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寻觅却无果(目前):在临床试验注册库中查找以患者为导向设计的试验——行动呼吁

Seek and Ye Shall Not Find (Yet): Searching Clinical Trial Registries for Trials Designed With Patients-A Call to Action.

作者信息

Woolley Karen Louise, Woolley J D, Woolley Mark James

机构信息

Faculty of Health, Medicine and Behavioural Sciences, University of Queensland, St Lucia, Brisbane, 4067, Australia, 61 7 3365 7489.

Clinical Trials Centre, University of the Sunshine Coast, Sippy Downs, Australia.

出版信息

J Particip Med. 2025 May 30;17:e72015. doi: 10.2196/72015.

Abstract

Clinical trial registries were designed to help patients search for potentially suitable clinical trials. When our family faced another serious cancer diagnosis, we searched multiple international clinical trial registries. Despite increasing evidence that trials designed with patients can be better for trial participants (eg, they can have more relevant outcome measures and fewer burdens), it is currently impossible to search registries for these specific types of trials. In this Patient Perspective article, we make the first "call to action" for clinical trial registries to include (1) a filter that allows for efficient searching for clinical trials designed with patients and (2) structured information, in plain language, on how patients were involved. We propose how these two innovations could help reduce barriers to clinical trial participation. We also highlight how new regulatory and ethical guidelines are encouraging patient involvement in trial design, and we identify the benefits to many of doing so. Given the pressing need to improve clinical trial participation, we respectfully call on the clinical trial community to respond to our call to action and consider our proposed action plan. Ideally, when patients want to search for clinical trials designed with patients for patients, we should be able to find them. A plain language summary for this publication is available in the supplementary material for this paper.

摘要

临床试验注册库旨在帮助患者寻找可能合适的临床试验。当我们家面临另一个严重的癌症诊断时,我们搜索了多个国际临床试验注册库。尽管越来越多的证据表明,为患者设计的试验对试验参与者可能更好(例如,它们可以有更相关的结果指标且负担更小),但目前无法在注册库中搜索这些特定类型的试验。在这篇患者视角文章中,我们首次向临床试验注册库发出“行动呼吁”,要求其纳入:(1)一个过滤器,以便能够高效搜索为患者设计的临床试验;(2)以通俗易懂的语言提供关于患者如何参与的结构化信息。我们提出这两项创新如何有助于减少临床试验参与的障碍。我们还强调新的监管和伦理指南如何鼓励患者参与试验设计,并指出这样做对许多人带来的好处。鉴于改善临床试验参与的迫切需求,我们郑重呼吁临床试验界响应我们的行动呼吁,并考虑我们提出的行动计划。理想情况下,当患者想要搜索为患者设计的、供患者参与的临床试验时,我们应该能够找到它们。本文的补充材料中有该出版物的通俗易懂的摘要。

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