Stakeholder perspectives on data sharing from pragmatic clinical trials: Unanticipated challenges for meeting emerging requirements

IF 2.6 Q2 HEALTH POLICY & SERVICES
Stephanie R. Morain, Juli Bollinger, Kevin Weinfurt, Jeremy Sugarman
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引用次数: 0

Abstract

Introduction

Numerous arguments have been advanced for broadly sharing de-identified, participant-level clinical trial data. However, data sharing in pragmatic clinical trials (PCTs) presents ethical challenges. While prior scholarship has described aspects of PCTs that raise distinct considerations for data sharing, there have been no reports of the experiences of those at the leading edge of data-sharing efforts for PCTs, including how these particular challenges have been navigated. To address this gap, we conducted interviews with key stakeholders, with a focus on the ethical issues presented by sharing data from PCTs.

Methods

We recruited respondents using purposive sampling to reflect the range of stakeholder groups affected by efforts to expand PCT data sharing. Through semi-structured interviews, we explored respondents' experiences and perceptions about sharing de-identified, individual-level data from PCTs. An integrated approach was used to identify and describe key themes.

Results

We conducted 40 interviews between April and September 2022. Five overarching themes emerged through analysis: (1) challenges in sharing data collected under a waiver or alteration of consent; (2) conflicting views regarding PCT patient-subject preferences for data sharing; (3) identification of respect-promoting practices beyond consent; (4) concerns about elevated risks or burdens from sharing PCT data; and (5) diverse views about the likely benefits resulting from sharing PCT data.

Conclusion

Our data indicate unresolved tensions in how to fulfill the expectation to broadly share de-identified, individual-level data from PCTs, and suggest that those promulgating and implementing data-sharing policies must be sensitive to PCT-specific considerations. Future work could inform efforts to tailor data-sharing policy and practice to reflect the challenges presented by PCTs, including sharing experiences from trials that have successfully navigated these tensions.

利益相关者对务实临床试验数据共享的看法:满足新需求的意外挑战
导言:对于广泛共享去标识化、参与者水平的临床试验数据,人们提出了许多论据。然而,实用临床试验(PCT)中的数据共享面临着伦理挑战。虽然之前的学术研究已经描述了 PCT 在数据共享方面需要特别考虑的方面,但还没有关于处于 PCT 数据共享工作前沿的人员的经验,包括如何应对这些特殊挑战的报告。为了填补这一空白,我们对主要利益相关者进行了访谈,重点关注 PCT 数据共享带来的伦理问题。 方法 我们采用目的性抽样的方式招募受访者,以反映受扩大 PCT 数据共享工作影响的利益相关者群体的范围。通过半结构式访谈,我们探究了受访者对于共享来自 PCT 的去标识化个人层面数据的经验和看法。我们采用了一种综合方法来识别和描述关键主题。 结果 我们在 2022 年 4 月至 9 月期间进行了 40 次访谈。通过分析,我们发现了五大主题:(1) 分享在放弃或更改同意书的情况下收集的数据所面临的挑战;(2) 关于 PCT 患者-受试者数据共享偏好的意见冲突;(3) 识别同意书之外的促进尊重的做法;(4) 担心分享 PCT 数据会增加风险或负担;(5) 对分享 PCT 数据可能带来的益处有不同看法。 结论 我们的数据表明,在如何实现广泛共享来自 PCT 的去标识化个人层面数据的期望方面,存在着尚未解决的矛盾,并表明颁布和实施数据共享政策者必须对 PCT 的具体考虑因素保持敏感。未来的工作可以为调整数据共享政策和实践提供信息,以反映PCT带来的挑战,包括分享成功应对这些矛盾的试验经验。
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来源期刊
Learning Health Systems
Learning Health Systems HEALTH POLICY & SERVICES-
CiteScore
5.60
自引率
22.60%
发文量
55
审稿时长
20 weeks
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