Consensus recommendations for usability and acceptability of mobile health autism screening tools.

IF 5.6 2区 心理学 Q1 PSYCHOLOGY, DEVELOPMENTAL
Autism Pub Date : 2025-08-12 DOI:10.1177/13623613251360276
Gabriella Tangkilisan, Luis Rivas Vazquez, Plyce Fuchu, Benjamin Sanders, Jill K Dolata, Steven Bedrick, Eric Fombonne, Sarabeth Broder-Fingert, Katharine E Zuckerman
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引用次数: 0

Abstract

Mobile health (mHealth; online phone or tablet-based) screening tools for autism are being increasingly used by parents, health care, and educational providers. However, it is unclear whether mHealth autism screening will improve the inequalities in autism or further help individuals already advantaged in autism care. To try to improve equity in mHealth autism screening, we conducted a modified Delphi consensus panel process with 14 panelists who were medical providers, parents, tool developers, and educational providers. Panelists participated in three asynchronous online voting rounds followed by online discussions. Panelists were provided a preliminary list of 28 recommendations for autism-screening tools that were compiled from previous qualitative interviews in the larger project. In each round, panelists were asked to vote for up to 10 recommendations from the preliminary list and discuss the voting results. After the third round of asynchronous voting, a final round of discussion with all the panelists was held live through Zoom to discuss the final asynchronous voting results. All voting and discussion took place on an online app called Slack. Voting and discussion yielded 19 recommendations in five conceptual categories: transparency, equity, access, product design and user experience, and development process. Tools adhering to these recommendations may increase equitable service use after screening.Lay abstractFamilies may use information online to learn more about autism. Families, health care, and educational providers may use online tools like checklists or web apps to screen for autism (measure whether a young child has autism symptoms or behaviors). However, we do not know whether the online autism-screening tools can be easily used by families and providers. It is possible that families who are culturally diverse, have lower education, or have lower income have trouble using online autism-screening tools. We conducted an online consensus panel with medical/educational providers, parents, and tool developers, asking them to vote and have discussions on suggestions for online screening tools for autism. The voting and discussions resulted in 19 suggestions for changes to make the tools easier to use. The top recommendations included directly linking to sources of information about autism, reading level that is less than or equal to fifth grade, and focusing on the diverse behavior/needs/strengths associated with autism.

关于移动健康自闭症筛查工具的可用性和可接受性的共识建议。
移动医疗(mHealth;父母、医疗保健和教育提供者越来越多地使用在线(手机或平板电脑)自闭症筛查工具。然而,目前尚不清楚移动健康自闭症筛查是否会改善自闭症中的不平等现象,或进一步帮助已经在自闭症护理中处于优势的个体。为了提高移动健康自闭症筛查的公平性,我们进行了一个改进的德尔菲共识小组程序,由14名小组成员组成,他们是医疗服务提供者、家长、工具开发人员和教育提供者。小组成员参加了三轮异步在线投票,随后进行了在线讨论。小组成员被提供了一份初步清单,其中包括28项自闭症筛查工具的建议,这些建议是根据之前在更大项目中的定性访谈编制的。在每一轮中,小组成员被要求从初步名单中投票选出最多10项建议,并讨论投票结果。在第三轮异步投票后,通过Zoom与所有小组成员进行最后一轮讨论,讨论最终的异步投票结果。所有的投票和讨论都是在一个名为Slack的在线应用程序上进行的。投票和讨论产生了5个概念类别的19条建议:透明度、公平、访问、产品设计和用户体验以及开发过程。遵循这些建议的工具可能会增加筛查后服务的公平使用。家庭可以利用网上的信息来了解更多关于自闭症的信息。家庭、医疗保健和教育提供者可能会使用在线工具,如检查表或网络应用程序来筛查自闭症(测量幼儿是否有自闭症症状或行为)。然而,我们不知道在线自闭症筛查工具是否可以被家庭和提供者轻松使用。有可能是文化多样化、受教育程度较低或收入较低的家庭在使用在线自闭症筛查工具方面存在困难。我们与医疗/教育提供者、家长和工具开发者进行了一个在线共识小组,请他们投票并讨论关于自闭症在线筛查工具的建议。投票和讨论产生了19条修改建议,以使工具更易于使用。最重要的建议包括直接链接到有关自闭症的信息来源,阅读水平低于或等于五年级,以及关注与自闭症相关的各种行为/需求/优势。
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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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