Parents’ Perspectives on Participating in Genetic Research in Autism

被引:0
|
作者
Magan Trottier
Wendy Roberts
Irene Drmic
Stephen W. Scherer
Rosanna Weksberg
Cheryl Cytrynbaum
David Chitayat
Cheryl Shuman
Fiona A. Miller
机构
[1] The Hospital for Sick Children,Division of Clinical and Metabolic Genetics
[2] University of Toronto,Department of Molecular Genetics
[3] The Hospital for Sick Children,Autism Research Unit
[4] Holland Bloorview Kids Rehabilitation Hospital,Department of Pediatrics
[5] University of Toronto,Program in Genetics and Genome Biology
[6] The Centre for Applied Genomics,Department of Obstetrics and Gynecology
[7] The Hospital for Sick Children,Institute of Health Policy, Management and Evaluationred
[8] The Hospital for Sick Children,undefined
[9] The Prenatal Diagnosis and Medical Genetics Program,undefined
[10] Mount Sinai Hospital,undefined
[11] University of Toronto,undefined
来源
Journal of Autism and Developmental Disorders | 2013年 / 43卷
关键词
Autism; Parent experiences; Genetic research; Motivations; Expectations; Genetic result;
D O I
暂无
中图分类号
学科分类号
摘要
Genetic research in autism depends on the willingness of individuals with autism to participate; thus, there is a duty to assess participants’ needs in the research process. We report on families’ motives and expectations related to their participation in autism genetic research. Respondents valued having a genetic result, as it alleviates guilt, promotes awareness, and may be used to tailor interventions and for family planning. The act of participating was distinctly significant, as it provided personal control, a connection to autism experts, networking with families, and hope for the future. The results of this study highlight complex factors involved in families’ decisions to participate in autism genetic research and provide points to consider for this population of research participants.
引用
收藏
页码:556 / 568
页数:12
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