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User Requirements for Comanaged Digital Health and Care: Review
Chaloner Chute1, Tara French2, Sneha Raman2
1The Digital Health & Care Innovation Centre, University of Strathclyde, Glasgow, United Kingdom.
Digital tools can support sustainable health and social care by shifting focus to community-based, person-centered models. Key user requirements emphasize data co-management for improved care and citizen control over personal health information.
Area of Science:
- Digital Health and Care
- Human-Computer Interaction
- Participatory Design
Background:
- The sustainability of health and social care necessitates a shift towards community-based, person-centered, integrated, and preventive models.
- Digital tools are crucial for this transition but must encompass broader personal, social, and environmental needs beyond a purely clinical focus.
- Existing literature often lacks a whole-system or whole-of-life perspective in digital health and care design.
Purpose of the Study:
- To identify recurring user requirements and themes for co-managed digital health and care services.
- To facilitate a shift from system-led, condition-specific approaches to person-centric, whole-of-life health and care models.
- To inform the design and delivery of digital health and care services.
Main Methods:
- Employed participatory design as the core methodological approach.
- Conducted a structured review of co-design projects within a digital health and care program.
- Utilized a selection framework to identify eligible projects for user requirement derivation.
Main Results:
- Identified 14 common user requirements from a review of co-design projects.
- Found overlapping needs between citizens and care professionals regarding data co-management for improved outcomes.
- Highlighted consensus on personal health storytelling, sharing care experiences, personalized guidance, and improved dialogue, while noting gaps in group engagement and siloed organizational structures.
Conclusions:
- Recommends privacy-preserving digital infrastructure empowering citizens as active partners in managing their health data and care.
- Advocates for incorporating broader user requirement contexts into the development of new digital services.
- Stresses the need for further research into trust frameworks for citizen data co-management across diverse formal and informal actors.
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