设计一种灵活和包容的方法,让公众和社区参与对无家可归者或弱势住房者的研究:来自“我不仅仅是……”项目的批判性反思

IF 3.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Mel Hughes, Kate Jupp, Cathy Beresford, Jim Robertson, Annabel Wathen, Tanya Bailey, Siobhan Lennon-Patience, Mike Graham, Deano Pickering, Helena Posnett
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引用次数: 0

摘要

无家可归者或弱势住房者面临严重的卫生不平等,但很少作为参与者、公共贡献者或共同研究人员参与卫生和社会保健研究。“I Am More Than…”项目旨在通过与社区组织和有无家可归或脆弱住房生活经历的个人合作,解决这种缺乏包容性的问题。目的为公众和社区参与研究(有时称为公众和患者参与或PPI)共同设计一种灵活和包容的方法。方法该项目借鉴了一系列合作生产和参与式研究战略,并听取了各利益攸关方的意见,以确定和解决参与的促进因素和障碍。具有无家可归或弱势住房生活经验的社区研究人员在项目的所有阶段都处于中心地位,包括通过对话、访谈、创造性产出和利益相关者活动共同设计吸引人们的策略。我们确定了公众和社区参与研究的核心原则。包括需要:发展关系第一,任务第二;深入了解社区及其优先事项;利用生活经验专长;然而,有人可能会选择分享它;以信任的步伐前行;并与融入社区的志愿组织和社区部门组织合作。为公众和社区参与研究制定灵活和包容的方法需要从交易方法转向关系方法。该项目展示了建立信任、合作、灵活和响应人们日常现实的重要性,以实现真正的包容。这是一个由一所大学、一个综合护理系统、两个社区组织和无家可归者或弱势住房者共同制作的项目。有生活经验的个人作为社区研究人员参与其中,塑造设计、方法和结果。他们的贡献在整个论文中都有详细介绍,这篇论文是由项目组成员共同撰写的,其中包括来自两个社区组织的工作人员和一个社区研究员。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Designing a Flexible and Inclusive Approach for Public and Community Involvement in Research With People Who Are Homeless or Vulnerably Housed: Critical Reflections From the I Am More Than… Project

Background

People who are homeless or vulnerably housed face significant health inequities and yet are rarely involved in health and social care research as participants, public contributors or co-researchers. The I Am More Than… project was developed to address this lack of inclusion by working in partnership with community organisations and individuals with lived experiences of being homeless or vulnerably housed.

Objective

To co-design a flexible and inclusive approach for public and community involvement in research (sometimes referred to as public and patient involvement or PPI).

Methods

The project drew on a range of co-production and participatory research strategies, with input from various stakeholders, to identify and address enablers and barriers to participation. Community researchers with lived experience of homelessness or being vulnerably housed were central to all stages of the project, including the co-design of strategies to engage people through conversations, interviews, creative outputs and stakeholder events.

Findings

We identified core principles for inclusive public and community involvement in research. including the need to: develop relationships first and tasks second; gain a deep understanding of communities and their priorities; harness lived experience expertise; however someone may choose to share it; go at the pace of trust; and work in partnership with voluntary and community sector organisations who are embedded in their communities.

Conclusion

Developing a flexible and inclusive approach to public and community involvement in research required shifting from a transactional approach to a relational approach. The project demonstrated the importance of building trust, working in partnership and being flexible and responsive to people's everyday realities for genuine inclusion to be achieved.

Patient or Public Contribution

This is a co-produced project between a university, an integrated care system, two community organisations and people experiencing homelessness or being vulnerably housed. Individuals with lived experience participated as community researchers, shaping the design, methods and outcomes. Their contributions are detailed throughout the paper, which is co-authored by members of the project team, including staff from two community organisations and one community researcher.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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