"It Is Easy Using My Apps:" Understanding Technology Use and Needs of Adults with Down Syndrome
Hailey L. Johnson, Audra Sterling, Bilge Mutlu
TL;DR
This paper addresses the gap in understanding how adults with Down syndrome use technology and what they need from assistive tech. Using semi-structured, dyadic interviews with six adults with DS, seven parents, and three experts, the study employs Reflexive Thematic Analysis to derive four DS-centered design themes: community versus home social involvement, misalignment of skill expectations, family limitations in technology support, and considerations for technology development. The findings reveal nuanced preferences for privacy, variable views on speech and literacy supports, and the central role of families in early adoption, followed by independent use, informing four concrete design implications: positive reinforcement, multimodal interactions, clear instructional visuals, and adaptable privacy features. These insights advance DS-specific adult-oriented assistive technology design, offering actionable guidance for developers and policymakers to enhance independence, safety, and social inclusion for adults with DS.
Abstract
Assistive technologies for adults with Down syndrome (DS) need designs tailored to their specific technology requirements. While prior research has explored technology design for individuals with intellectual disabilities, little is understood about the needs and expectations of adults with DS. Assistive technologies should leverage the abilities and interests of the population, while incorporating age- and context-considerate content. In this work, we interviewed six adults with DS, seven parents of adults with DS, and three experts in speech-language pathology, special education, and occupational therapy to determine how technology could support adults with DS. In our thematic analysis, four main themes emerged, including (1) community vs. home social involvement; (2) misalignment of skill expectations between adults with DS and parents; (3) family limitations in technology support; and (4) considerations for technology development. Our findings extend prior literature by including the voices of adults with DS in how and when they use technology.
