Bevan Charlotte, Alderdice Fiona, Darby Sally, Gilzean-Hughes Serena, McLeish Jenny, Mulla Sumayya, Plachcinski Rachel, Wilkinson Sophia, Williams Harriet, Rowe Rachel
Patient and Public Involvement and Engagement (PPIE) co-lead, NIHR Policy Research Unit in Maternal and Neonatal Health and Care (PRU-MNHC), National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Old Road Campus, Oxford, OX3 7LF, UK.
Co-Director, National Perinatal Epidemiology Unit, Nuffield Department of Population Health, NIHR PRU-MNHC, University of Oxford, Oxford, UK.
Res Involv Engagem. 2024 Jul 4;10(1):71. doi: 10.1186/s40900-024-00601-2.
Policy research aims to provide evidence to inform government policy decisions about health and social care. Engaging and involving the public and patients in this work is widely recognised as essential. Research funders prioritise equality, diversity and inclusion (EDI) in patient and public involvement and engagement (PPIE), but people who are most likely to experience poor outcomes are also those least likely to be involved in research. This paper describes our experience of setting out to understand how to overcome barriers to EDI in PPIE in the research carried out by the National Institute for Health and Care Research (NIHR) Policy Research Unit in Maternal and Neonatal Health and Care (PRU-MNHC), in a PPIE consultation project we called The Listening Series.
We convened five video-recorded online discussion groups involving 20 individuals advocating for groups who are under-represented in our research. Those taking part included people working with Black and Asian women and families, young parents, those from socially deprived backgrounds, and women and families with physical and learning disabilities. Discussions focussed on practical solutions to addressing challenges to people being excluded, and how to improve EDI in our research.
Five key themes were identified: 'build trust'; 'involve us from the beginning'; 'show us impact'; 'use clear, appropriate and inclusive communication'; and 'imagine life in our shoes'. We used the learning to create a guidance document for researchers and an accompanying 15-minute film. We also took practical steps to embed the learning strategically by expanding our Task Group for PPIE in the PRU-MNHC to include four Listening Series invitees with a remit to champion EDI in our research and ensure that it is embedded in our PPIE activities. We continue to reflect on and work to address the associated challenges.
The Listening Series helped us rethink our processes for inclusion to go beyond traditional methods of involvement and engagement. The themes identified pose challenges that require time, resource and empathic engagement from researchers to be meaningfully resolved. This has implications for policy makers and research funders who need to consider this in their processes.
政策研究旨在提供证据,为政府有关健康和社会护理的政策决策提供参考。让公众和患者参与这项工作被广泛认为至关重要。研究资助者将平等、多样性和包容性(EDI)作为患者和公众参与及介入(PPIE)工作的重点,但最有可能经历不良后果的人群也是最不可能参与研究的人群。本文描述了我们在国家卫生与保健研究机构(NIHR)孕产妇和新生儿健康与保健政策研究组(PRU-MNHC)开展的一项PPIE咨询项目“倾听系列”中,为了解如何克服PPIE中EDI障碍所做的经历。
我们召集了五个线上视频讨论组,共有20人参与,这些人代表了在我们研究中代表性不足的群体。参与者包括与黑人及亚裔女性和家庭、年轻父母、社会贫困背景人群以及有身体和学习障碍的女性和家庭打交道的人员。讨论聚焦于应对人们被排斥所面临挑战的实际解决方案,以及如何在我们的研究中改善EDI。
确定了五个关键主题:“建立信任”;“从一开始就让我们参与”;“向我们展示影响”;“使用清晰、恰当且包容的沟通方式”;“设身处地为我们着想”。我们利用这些经验为研究人员创建了一份指导文件以及一部15分钟的配套影片。我们还采取了实际措施,通过将PRU-MNHC的PPIE任务组扩大,纳入四位“倾听系列”受邀者,从战略上融入所学内容,其职责是在我们的研究中倡导EDI,并确保其融入我们的PPIE活动。我们继续反思并努力应对相关挑战。
“倾听系列”帮助我们重新思考纳入流程,超越传统的参与和介入方法。所确定的主题带来了挑战,需要研究人员投入时间、资源并以同理心参与才能得到有意义的解决。这对政策制定者和研究资助者有启示意义,他们需要在其流程中考虑这一点。