ArticleHealth promotion international2026
Promoting self-determined Indigenous data governance in Canada: the Métis Health Research and Data Governance Principles.
Article in Health promotion international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
5 authors.
Funding
Abstract
Population-level data collection is crucial to advance Indigenous rights and sovereignty but requires localized approaches to develop representative datasets. In Canada, a focus on First Nations research and data governance and principles has led to the underrepresentation of Métis realities and a reliance on data governance models that fail to address their unique cultural, historical, and community-specific needs. "The Saskatchewan Métis Health Research and Data Governance Principles©" were developed to guide Métis research and promote Métis data sovereignty. While these principles share similarities with the First Nations Principles of OCAP®, they emphasize Métis-specific priorities such as capacity building and active engagement with Métis rights holders. These principles provide a framework for Métis health research, ensuring that Métis values and perspectives are embedded throughout the research lifecycle.
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Registered trials
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