"I Knew She'd Get It, and Get Me": Participants' Perspectives of a Participatory Autism Research Project.

Elizabeth Pellicano, Wenn Lawson, Gabrielle Hall, Joanne Mahony, Rozanna Lilley, Melanie Heyworth, Hayley Clapham, Michael Yudell
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Abstract

Introduction: Autistic advocates and their supporters have long argued that conventional research practices provide too few opportunities for genuine engagement with autistic people, contributing to social disenfranchisement among autistic people. We recently described one attempt to develop and implement a participatory study in which a team of autistic and nonautistic researchers worked together to gather life histories from late-diagnosed autistic people. In the current study, we sought to understand the impact of this participatory approach on the participants themselves.

Methods: We spoke to 25 Australian late-diagnosed autistic adults (aged 45-72 years), who had been interviewed by an autistic researcher using an oral history approach. We asked them about their experience of being involved in that project and the research process more broadly. We thematically analyzed participants' interviews.

Results: Participants responded overwhelmingly positively to the opportunity to tell their life history, considering it illuminating and empowering. While recounting their life history was often described as "exhausting" and "draining," participants also reported feeling "supported all the way" and agreed "it was made easier because I had an autistic researcher interviewing me." One participant went so far as to say that they "probably would have dropped out [of the project] if it was run by people who weren't autistic."

Conclusions: These findings demonstrate that the benefits of coproduction to researchers and community partners extend to study participants and to the quality of the research itself. Involving autistic partners in the research process, especially in its implementation, can play a crucial role in enhancing autism research.

Abstract Image

"我知道她会明白的,也会明白我的:参与者对自闭症参与式研究项目的看法。
导言:长期以来,自闭症倡导者及其支持者一直认为,传统的研究方法为自闭症患者提供的真正参与机会太少,导致自闭症患者的社会权利被剥夺。最近,我们描述了一次开发和实施参与式研究的尝试,在这项研究中,一个由自闭症和非自闭症研究人员组成的团队共同合作,从晚期确诊的自闭症患者那里收集生活史。在本研究中,我们试图了解这种参与式研究方法对参与者本身的影响:我们与 25 名澳大利亚晚期确诊自闭症成年人(45-72 岁)进行了交谈,自闭症研究人员采用口述历史的方法对他们进行了采访。我们询问了他们参与该项目的经历以及更广泛的研究过程。我们对参与者的访谈进行了主题分析:结果:参与者对有机会讲述自己的生活史反应非常积极,认为这很有启发性,也很有力量。虽然讲述自己的人生经历常常被描述为 "令人筋疲力尽 "和 "耗尽精力",但参与者也表示感觉 "一直得到支持",并同意 "因为有一位自闭症研究人员对我进行访谈,这一切都变得容易多了"。一位参与者甚至说,"如果项目是由非自闭症患者主持的,他们可能就会退出(项目)":这些研究结果表明,合作研究对研究人员和社区合作伙伴的益处不仅体现在研究参与者身上,还体现在研究本身的质量上。让自闭症合作伙伴参与研究过程,尤其是研究的实施过程,可以在加强自闭症研究方面发挥至关重要的作用。
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