A Passing Problem: Evaluating Harm and Benefit in Autism Research

Q2 Social Sciences
Ari Ne'eman, Kenneth A. Richman, Allison M. McCarthy, Daniel Wilkenfeld
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引用次数: 0

Abstract

Autism research frequently seeks to evaluate interventions or inform their development. Unfortunately, researchers often assume that autism intervention should reduce autistic traits, effectively setting as a goal of treatment that autistic people attempt to “pass” as nonautistic. A growing body of evidence highlights serious potential harms from passing demands. We discuss why it is important for institutional review boards (IRBs) to scrutinize autism research for clinical passing demands, and we document the existence of such demands in outcome measures commonly employed in autism research. We propose an ethical framework for IRBs and others to make use of in evaluating the ethical appropriateness of particular treatment goals in autism intervention or intervention-adjacent research, emphasizing that treatment goals should be in pursuit of a beneficial nonpassing purpose and be the least burdensome means of accomplishing such a purpose. We also highlight potential promising practices for IRBs, investigators, and other stakeholders seeking to address these issues in autism research.

一个过时的问题:评估自闭症研究中的危害和益处。
自闭症研究经常寻求评估干预措施或为其发展提供信息。不幸的是,研究人员经常假设自闭症干预应该减少自闭症的特征,有效地设定了一个治疗目标,自闭症患者试图“通过”非自闭症。越来越多的证据表明,不通过的要求可能带来严重的潜在危害。我们讨论了为什么机构审查委员会(irb)审查自闭症研究的临床通过需求是重要的,我们在自闭症研究中常用的结果测量中记录了这些需求的存在。我们提出了一个伦理框架,用于评估自闭症干预或干预相关研究中特定治疗目标的伦理适宜性,强调治疗目标应该追求有益的非通过目的,并且是实现这一目的的负担最小的手段。我们还强调了irb、研究者和其他利益相关者在自闭症研究中寻求解决这些问题的潜在有前途的实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ethics & human research
Ethics & human research Social Sciences-Health (social science)
CiteScore
2.90
自引率
0.00%
发文量
35
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