关于医学研究中知识转化和社区参与的态度和看法:spect定性研究。

IF 3.2 2区 医学 Q1 HEALTH POLICY & SERVICES
Bogna A Drozdowska, Nora Cristall, Joachim Fladt, Tanaporn Jaroenngarmsamer, Arshia Sehgal, Rosalie McDonough, Mayank Goyal, Aravind Ganesh
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引用次数: 0

摘要

背景:医学研究界广泛赞同确保研究成果对知识用户具有相关性和可及性的重要性,以及让知识用户参与实现这些目标的研究的价值。然而,这些原则似乎在实际的医学研究实践中得到了有限的反映。为了更好地理解这种不协调,我们对主要利益相关者在弥合知识到行动的差距以及患者和公众参与方面的观点进行了定性调查。方法:研究人员、捐赠者、患者和公众对医学研究的资助和行为的优先事项和期望(spect)定性研究涉及对四个利益相关者群体代表的深入、半结构化访谈。除其他主题外,与会者被要求讨论与将医学研究知识转化为行动(知识转化)有关的问题,包括在研究过程中作为这一进程成功的先决条件的患者和公众参与。我们采用解释性扎根理论方法分析了收集到的数据。一旦专题饱和就结束数据收集。结果:共完成和分析了41次访谈(10名患者、10名公众、11名研究人员和10名资助者)。许多与会者表示,他们相信让患者参与研究过程的重要性,以及确保研究结果超越学术界。然而,在实践中实施这些价值观面临着多重挑战和障碍,包括:研究人员在促进与社区成员建立伙伴关系方面的知识和工具有限;更广泛的公众无法获得研究成果;考虑到所需的时间、精力和知识,公众没有足够的能力吸收研究结果并为正在进行的研究做出贡献。总的来说,访谈表明了研究和非专业群体之间的持续脱节,每个利益相关者群体都有责任改进当前的范式。结论:沟通、知识和相关能力方面的现有差距正在加剧研究与非专业社区之间的脱节。成功地将研究知识转化为行动,需要多个利益相关者团体在外部资源的支持下共同努力,以确保必要的培训、专业知识和可信的传播平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Attitudes and perceptions regarding knowledge translation and community engagement in medical research: the PERSPECT qualitative study.

Attitudes and perceptions regarding knowledge translation and community engagement in medical research: the PERSPECT qualitative study.

Attitudes and perceptions regarding knowledge translation and community engagement in medical research: the PERSPECT qualitative study.

Background: The medical research community widely endorses the importance of ensuring that research outputs are relevant and accessible to knowledge users, as well as the value of engaging the latter in the conduct of research to achieve these goals. However, it appears these principles are reflected in actual medical research practices to a limited extent. To better understand this dissonance, we conducted a qualitative investigation into the perspectives of key stakeholders on bridging the knowledge-to-action gap and patient and public engagement.

Methods: The Priorities and Expectations of Researchers, Donors, Patients and the Public Regarding the Funding and Conduct of Medical Research (PERSPECT) qualitative study involved in-depth, semi-structured interviews with representatives of four stakeholder groups. Among other topics, participants were asked to discuss issues related to moving medical research knowledge into action (knowledge translation), including patient and public engagement during the research journey as a prerequisite to the success of this process. We analysed collected data employing an interpretative grounded theory approach. Data collection was ended once thematic saturation had been attained.

Results: A total of 41 interviews were completed and analysed (with 10 patients, 10 members of the general public, 11 researchers and 10 funders). Many participants expressed a belief in the importance of engaging patients in the research process, as well as ensuring that study findings reach beyond academic communities. However, multiple challenges and barriers were identified to implementing these values in practice, including: researchers having limited knowledge and tools to foster partnerships with community members; research outputs being inaccessible to the wider public; and the public having insufficient capacity - in view of the required time, effort and knowledge - to assimilate findings and contribute to ongoing research. Cumulatively, interviews indicated a continuing disconnect between research and lay communities, where each stakeholder group holds some responsibility for improving the current paradigm.

Conclusions: Existing gaps in communication, knowledge and relevant competencies are fuelling a disconnect between research and lay communities. Successfully moving research knowledge into action requires joint efforts of multiple stakeholder groups with support from external resources to ensure necessary training, expertise and credible dissemination platforms.

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来源期刊
Health Research Policy and Systems
Health Research Policy and Systems HEALTH POLICY & SERVICES-
CiteScore
7.50
自引率
7.50%
发文量
124
审稿时长
27 weeks
期刊介绍: Health Research Policy and Systems is an Open Access, peer-reviewed, online journal that aims to provide a platform for the global research community to share their views, findings, insights and successes. Health Research Policy and Systems considers manuscripts that investigate the role of evidence-based health policy and health research systems in ensuring the efficient utilization and application of knowledge to improve health and health equity, especially in developing countries. Research is the foundation for improvements in public health. The problem is that people involved in different areas of research, together with managers and administrators in charge of research entities, do not communicate sufficiently with each other.
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