Our Publications

A curated collection of Digital Health and Rights Project peer-reviewed journal articles, reports, policy briefs, and more for in-depth exploration.

Meaningful Participation of Young Adults and Civil Society in Digital Governance Consultations: Research Brief

Digital Health and Rights Project Consortium + et al

This research brief shares findings from a study with 50 young adults and civil society leaders from Colombia, Ghana, Kenya and Vietnam who advocated for digital rights in local, national, regional and global consultations to explore what they experienced as meaningful in their participation.

A Rights-Based Approach to the WHO Global Strategy on Digital Health 2028-2033: Policy Brief

Sara L.M. Davis

This brief draws on a review of human rights standards and peer-reviewed studies of digital health strategies
to recommend steps to wire human rights into digital health by design: Set clear objectives to spur action to address human rights harms; Build on existing UN human rights standards
and platforms; and Promote greater accountability, including meaningful participation of young people and civil society in digital health governance.

The Future of Human Rights in the Digital Age: Kenya Policy Brief

Olendo Obondo + et al

This policy brief summarises recommendations from a study conducted by the Digital Health and Rights Project (DHRP)10 in Kenya (led in Kenya by the Kenya Legal and Ethical Issues Network on HIV and AIDS (KELIN) and University of Warwick).

The study, part of a four-country transnational participatory action research project, examined how young people living with HIV (PLHIV), young female sex workers,
and young LGBTQ+ individuals navigate digital spaces, focusing on empowerment, inclusion, and governance from a human rights perspective. The policy brief, led by KELIN, shares evidence-based recommendations for Kenya.

National Policy Brief – Navigating Human Rights and Risks Online: Young Ghanaians and the Future of Digital Health

Digital Health and Rights Project

This national policy brief examines how young people in Ghana navigate digital spaces to access health information, with a focus on human rights and exposure to online risks. Drawing on participatory research, it highlights experiences of online harms and abuse, misinformation, and privacy concerns affecting young key populations. It finds that marginalised young adults face significant economic barriers, particularly the high cost of mobile devices and internet data, limiting access. Stigma related to health status, gender identity, and occupation further discourages engagement. These intersecting risks deepen exclusion, underscoring the need for inclusive, rights-based digital health policies that ensure safe, affordable, and equitable access.

Defining Digital Health: Recommended Definitions on Digital Health and Human Rights for Policy-Makers

Cindy Marcela Zapata + et al

Language matters, and how we define digital health can shape how we experience it. However, digital health stakeholders often define key terms in different ways. This can result in difficulties when policy-making, as deciding to use one definition may exclude others and therefore the varied experiences and understandings of the subject.