Partnering With a Purpose: Promoting Equity and Justice for Black Children With Autism Spectrum Disorder.

IF 1.8 3区 医学 Q3 BEHAVIORAL SCIENCES
Stephanie Castelin, Josselyn Okorodudu, Teresa Smith
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引用次数: 0

Abstract

Objective: Black children with autism and their families face disparities within clinical care and services, leading to inequitable health outcomes. However, there is limited research centering the voices of the Black autism community in understanding how to address these inequities. In this study, researchers explored the perspectives of caregivers of Black children with autism regarding barriers to equitable care and recommendations for improved services.

Methods: Community leaders from an autism advocacy group and researchers from a large academic medical center partnered to conduct a Group Level Assessment with 31 Black families of children with autism. During a three-hour research event, participants discussed their experiences within community, school, and clinical services, collectively coded and interpreted the data, and generated action steps to improve services.

Results: The findings revealed 6 areas of need regarding the services Black children with autism and their caregivers receive. Black caregivers recommended that systems of care improve access to culturally responsive care, integrate caregiver priorities within their care, and engage in collaborative decision-making with caregivers. Providers should also equip caregivers with an accessible roadmap for navigating their child's services and connect them to care management professionals and resources for mental health support.

Conclusion: The findings of this study address a critical gap in the literature by partnering with the Black autism community to identify solutions to address their needs; these recommendations can be used as a foundation for service providers to reduce disparities and improve outcomes for Black children with autism and their families.

有目的的合作:促进自闭症谱系障碍黑人儿童的平等与公正。
目的:患有自闭症的黑人儿童及其家庭在临床护理和服务方面面临着差异,导致了不公平的健康结果。然而,以黑人自闭症群体的声音为中心来了解如何解决这些不平等问题的研究却很有限。在本研究中,研究人员探讨了黑人自闭症儿童照顾者对公平护理障碍的看法以及对改善服务的建议:方法:一个自闭症倡导团体的社区领袖和一个大型学术医疗中心的研究人员合作,对 31 个黑人自闭症儿童家庭进行了一次团体水平评估。在三小时的研究活动中,参与者讨论了他们在社区、学校和临床服务中的经历,对数据进行了集体编码和解释,并提出了改善服务的行动步骤:结果:研究结果显示,黑人自闭症儿童及其照护者在接受服务方面有 6 个需求领域。黑人照护者建议,照护系统应改善文化适应性照护的获取途径,将照护者的优先事项纳入其照护范围,并与照护者共同参与决策。医疗服务提供者还应为照护者提供一份便于使用的路线图,以指导他们为孩子提供服务,并将他们与护理管理专业人员和心理健康支持资源联系起来:本研究的结论通过与黑人自闭症社区合作,找出满足他们需求的解决方案,填补了文献中的一个重要空白;这些建议可作为服务提供者减少差异和改善黑人自闭症儿童及其家庭治疗效果的基础。
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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来源期刊
CiteScore
3.10
自引率
8.30%
发文量
155
审稿时长
6-12 weeks
期刊介绍: Journal of Developmental & Behavioral Pediatrics (JDBP) is a leading resource for clinicians, teachers, and researchers involved in pediatric healthcare and child development. This important journal covers some of the most challenging issues affecting child development and behavior.
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