社区参与基因研究:魁北克CARTaGENE项目第一次公众咨询的结果。

Béatrice Godard, Jennifer Marshall, Claude Laberge
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引用次数: 103

摘要

目的:本文介绍了魁北克CARTaGENE项目建立大规模遗传数据库的第一次公众咨询的结果。政府已进行谘询,以评估公众是否接受这项计划。研究人员的方法的一个组成部分是建立与公众的对话。方法:两个独立专家组进行了定性和定量研究,测量了遗传学知识和兴趣、参与CARTaGENE的动机和障碍以及对沟通工具的理解和评估。结果:CARTaGENE被认为对更大的人群有希望。然而,在定性和定量研究中报告的是对保密和尊重个人、透明度、捐助者的反馈权和治理的关注。参与的条件是对这些关切作出反应和更多地传播信息。结论:社区参与基因研究需要有针对性的交流,信息和交流的比例适当,并根据不同的社会阶层考虑个人的“价值观和个人利益”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Community engagement in genetic research: results of the first public consultation for the Quebec CARTaGENE project.

Objective: This paper presents the results of the first public consultation for the creation of a large-scale genetic database, the Quebec CARTaGENE project. A consultation has been undertaken in order to gauge whether the general public is receptive to the project. An integral part of the approach of the researchers is to establish a dialogue with the public.

Methods: Two independent expert groups have carried out qualitative and quantitative studies measuring knowledge of and interest in genetics, incentives and obstacles to CARTaGENE participation and comprehension and evaluation of the communication tools.

Results: CARTaGENE is seen to hold promise for the greater population. However, reported across qualitative and quantitative studies is the concern for confidentiality and respect for the individual, transparency, the donor's right to feedback and governance. Participation would be conditional on a response to those concerns and a greater dissemination of information.

Conclusion: Community engagement in genetic research requires targeted communications, with an appropriate proportioning of information and communication, and a consideration of the 'values and personal interests' of individuals according to different societal segments.

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