Guidelines for conducting research studies with the autism community.

Autism policy & practice Pub Date : 2019-09-09
Emma Gowen, Rachel Taylor, Thomas Bleazard, Anat Greenstein, Peter Baimbridge, Daniel Poole
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Abstract

There has been growing awareness of the concern expressed by autism communities that the majority of research conducted does not reflect the priorities or needs of autistic people and their families. Further, many autistic people report that they feel unable to influence research and desire greater involvement in the research process. Our research generated practical guidelines for researchers to consider when conducting autism research, in order to increase involvement, collaboration and trust between researchers and the autism community. These guidelines are based on the output of focus groups and interview discussions with twenty-two autistic adults and eight parents of autistic children, conducted during a series of workshops carried out as a collaboration between the research network Autism@Manchester and Salfordautism, an autism support group led and run by autistic professionals. The guidelines are organised into four sections: (1) pre-study considerations, (2) recruitment of participants, (3) study visit considerations and (4) post-study considerations. These sections are structured to reflect the research pathway, to allow researchers to understand more easily how to incorporate the recommendations into their research. The recommendations promote effective communication and equal partnerships between the autism and research communities, so that the needs of participants pre-research, during and post- research are taken into account, and so that participants are supported to become involved in research at the level they choose. It is hoped that by implementing transparent and participatory approaches to their work, researchers might be able to reduce some of the dissatisfaction that members of the autism community feel towards research, leading to higher standards in autism research.

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对自闭症群体进行研究的指导方针。
越来越多的人意识到自闭症群体所表达的担忧,即大多数研究没有反映出自闭症患者及其家庭的优先事项或需求。此外,许多自闭症患者报告说,他们感到无法影响研究,并希望更多地参与研究过程。我们的研究为研究人员在进行自闭症研究时提供了实用的指导方针,以增加研究人员和自闭症社区之间的参与、合作和信任。这些指导方针是基于焦点小组的成果,以及对22名自闭症成年人和8名自闭症儿童父母的访谈讨论,这些讨论是在研究网络Autism@Manchester和索尔福德自闭症(一个由自闭症专业人士领导和运营的自闭症支持小组)合作开展的一系列研讨会期间进行的。指南分为四个部分:(1)研究前的考虑,(2)参与者的招募,(3)研究访问的考虑和(4)研究后的考虑。这些章节的结构反映了研究途径,使研究人员更容易理解如何将这些建议纳入他们的研究。这些建议促进自闭症和研究界之间的有效沟通和平等伙伴关系,以便考虑到参与者在研究前、研究中和研究后的需求,并支持参与者以他们选择的水平参与研究。希望通过在工作中实施透明和参与性的方法,研究人员能够减少自闭症社区成员对研究的一些不满,从而提高自闭症研究的标准。
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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Guidelines for conducting research studies with the autism community.
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