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公众参与个性化健康研究和生物库的意愿:一项大规模的瑞士调查。

Public willingness to participate in personalized health research and biobanking: A large-scale Swiss survey.

机构信息

Health Ethics and Policy Lab, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.

Institute for Social and Preventive Medicine, University of Bern, Bern, Switzerland.

出版信息

PLoS One. 2021 Apr 1;16(4):e0249141. doi: 10.1371/journal.pone.0249141. eCollection 2021.

Abstract

This paper reports survey findings on the Swiss public's willingness, attitudes, and concerns regarding personalized health research participation by providing health information and biological material. The survey reached a sample of 15,106 Swiss residents, from which we received 5,156 responses (34.1% response rate). The majority of respondents were aware of research using human biological samples (71.0%) and held a positive opinion towards this type of research (62.4%). Of all respondents, 53.6% indicated that they would be willing to participate in a personalized health research project. Willingness to participate was higher in younger, higher educated, non-religious respondents with a background in the health sector. Respondents were more willing to provide 'traditional' types of health data, such as health questionnaires, blood or biological samples, as opposed to social media or app-related data. All respondents valued the return of individual research results, including risk for diseases for which no treatment is available. Our findings highlight that alongside general positive attitudes towards personalized health research using data and samples, respondents have concerns about data privacy and re-use. Concerns included potential discrimination, confidentiality breaches, and misuse of data for commercial or marketing purposes. The findings of this large-scale survey can inform Swiss research institutions and assist policymakers with adjusting practices and developing policies to better meet the needs and preferences of the public. Efforts in this direction could focus on research initiatives engaging in transparent communication, education, and engagement activities, to increase public understanding and insight into data sharing activities, and ultimately strengthen personalized health research efforts.

摘要

本论文报告了一项关于瑞士公众对参与提供健康信息和生物材料的个性化健康研究的意愿、态度和关注点的调查结果。该调查覆盖了 15106 名瑞士居民,共收到 5156 份回复(34.1%的回复率)。大多数受访者了解使用人类生物样本的研究(71.0%),并对这类研究持积极态度(62.4%)。在所有受访者中,53.6%表示愿意参与个性化健康研究项目。在年龄较小、受教育程度较高、无宗教信仰且在医疗保健领域有背景的受访者中,参与意愿更高。受访者更愿意提供“传统”类型的健康数据,如健康问卷、血液或生物样本,而不是社交媒体或应用程序相关的数据。所有受访者都重视个人研究结果的回报,包括针对尚无治疗方法的疾病的风险。我们的研究结果表明,除了对使用数据和样本的个性化健康研究普遍持积极态度外,受访者还对数据隐私和再利用表示担忧。担忧包括潜在的歧视、机密性泄露以及出于商业或营销目的滥用数据。这项大规模调查的结果可以为瑞士研究机构提供信息,并帮助政策制定者调整实践和制定政策,以更好地满足公众的需求和偏好。为此,可集中开展一些宣传活动,以提高公众对数据共享活动的理解和认识,并最终加强个性化健康研究工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87f8/8016315/ccc3f2d90003/pone.0249141.g001.jpg

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