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AIDS 2026: Defining Indigenous Data Sovereignty as a Determinant of Health

Clinical Thought

At AIDS 2026, I found myself pondering a deceptively simple question: Who governs knowledge about Indigenous peoples? For decades, Indigenous peoples in Canada have participated in HIV research, yet have not been given a voice in research planning, analyses, or decision-making. Here, I discuss why I believe Indigenous data sovereignty must be understood as a determinant of health, rather than just a research ethics issue. 

Released: September 14, 2026

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Provided by

Provided by Clinical Care Options, LLC dba Decera Clinical Education in partnership with the International AIDS Society.

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Supporters

This activity is supported through independent educational grants from Gilead Sciences, Inc., Merck & Co., Inc., Rahway, NJ, USA, and ViiV Healthcare.

Gilead Sciences, Inc.

Merck & Co., Inc., Rahway, NJ, USA

ViiV Healthcare

Partners

International AIDS Society

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Target Audience

This activity is intended for physicians, pharmacists, registered nurses, and other healthcare professionals who care for people living with or at risk of HIV infection.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Appropriately apply and counsel patients regarding the clinical role(s) of new and investigational ART regimens and strategies

  • Devise HIV management strategies based on the results of recent clinical studies of established antiretroviral agents

  • Integrate the latest scientific findings to develop and optimize effective HIV prevention interventions

Financial Disclosures

Primary Author

Randall Jackson, PhD, has no relevant financial relationships to disclose.