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Rethinking the relationship between science and society: Has there been a shift in attitudes to Patient and Public Involvement and Public Engagement in Science in the United Kingdom?

机译:重新思考科学与社会之间的关系:英国对患者和公众参与以及公众参与科学的态度是否发生了转变?

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摘要

BACKGROUND: The policy imperative to engage the public and patients in research can be seen as part of a wider shift in the research environment. This study addresses the question: Has there been a shift in attitudes to Patient and Public Involvement (PPI) and Public Engagement in Science (PES) amongst researchers? METHODS: Attitudes to PPI and PES within a cluster of three NIHR supported Biomedical Research Centres were explored through in-depth interviews with 19 researchers. RESULTS: Participants distinguished PPI (as an activity involving patients and carers in research projects and programmes) from PES (as an activity that aims to communicate research findings to the public, engage the public with broader issues of science policy or promote a greater understanding of the role of science in society). While participants demonstrated a range of attitudes to these practices, they shared a resistance to sharing power and control of the research process with the public and patients.\udCONCLUSION: While researchers were prepared to engage with the public and patients and listed the advantages of engagement, the study revealed few differences in their underlying attitudes towards the role of society in science (and science in society) to those reported in previous studies. To the participants science remains the preserve of scientists, with patients and the public invited to 'tinker at the edges'.
机译:背景:促使公众和患者参与研究的政策必须被视为研究环境更广泛转变的一部分。这项研究解决了一个问题:研究人员对患者和公众参与(PPI)和公众参与科学(PES)的态度是否有所转变?方法:通过与19名研究人员的深入访谈,探讨了由三个NIHR支持的生物医学研究中心组成的集群中对PPI和PES的态度。结果:参与者将PPI与PES区别开来(PPI是一项涉及患者和护理人员参与研究项目和计划的活动),PPI是一项旨在向公众传达研究结果,使公众参与更广泛的科学政策问题或增进对科学在社会中的作用)。尽管参与者对这些做法表现出了各种各样的态度,但他们与公众和患者分享了反对共享权力和控制研究过程的阻力。\ ud结论:虽然研究人员准备与公众和患者互动,但列出了参与的优势,该研究表明,他们对科学在社会(以及科学在社会)中的作用的基本态度与以前的研究几乎没有区别。对于参与者来说,科学仍然是科学家的保护之本,患者和公众都被邀请参加“边缘研究”。

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