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为什么人们会参与医学研究?三项研究的结果

Why do people cooperate with medical research? Findings from three studies.

作者信息

Dixon-Woods Mary, Tarrant Carolyn

机构信息

University of Leicester, Leicester, United Kingdom.

出版信息

Soc Sci Med. 2009 Jun;68(12):2215-22. doi: 10.1016/j.socscimed.2009.03.034. Epub 2009 Apr 24.

Abstract

In this paper, we distinguish decisions about cooperation with medical research from decisions about research participation. We offer an empirical and theoretical exploration of why people in three different UK-based medical research projects chose to cooperate. Data analysis of the accounts of 128 participants across the three studies was based on the constant comparative method. Participants' cooperation was engaged by a perception that they would be contributing to the 'public good', but they also wanted to justify their decision as sensible and safe. Critical to their cooperation was their belief that researchers would fulfil their side of the cooperative bargain, by not exposing participants to risks of harm or exploitation. Although participants were generally unaware of the details of the regulatory regime for research, they demonstrated a generalised reliance on regulation as a feature of everyday life that would provide a safe context for cooperation. In their assessment of particular projects, participants made judgements about whether to cooperate based on more specific cues, which acted as signs to assure them that researchers shared their cooperative intentions. These cues included organisational and professional credentials, the role identities and perceived trustworthiness of those involved in recruiting to research, and visible signs of reasonable practice mandated by regulatory systems. Thus participants drew on their understandings of an institutional field that was much broader than that of research alone. We propose that the social organisation of research is fundamental to the judgements people make about cooperation with research. Cooperation may be a more useful way of thinking about how people come to engage in collaboratively oriented actions such as research participation, rather than currently dominant individualistic models. Attention to the institutional context of research is critical to understanding what makes cooperation possible, and has important implications for the design of regulatory regimes for research.

摘要

在本文中,我们区分了关于与医学研究合作的决策和关于参与研究的决策。我们对英国三个不同医学研究项目中的人们为何选择合作进行了实证和理论探索。对三项研究中128名参与者的叙述进行的数据分析基于持续比较法。参与者的合作是出于一种他们将为“公共利益”做出贡献的认知,但他们也希望将自己的决定证明为明智且安全的。对他们的合作至关重要的是他们相信研究人员会履行合作协议中的己方责任,即不会让参与者面临伤害或被剥削的风险。尽管参与者通常不了解研究监管制度的细节,但他们表现出对监管作为日常生活特征的普遍依赖,认为监管会为合作提供一个安全的环境。在评估特定项目时,参与者基于更具体的线索来判断是否合作,这些线索充当了确保他们研究人员与他们有共同合作意图的信号。这些线索包括组织和专业资质、参与研究招募人员的角色身份和感知到的可信度,以及监管系统规定的合理做法的可见迹象。因此,参与者借鉴了他们对一个比仅研究领域更广泛的制度领域的理解。我们认为研究的社会组织对于人们对与研究合作所做的判断至关重要。合作可能是一种比目前占主导地位的个人主义模式更有用的思考方式,用于理解人们如何开始参与诸如研究参与等以合作导向的行动。关注研究的制度背景对于理解合作成为可能的因素至关重要,并且对研究监管制度的设计具有重要意义。

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