Consumer and Community Involvement Theme, Melbourne Academic Centre for Health, University of Melbourne, Melbourne, Victoria, Australia.
Clinical Translation Centre, Cancer Biology and Stem Cells Division and Inflammation Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Health Expect. 2024 Feb;27(1):e13968. doi: 10.1111/hex.13968.
Involving people with lived experience of health conditions and the public (consumers) in health research is supported by policy, practice and research funding schemes. However, consumer involvement programmes in discovery-based preclinical research settings are uncommon. Few formal evaluations of these programmes are reported in the literature.
This study aimed to evaluate an established patient and public involvement programme operating in a major Australian Discovery-Based Medical Research Institute (DBMRI) to inform programme development and the wider field.
A multimethods programme evaluation incorporating demographic, descriptive and qualitative data obtained through consumer/researcher co-developed online surveys and semistructured virtual interviews. Programme participants (n = 111) were invited to complete an online survey seeking feedback on their experience of involvement, programme processes and perceived impacts. A purposive sample of 25 participants was interviewed. Descriptive data were analysed using explanatory statistics and qualitative data from surveys and interviews were thematically analysed.
This consumer involvement programme was found to be useful and meaningful for most participants, with specific examples of perceived added value. Consumers most commonly engaged with researchers to inform research development, prepare funding applications or strengthen lay communication of science. Genuine consumer-researcher interactions, relationship development and mutual respect were key elements in a positive experience for participants. Opportunities to 'give back', to learn and to ground research in lived experience were identified programme strengths and benefits. Developing researcher training in how to work with consumers, increasing the diversity of the consumer group membership and expanding the range of consumer activities were identified opportunities for improvement. Organisational support and adequate programme resourcing were identified as key enablers.
Discovery-based preclinical research is often viewed as being distant from clinical application; therefore, consumer involvement may be considered less relevant. However this study identified value in bringing a strong consumer voice to the discovery-based research process through a coordinated, organisation-wide approach with the potential for application in similar preclinical research settings.
Four consumer partners from the DBMRI Consumer Advisory Panel were actively engaged in developing this programme evaluation. Specifically, these consumer partners co-developed and pilot-tested surveys and interview guides, reviewed and commented on project data analysis and reporting and also contributed as co-authors by editing the manuscript.
将有健康状况生活经历的人和公众(消费者)纳入健康研究,这一做法受到政策、实践和研究资助计划的支持。然而,在基于发现的临床前研究环境中,消费者参与项目并不常见。文献中很少有关于这些项目的正式评估。
本研究旨在评估在澳大利亚一家主要的基于发现的医学研究机构(DBMRI)中运作的成熟患者和公众参与计划,为项目发展和更广泛的领域提供信息。
一项多方法的计划评估,包括通过消费者/研究人员共同开发的在线调查和半结构化虚拟访谈获得的人口统计学、描述性和定性数据。计划参与者(n=111)受邀完成在线调查,以反馈他们的参与体验、计划流程和感知影响。对 25 名参与者进行了有针对性的访谈。使用解释性统计方法分析描述性数据,对调查和访谈的定性数据进行主题分析。
该消费者参与计划被大多数参与者认为是有用且有意义的,具体例子包括感知到的附加价值。消费者最常与研究人员合作,以告知研究进展、准备资助申请或加强科学的通俗传播。真正的消费者-研究人员之间的互动、关系发展和相互尊重是参与者获得积极体验的关键要素。参与者认为,有机会“回馈”、学习和将研究扎根于生活经历是该计划的优势和收益。发展研究人员与消费者合作的能力、增加消费者群体成员的多样性以及扩大消费者活动的范围被认为是改进的机会。组织支持和充足的计划资源被确定为关键的促成因素。
基于发现的临床前研究通常被认为与临床应用相距甚远;因此,消费者参与可能被认为不太相关。然而,本研究通过协调一致的、全组织范围的方法,在发现的基础上识别了研究过程中引入强大的消费者声音的价值,该方法具有在类似的临床前研究环境中应用的潜力。
来自 DBMRI 消费者咨询小组的四名消费者合作伙伴积极参与了该计划评估的制定。具体来说,这些消费者合作伙伴共同开发和试点测试了调查和访谈指南,审查和评论了项目数据分析和报告,并通过编辑手稿作为共同作者做出了贡献。