建议,他们为慢性头痛的分类访谈的开发提供了支持。由于 PPI 的贡献,研究干预的内容和持续时间得到了调整,并通过德尔菲研究和共识会议为偏头痛研究制定了核心结局集。
CHESS 中的公众和患者的参与使我们能够塑造其整体设计、干预措施的开发,并为未来的偏头痛研究建立了核心结局集。我们对未来 PPI 的应用有许多反思和学习点。