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Transnational Participation Research with Young Adults

Transnational Participatory Action Research with Young Adult Key Populations

This project promotes digital equity by empowering members from under-represented communities to co-produce data visualisations as a method to examine and challenge the impact of neutrality as a guiding principle in a particular and relevant case of digital good.

Team

Prof. Meg Davis
Centre for Interdisciplinary Methodologies, University of Warwick

Dr. Bernard Koomson
Centre for Interdisciplinary Methodologies, University of Warwick

Javier Garcia Martinez
Centre for Interdisciplinary Methodologies, University of Warwick

More information

DHRP Consortium

https://warwick.ac.uk/fac/cross_fac/cim/research/digital-health-rights/


https://warwick.ac.uk/fac/cross_fac/cim/research/digital-health-rights/publications/paying_costs_report_2025_digital.pdf

The Digital Helath and Rights Project (DHRP) consortium, Cape Town, South Africa

The project was inspired by the revolutionary impact of the global digital transformation and its consequence on health systems. While recent advancements in digital technologies have improved healthcare access in low- and middle-income countries (LMIC), socio-economic, gender and other inequalities create “digital divides”, and gaps in access that leave many without access to essential information and services. Moreover, efforts to regulate technology and online platforms have struggled to keep up with the pace of innovation, creating accountability concerns for growing youth populations. Working under the frame of participatory action research, the project explored the future of human rights in the digital age with young adult key populations in Colombia, Ghana, Kenya and Vietnam. Drawing on representatives from our study participants, we established Community Advisory Teams (CATs) in all four countries. The CATs, a unique component of our PAR framework, advised on the research design and recruitment of research participants, supported data collection and are currently leading on national advocacy plans. The study’s scope, the largest of its kind, highlights how barriers such as stigma, poor infrastructure, digital exclusion and online abuse are blocking access to essential health information and services online. We interviewed 301 young adults ages 18-30 who were either living with HIV and those categorised as key populations within HIV response such as sex workers, gay men and other men who have sex with men, transgender or gender diverse, or cisgender women. Additionally, weengaged 41 experts from UN agencies, government and civil society in Key Informant Interviews.

 

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