Autistic eye contact? A hermeneutic phenomenological multicenter study of the similarities and differences in eye-contact experiences between adults with and without autism.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Jos Boer, Nynke Boonstra, Linda Kronenberg, Sonja Kuipers, Richard Vuijk, Bram Sizoo
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引用次数: 0

Abstract

Eye contact is one of the most important forms of interpersonal communication. Nonetheless, research has shown that there is no gold standard for how eye contact should occur. Atypicalities in eye contact are one of the core features of autism spectrum disorder (ASD), but there is still no consensus on what constitutes atypical eye contact in ASD. The current research explores both the breadth and depth of experiences with eye contact in adults with and without ASD. We used a hermeneutic phenomenological multicenter design in which 15 adults with ASD and 15 adults without ASD were interviewed. Analyses using Multisite Qualitative Analysis (MSQA) and the PRICE model for saturation identified four themes: opinion on eye contact, experience of eye contact, approach toward eye contact, and needs regarding eye contact. Adults with and without ASD appeared to have overlapping and distinct experiences. This study provides the first insights into similarities and differences in experiences with eye contact in adults with and without ASD. The results provide guidance for future research and for the development of interventions to reduce problems arising from eye contact in ASD.

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自闭症的眼神交流?自闭症成人与非自闭症成人眼神接触经验异同的解释学现象学多中心研究。
眼神交流是人际交往中最重要的形式之一。尽管如此,研究表明,对于眼神交流应该如何进行并没有黄金标准。目光接触的非典型性是自闭症谱系障碍(ASD)的核心特征之一,但对于ASD的非典型性目光接触的构成仍未达成共识。目前的研究探索了有和没有自闭症的成年人眼神交流的广度和深度。我们采用解释学现象学多中心设计,对15名自闭症成年人和15名非自闭症成年人进行了访谈。使用多站点定性分析(MSQA)和饱和度的PRICE模型进行分析,确定了四个主题:对眼神接触的看法、眼神接触的经验、眼神接触的方法和对眼神接触的需求。有和没有ASD的成年人似乎有重叠和不同的经历。这项研究首次揭示了自闭症患者和非自闭症患者在眼神交流方面的异同。这些结果为未来的研究和干预措施的发展提供了指导,以减少ASD患者眼神接触引起的问题。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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