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评估英国研究志愿者对基因和临床研究的同意偏好。

Evaluating the consent preferences of UK research volunteers for genetic and clinical studies.

作者信息

Kelly Susan E, Spector Timothy D, Cherkas Lynn F, Prainsack Barbara, Harris Juliette M

机构信息

Centre for the Study of Life Sciences (Egenis), University of Exeter, Exeter, United Kingdom.

Department of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom.

出版信息

PLoS One. 2015 Mar 11;10(3):e0118027. doi: 10.1371/journal.pone.0118027. eCollection 2015.

Abstract

OBJECTIVES

To establish the views of research volunteers on the consent process; to explore their views on the consent process in different research scenarios; to inform debate on emerging models of consent for participation in research.

DESIGN, SETTING AND PARTICIPANTS: 2,308 adult volunteers from the TwinsUK Registry (www.twinsuk.ac.uk) completed an online survey about their views on the consent process for use of their DNA and medical information in research. Their views on the re-consenting process in different scenarios were assessed.

RESULTS

The majority of volunteers preferred to be informed of the identity of the main researcher of a study in which they are participating, which is contrary to current practice. Over 80% were willing to complete the consent process online instead of face to face. On the whole, respondents did not view their DNA differently from their medical information with regard to the consent process. Research participants were more willing to give broad consent to cover future research if their DNA was to be used by the original researcher than by another researcher, even if the disease under investigation varied, in contrast to the traditional 'gold standard' whereby specific consent is required for all new research projects.

DISCUSSION

In some scenarios, research participants reported that they would be comfortable with not signing a new consent form for future research uses of their data and DNA, and are comfortable with secure, online consent processes rather than traditional face-to-face consent processes. Our findings indicate that the perceived relationship between research participants and researchers plays an important role in shaping preferences regarding the consent process and suggest that this relationship is not captured by traditional consent processes. We argue that the development of new formats of consent should be informed by empirical research on volunteers' perceptions and preferences regarding the consent process.

摘要

目的

了解研究志愿者对同意程序的看法;探讨他们在不同研究场景下对同意程序的看法;为有关参与研究的新型同意模式的辩论提供信息。

设计、背景和参与者:来自双胞胎英国注册库(www.twinsuk.ac.uk)的2308名成年志愿者完成了一项关于在研究中使用其DNA和医疗信息的同意程序看法的在线调查。评估了他们在不同场景下对重新同意程序的看法。

结果

大多数志愿者希望被告知他们所参与研究的主要研究者的身份,这与当前的做法相反。超过80%的人愿意在线完成同意程序而非面对面进行。总体而言,在同意程序方面,受访者对其DNA和医疗信息的看法并无不同。与传统的“黄金标准”(即所有新研究项目都需要特定同意)相反,研究参与者更愿意在其DNA由原研究者使用而非其他研究者使用时,给予涵盖未来研究的广泛同意,即使所研究的疾病有所不同。

讨论

在某些场景下,研究参与者表示,他们对于不为未来研究使用其数据和DNA签署新的同意书感到安心,并且对安全的在线同意程序而非传统的面对面同意程序感到安心。我们的研究结果表明,研究参与者与研究者之间的感知关系在塑造对同意程序的偏好方面起着重要作用,并表明这种关系未被传统同意程序所体现。我们认为,新的同意形式的发展应以关于志愿者对同意程序的看法和偏好的实证研究为依据。

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