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Updated: Jan 8, 2026

Exergaming in Older People Living with HIV Improves Balance, Mobility and Ameliorates Some Aspects of Frailty
Published on: October 6, 2016
What do I want my providers to know? Co-designing education with older adults living with HIV
Kristina M Kokorelias1, Christine Sheppard2, Dean Valentine3
1Section of Geriatric Medicine, Department of Medicine, Sinai Health System and University Health Network, Toronto, Ontario, Canada; Department of Occupational Science & Occupational Therapy, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada; National Institute on Ageing, Toronto Metropolitan University, Toronto, Ontario, Canada; Rehabilitation Sciences Institute, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Objectives:
To co-design an educational resource for primary healthcare providers in partnership with older adults living with HIV, with the aim of addressing key gaps in provider knowledge and enhancing the delivery of holistic, person-centered care.
Methods:
A qualitative descriptive study using a co-design methodology was conducted with 12 older adults (aged ≥50) living with HIV in Ontario, Canada. Participants were recruited through purposive sampling to reflect diverse lived experiences. An in-person, arts-based workshop included patient experience mapping, small group discussions, and creative artmaking to explore healthcare experiences and education priorities. Qualitative analysis was iteratively integrated into the co-design process, informing the development of a provider-facing educational pamphlet, which underwent iterative refinement based on feedback from participants and external primary care and geriatric providers.
Results:
Participants emphasized the need for long-term, HIV-informed care that affirms identity, fosters trust, and addresses fragmented care. Six core domains emerged as priorities for provider education: physical health, emotional health, mental health, social connection, spiritual well-being, and community support. Participants also highlighted the importance of addressing stigma, promoting cultural humility, and recognizing the cumulative impacts of aging with HIV. The final educational pamphlet used a circular, rainbow-themed design to reflect the interconnectedness of these domains and the diversity of the community. The resource was well-received by participants and external clinical reviewers for its clarity, relevance, and patient-centered approach.
Conclusions:
Co-designing education with older adults living with HIV resulted in a resource that reflects their lived experiences and care priorities. This approach demonstrates how participatory methods can bridge gaps between patient needs and provider practice.
Practice Implications:
This resource may improve provider awareness and empathy, inform training curricula, and promote inclusive care practices. Implementation in primary care settings is planned, along with future evaluation of its impact on provider knowledge and patient experience.
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