Tripp Laura, Richards Dawn P, Daly-Cyr Jennifer, Lane Therese, Linkiewich Delane, Begley Kimberly N, Buckley Norman, Hudspith Maria, Poulin Patricia, Abelson Julia
Public and Patient Engagement Collaborative, McMaster University, Hamilton, ON, Canada.
Chronic Pain Network, McMaster University, Hamilton, ON, Canada.
Res Involv Engagem. 2023 Aug 30;9(1):73. doi: 10.1186/s40900-023-00491-w.
The Chronic Pain Network (CPN) is a pan-Canadian research network focused on innovating and improving the quality and delivery of pain prevention, assessment, management and research for all Canadians. An important focus of the CPN is to work in collaboration with patient partners. Patient partners, researchers and clinicians work together in all aspects of the research network including on funded research projects and in the governance of the Network. Given this focus, the CPN identified the importance of evaluating their patient engagement work to understand its functioning and impact.
The objective of this exploratory evaluation case study was to understand the impacts of patient engagement on the CPN. The CPN worked with an external evaluation team which established an arms-length approach to the evaluation. Interviews were conducted with CPN members, including patient partners, leadership, funded researchers and committee co-chairs, at three discrete time points to trace the evolution of the patient engagement program within the Network. Key Network documents were also collected and reviewed. Data were analyzed following each set of interviews using content analysis guided by the principles of constant comparison and qualitative description. A final round of analysis was conducted using the Engage with Impact Toolkit, an impact measurement framework, to identify impacts of engagement.
Impacts of patient engagement were identified at the individual, network, funded research project and research community levels. These impacts were observed in the following areas: (1) building community; (2) developing knowledge, skills and resources; (3) increasing confidence; (4) influencing priorities and decisions; (5) enabling additional opportunities; (6) promoting culture change; and, (7) coping with experiences of living with chronic pain.
While not without challenges, the patient engagement efforts of the CPN demonstrates the impact engaging patient partners can have on a national research network and related policy activities. Understanding the approaches to, and impacts of, patient engagement on health research networks can illuminate the value of having patient partners engaged in all aspects of a research network and should serve as encouragement to others who look to take on similar work.
慢性疼痛网络(CPN)是一个泛加拿大研究网络,专注于为所有加拿大人创新并提高疼痛预防、评估、管理及研究的质量与实施。CPN的一个重要重点是与患者伙伴合作。患者伙伴、研究人员和临床医生在研究网络的各个方面共同合作,包括在获得资助的研究项目以及网络治理方面。鉴于此重点,CPN认识到评估其患者参与工作以了解其运作和影响的重要性。
本探索性评估案例研究的目的是了解患者参与对CPN的影响。CPN与一个外部评估团队合作,该团队采用独立的评估方法。在三个不同时间点对CPN成员进行访谈,包括患者伙伴、领导层、获得资助的研究人员和委员会联合主席,以追踪网络内患者参与计划的演变。还收集并审查了关键的网络文件。在每组访谈后,使用以持续比较和定性描述原则为指导的内容分析法对数据进行分析。最后一轮分析使用“参与产生影响工具包”(一种影响衡量框架)来确定参与的影响。
在个人、网络、获得资助的研究项目和研究社区层面都发现了患者参与的影响。这些影响体现在以下方面:(1)建立社区;(2)发展知识、技能和资源;(3)增强信心;(4)影响优先事项和决策;(5)创造更多机会;(6)促进文化变革;以及(7)应对慢性疼痛的生活经历。
虽然并非没有挑战,但CPN的患者参与工作证明了让患者伙伴参与对国家研究网络及相关政策活动所能产生的影响。了解患者参与健康研究网络的方法和影响,可以阐明让患者伙伴参与研究网络各个方面的价值,并应激励其他希望开展类似工作的人。