共同设计一种新的服务提供途径,以增加在一个非营利性社区组织中获得自闭症识别和护理的机会,该组织为文化和语言不同的家庭服务。

IF 5.6 2区 心理学 Q1 PSYCHOLOGY, DEVELOPMENTAL
Autism Pub Date : 2025-08-01 Epub Date: 2025-05-09 DOI:10.1177/13623613251335702
Shana M Attar, Hannah Benavidez, Carol Gicheru, Colleen Alabi, Risho Sapano, Wendy L Stone
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引用次数: 0

摘要

与非文化和语言不同的家庭相比,文化和语言不同的家庭在获得及时的自闭症专业护理方面面临更大的挑战,最终的健康结果也不太理想。需要为文化和语言多样化的家庭提供自闭症护理的其他途径;然而,一种新途径的特征尚不清楚。一个共同设计的过程是与一个文化嵌入式非营利社区组织开发一个新的服务提供途径,以增加美国文化和语言不同的家庭获得自闭症服务的机会。23个人参加了8个2小时的共同设计会议。参与者包括一线工作人员(7名非专业提供者)、管理领导(2名项目主管和2名组织主管)、来自7个未被充分研究的文化和语言群体(即索马里麦麦语、斯瓦希里语、阿拉伯语、达里语/普什图语、法语、阿姆哈拉语和提格里亚语)的8名最终用户(护理人员)和4名自闭症专家。共同设计确定了五个关键的设计特征:尊重多样性、优先照顾者代理、增加可及性、最小化污名和最大化可行性。这些特点促使我们共同开发了一种新的途径,为文化和语言不同的家庭提供自闭症识别和护理,将导航服务与传播简短、文化敏感、循证的育儿和应对策略相结合。这种权力分享、社区-学术伙伴关系可以作为改善自闭症护理公平性的一种模式。早期,专门的支持对于帮助自闭症儿童学习和发展是非常重要的。然而,来自不同文化背景的家庭往往发现很难获得这种早期帮助。一个大学实验室和一个社区组织合作,为这些家庭创造了一种获得自闭症服务的新途径。我们采用了共同设计的方法,包括从参与自闭症护理的各种人那里收集反馈,包括服务提供者、社区领袖、护理人员和自闭症专家。23个人参加了8次共同设计会议,每次会议2小时。参与者来自不同的语言群体,包括索马里麦麦语、斯瓦希里语、阿拉伯语、达里语/普什图语、法语、阿姆哈拉语和提格里亚语。这些会议帮助我们确定了改善获得所需服务的五个重要因素:注意群体之间的文化差异,赋予护理人员权力,为获得服务提供信息和支持,减少对自闭症的污名化,并确保服务可实际使用。基于这些因素,我们开发了一种新的途径,让家庭获得自闭症护理。这种新方法包括在医疗和教育系统中提供帮助,并为育儿和应对提供简短、文化上适当的建议。这个项目展示了如何与社区合作可以创造更公平和有效的方式来提供自闭症支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-designing a novel service delivery pathway to increase access to autism identification and care within a non-profit community organization serving culturally and linguistically diverse families.

Culturally and linguistically diverse families experience greater challenges accessing timely, autism-specialized care relative to non-culturally and linguistically diverse families, and ultimately experience less optimal health outcomes. Alternative pathways to access autism care for culturally and linguistically diverse families are needed; however, the features of a novel pathway remain unclear. A co-design process was used with a culturally embedded non-profit community organization to develop a novel service delivery pathway for increasing access to autism services for culturally and linguistically diverse families in the United States. Twenty-three individuals participated in eight, 2-hour co-design sessions. Participants included front-line staff (seven non-specialist providers), management leaders (two program supervisors and two organization directors), and eight end-users (caregivers) from seven understudied cultural and linguistic groups (i.e. Somali Mai Mai, Swahili, Arabic, Dari/Pashto, French, Amharic, and Tigrinya) and four autism specialists. The co-design identified five key design features: respecting diversity, prioritizing caregiver agency, increasing accessibility, minimizing stigma, and maximizing feasibility. These features informed the co-development of a novel pathway to access autism identification and care for culturally and linguistically diverse families that pairs navigation services with the dissemination of brief, culturally sensitive, and evidence-based parenting and coping strategies. This power-sharing, community-academic partnership may serve as a model for improving equity in autism care.Lay AbstractEarly, specialized support is important for helping young autistic children learn and develop. However, families from different cultural backgrounds often find it challenging to access this early help. A university lab and a community organization worked together to create a new way for these families to access autism services. We used a co-design approach, which involves gathering feedback from a variety of people involved in autism care, including service providers, community leaders, caregivers, and autism experts. Twenty-three individuals participated in eight co-design sessions that were two hours each. Participants were from different language groups, including Somali Mai Mai, Swahili, Arabic, Dari/Pashto, French, Amharic, and Tigrinya. These sessions helped us identify five important factors important for improving access to needed services: being mindful about cultural differences between groups, empowering caregivers, providing information and support for accessing services, reducing stigma around autism, and ensuring the service is practical to use. Based on these factors, we developed a new pathway for families to access autism care. This new approach includes providing help in navigating the medical and educational systems and provides short, culturally appropriate advice for parenting and coping. This project shows how working together with communities can create more fair and effective ways to provide autism support.

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来源期刊
Autism
Autism PSYCHOLOGY, DEVELOPMENTAL-
CiteScore
9.80
自引率
11.50%
发文量
160
期刊介绍: Autism is a major, peer-reviewed, international journal, published 8 times a year, publishing research of direct and practical relevance to help improve the quality of life for individuals with autism or autism-related disorders. It is interdisciplinary in nature, focusing on research in many areas, including: intervention; diagnosis; training; education; translational issues related to neuroscience, medical and genetic issues of practical import; psychological processes; evaluation of particular therapies; quality of life; family needs; and epidemiological research. Autism provides a major international forum for peer-reviewed research of direct and practical relevance to improving the quality of life for individuals with autism or autism-related disorders. The journal''s success and popularity reflect the recent worldwide growth in the research and understanding of autistic spectrum disorders, and the consequent impact on the provision of treatment and care. Autism is interdisciplinary in nature, focusing on evaluative research in all areas, including: intervention, diagnosis, training, education, neuroscience, psychological processes, evaluation of particular therapies, quality of life issues, family issues and family services, medical and genetic issues, epidemiological research.
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