Suppr超能文献

将残疾人排除在临床研究之外:资格标准缺乏清晰度和正当性。

Excluding People With Disabilities From Clinical Research: Eligibility Criteria Lack Clarity And Justification.

机构信息

Willyanne DeCormier Plosky, Brigham and Women's Hospital, Boston, Massachusetts.

Ari Ne'eman, Harvard University, Cambridge, Massachusetts.

出版信息

Health Aff (Millwood). 2022 Oct;41(10):1423-1432. doi: 10.1377/hlthaff.2022.00520.

Abstract

The exclusion of people with disabilities from clinical research without appropriate justification is discriminatory, is counter to federal regulations and research guidelines, and limits study generalizability. This matter is understudied, and data on the disability status of trial participants are rarely collected or reported. We analyzed ninety-seven recent interventional protocols in four therapeutic areas registered on ClinicalTrials.gov. Eighty-five percent of protocols allowed broad investigator discretion to determine eligibility, whereas only 18 percent explicitly permitted people with disabilities to use forms of support (such as supported decision making or assistive devices) to facilitate study participation. Eligibility criteria affecting people with disabilities included exclusions for psychiatric (68 percent), substance use (62 percent), HIV or hepatitis (53 percent), cognitive or intellectual (42 percent), visual (34 percent), hearing (10 percent), mobility (9 percent), long-term care (6 percent), and speech and communication (3 percent) disability-related domains. Documented justification was provided for only 24 percent of these exclusions. We recommend greater scrutiny of study eligibility criteria, scientific or ethical justification of exclusions, and accessible study design.

摘要

将残疾人排除在临床研究之外而没有适当的理由是歧视性的,违反了联邦法规和研究指南,并限制了研究的普遍性。这个问题研究得还不够充分,很少有研究收集或报告试验参与者的残疾状况数据。我们分析了 ClinicalTrials.gov 上登记的四个治疗领域的 97 项最近的干预性方案。85%的方案允许研究人员广泛决定资格,而只有 18%明确允许残疾人使用支持(如支持性决策或辅助设备)来促进研究参与。影响残疾人的资格标准包括对精神疾病(68%)、药物滥用(62%)、艾滋病毒或肝炎(53%)、认知或智力(42%)、视力(34%)、听力(10%)、行动能力(9%)、长期护理(6%)以及言语和沟通(3%)等残疾相关领域的排除。对于这些排除,只有 24%提供了有记录的正当理由。我们建议更仔细地审查研究资格标准、排除的科学或伦理依据,以及可访问的研究设计。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验