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Relevant Information and Informed Consent in Research: In Defense of the Subjective Standard of Disclosure

机译:相关信息和研究中的知情同意:为公开的主观标准辩护

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摘要

In this article, we seek to contribute to the debate on the requirement of disclosure in the context of informed consent for research. We defend the subjective standard of disclosure and describe ways to implement this standard in research practice. We claim that the researcher should make an effort to find out what kinds of information are likely to be relevant for those consenting to research. This invites researchers to take empirical survey information seriously, attempt to understand the cultural context, talk to patients to be better able to understand what can be potentially different concerns and interests prevalent in the target population. The subjective standard of disclosure should be seen as a moral ideal that perhaps can never be perfectly implemented but still can and should be used as a normative ideal guiding research practice. In the light of these discussions, we call for more empirical research on what considerations are likely to be perceived as relevant by potential research participants recruited from different socio-economic and cultural groups.
机译:在本文中,我们力求为研究知情同意的背景下有关公开要求的辩论做出贡献。我们捍卫公开的主观标准,并描述在研究实践中实施该标准的方式。我们认为研究人员应该努力找出哪些信息可能与那些同意研究的人有关。这邀请研究人员认真对待经验调查信息,尝试了解文化背景,与患者交谈,以更好地了解目标人群中普遍存在的潜在不同关注和兴趣。公开的主观标准应被视为一种道德理想,也许永远无法完美实现,但仍可以并且应该被用作指导研究实践的规范理想。根据这些讨论,我们呼吁对来自不同社会经济和文化群体的潜在研究参与者认为哪些考虑因素可能具有相关性进行更多的实证研究。

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