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解决数字临床试验中的健康不平等问题:从 HIV 研究领域看挑战与解决方案。

Addressing Health Inequities in Digital Clinical Trials: A Review of Challenges and Solutions From the Field of HIV Research.

出版信息

Epidemiol Rev. 2022 Dec 21;44(1):87-109. doi: 10.1093/epirev/mxac008.

Abstract

Clinical trials are considered the gold standard for establishing efficacy of health interventions, thus determining which interventions are brought to scale in health care and public health programs. Digital clinical trials, broadly defined as trials that have partial to full integration of technology across implementation, interventions, and/or data collection, are valued for increased efficiencies as well as testing of digitally delivered interventions. Although recent reviews have described the advantages and disadvantages of and provided recommendations for improving scientific rigor in the conduct of digital clinical trials, few to none have investigated how digital clinical trials address the digital divide, whether they are equitably accessible, and if trial outcomes are potentially beneficial only to those with optimal and consistent access to technology. Human immunodeficiency virus (HIV), among other health conditions, disproportionately affects socially and economically marginalized populations, raising questions of whether interventions found to be efficacious in digital clinical trials and subsequently brought to scale will sufficiently and consistently reach and provide benefit to these populations. We reviewed examples from HIV research from across geographic settings to describe how digital clinical trials can either reproduce or mitigate health inequities via the design and implementation of the digital clinical trials and, ultimately, the programs that result. We discuss how digital clinical trials can be intentionally designed to prevent inequities, monitor ongoing access and utilization, and assess for differential impacts among subgroups with diverse technology access and use. These findings can be generalized to many other health fields and are practical considerations for donors, investigators, reviewers, and ethics committees engaged in digital clinical trials.

摘要

临床试验被认为是确定卫生干预措施疗效的金标准,从而决定将哪些干预措施纳入医疗保健和公共卫生计划中推广。广义上的数字临床试验是指在实施、干预措施和/或数据收集过程中部分或完全整合技术的试验,其价值在于提高效率以及测试数字交付的干预措施。尽管最近的综述描述了数字临床试验的优缺点,并为提高数字临床试验的科学严谨性提供了建议,但很少有研究调查数字临床试验如何解决数字鸿沟问题,它们是否公平可及,以及试验结果是否仅对那些具有最佳和一致技术获取能力的人有利。人类免疫缺陷病毒(HIV)和其他健康状况一样,不成比例地影响到社会和经济边缘化人群,这引发了一个问题,即在数字临床试验中发现有效的干预措施并随后推广到这些人群时,是否能够充分和持续地惠及这些人群。我们从不同地理环境的 HIV 研究中选取了一些例子,描述了数字临床试验可以通过数字临床试验的设计和实施,以及最终产生的项目,来重现或减轻健康不平等现象。我们讨论了数字临床试验如何能够被有意设计用于预防不平等现象,监测持续的获取和利用情况,并评估不同技术获取和使用群体之间的差异影响。这些发现可以推广到许多其他健康领域,对于参与数字临床试验的捐赠者、研究人员、评审人员和伦理委员会来说,都是实际需要考虑的问题。

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