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3
Racial and ethnic differences in older adults' willingness to be contacted about Alzheimer's disease research participation.老年人在参与阿尔茨海默病研究方面愿意被联系的种族和民族差异。
Alzheimers Dement (N Y). 2020 May 8;6(1):e12023. doi: 10.1002/trc2.12023. eCollection 2020.
4
Audience segmentation as a strategy for enhancing the use of research registries for recruiting patients into clinical trials.受众细分作为一种策略,用于加强利用研究注册库招募患者参与临床试验。
Contemp Clin Trials Commun. 2019 Dec 24;17:100510. doi: 10.1016/j.conctc.2019.100510. eCollection 2020 Mar.
5
Public views regarding the responsibility of patients, clinicians, and institutions to participate in research in the United States.美国公众对患者、临床医生和机构参与研究的责任的看法。
Clin Trials. 2019 Dec;16(6):574-579. doi: 10.1177/1740774519858917. Epub 2019 Jul 1.
6
Research participation preferences as expressed through a patient portal: implications of demographic characteristics.通过患者门户网站表达的研究参与偏好:人口统计学特征的影响
JAMIA Open. 2018 Oct;1(2):202-209. doi: 10.1093/jamiaopen/ooy034. Epub 2018 Aug 16.
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A population-based approach for implementing change from opt-out to opt-in research permissions.一种基于人群的方法,用于实现从退出式到加入式研究许可的转变。
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Managing clinical research permissions electronically: A novel approach to enhancing recruitment and managing consents.电子管理临床研究许可:一种增强招募和管理同意书的新方法。
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Measuring how people view biomedical research: Reliability and validity analysis of the Research Attitudes Questionnaire.衡量人们对生物医学研究的看法:《研究态度问卷》的信效度分析
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More than the money: a review of the literature examining healthy volunteer motivations.不仅仅是为了钱:一项关于健康志愿者动机的文献综述。
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公众对临床研究联络计划授权的态度。

Public attitudes toward an authorization for contact program for clinical research.

机构信息

Georgia Clinical and Translational Science Alliance, Emory University School of Medicine, Atlanta, Georgia, USA.

Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

J Am Med Inform Assoc. 2021 Feb 15;28(2):354-359. doi: 10.1093/jamia/ocaa214.

DOI:10.1093/jamia/ocaa214
PMID:33150424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7883977/
Abstract

We conducted an online experimental survey to evaluate attitudes toward an authorization for contact (AFC) program allowing researchers to contact patients about studies based on electronic record review. A total of 1070 participants were randomly assigned to 1 of 3 flyers varying in design and framing. Participants were asked to select concerns about and reasons for signing up for AFC. Logistic regression and latent class analysis were conducted. The most commonly selected concerns included needing more information (43%), privacy (40%), and needing more time to think (28%). A minority were not interested in participating in research (16%) and did not want to be bothered (15%). Latent class analysis identified clusters with specific concerns about privacy, lack of interest in research, and not wanting to be bothered. A novel flyer with simple and positive framing was associated with lower odds of both not wanting to be bothered (P = .01) and not being interested in research (P = .01). Many concerns about AFC programs appear nonspecific. Addressing privacy, lack of interest in research, and not wanting to be bothered warrant further study as ways to enhance recruitment.

摘要

我们进行了一项在线实验调查,以评估人们对授权联系(AFC)计划的态度,该计划允许研究人员基于电子病历审查联系患者进行研究。共有 1070 名参与者被随机分配到 3 种传单中的 1 种,传单在设计和框架上有所不同。参与者被要求选择签署 AFC 的关注问题和原因。我们进行了逻辑回归和潜在类别分析。最常被选中的关注问题包括需要更多信息(43%)、隐私(40%)和需要更多时间考虑(28%)。少数人对参与研究不感兴趣(16%),也不想被打扰(15%)。潜在类别分析确定了对隐私、对研究缺乏兴趣以及不想被打扰有特定关注问题的群体。具有简单积极框架的新型传单与不想被打扰(P = .01)和对研究不感兴趣(P = .01)的几率较低相关。AFC 计划的许多关注问题似乎并不具体。解决隐私、对研究缺乏兴趣和不想被打扰的问题值得进一步研究,以作为提高招募效果的方法。