Damage-centred research has been defined as "a persistent trend in research on Native communities, city communities, and other disenfranchised communities" wherein research is consistently focussed on exposing all the ways in which the community is "broken" (Tuck, E. Cited in Transformative Research Toolkit) - with the ultimate result of defining entire communities and their members in terms of their economic, social and health-related disadvantages.
"With their limited scope, aggregate format, deficit focus and decontextualized framework this... (research) narrative cannot, and does not, yield meaningful portraits of...Indigenous lives (Walter M. & Russo, S. in Indigenous Data Sovereignty & Policy). |
"Decolonizing research is a process whereby Eurocentric views and methods are decentred and dismantled....Indigenizing research is a process for conducting research with Indigenous communities that places Indigenous voices and epistemologies at the centre of the research process and deliberately works against colonial norms" (Simonds et al, as cited by Hayward et al. Addressing the Need for Indigenous and Decolonized Quantitative Research Methods in Canada). |
An unfortunate reality to grapple with when searching for materials that were created in the past is the offensive/problematic terminology that may have been used to denote Indigenous, racialized and/or vulnerable people.
"Finding data on race, racialized populations, and anti-racism in Canada can be a complex process when conducting research....(as) the collection of racial, ethnic, or Indigenous data has changed throughout the years and from Census to Census" (Manuel, K., Orlandini, R., & Cooper, A., Who is counted? Ethno-racial and Indigenous identities in the Census of Canada, 1871-2021).
"Existing principles within the open data movement (e.g. FAIR: findable, accessible, interoperable, reusable) primarily focus on characteristics of data that will facilitate increased data sharing among entities while ignoring power differentials and historical contexts. The emphasis on greater data sharing alone creates a tension for Indigenous Peoples who are also asserting greater control over the application and use of Indigenous data and Indigenous Knowledge for collective benefit" (Global Indigenous Data Alliance. CARE Principles for Indigenous Data Governance). |
"Data sovereignty refers to a group or individual’s right to control and maintain their own data, which includes the collection, storage, and interpretation of data.
Indigenous data sovereignty refers to the ability for Indigenous peoples to control their data and includes autonomy regarding a variety of data types such as oral traditionals (sic), DNA/genomics, community health data, etc" (National Library of Medicine. Data Sovereignty).
To Learn More See:
First Nations Information Governance Centre (FNIGC) - The First Nations Principles of OCAP®
Global Indigenous Data Alliance - to learn more about the international CARE Principals of Collective benefit, Authority to control, Responsibility & Ethics
The following have been developed by various Indigenous communities - local and global - to guide researchers in ensuring that Indigenous Peoples benefit from the data derived from their participation in research projects. It's important to note, however, that none of these principles have been developed as a generic approach. Each community is distinct, and has different customs and protocols for working with external researchers, so researchers should approach new communities with this in mind. |
Traditional Knowledge Labels are used by Indigenous communities to make clear how their traditional knowledge may be accessed and/or used by others in ways that are consistent with "existing community rules, governance and protocols for using, sharing and circulating knowledge and data."
The CARE Principles for Indigenous Data Governance are designed to complement the FAIR principles and take into account the current and historic power imbalances between researchers and Indigenous communities. CARE stands for:
See the Global Indigenous Data Alliance web site to learn more about the CARE Principals.
See also: GIDA's Indigenous Peoples' Rights in Data
The OCAP® Principles of data governance outline how to interact with First Nations data. OCAP® stands for:
OCAP® certifications are available through the First Nations Information Governance Centre (FNIGC). OCAP® is a registered trademark of the FNIGC.
Negotiating Research Relationships with Inuit Communities: from the Inuit Tapiriit Kanatami and Nunavut Research Institute, this is an online guide for researchers (PDF).
Principles of Ethical Métis Research: from the National Aboriginal Health Organization (NAHO), this is an online guide for researchers (PDF).
Addressing the Need for Indigenous and Decolonized Quantitative Research Methods in Canada. (Hayward, A. et al). https://doi.org/10.1016/j.ssmph.2021.100899
BC First Nations' Data Governance Initiative (BCFNDGI)
First Nations Information Governance Centre (FNIGC)
Indigenous Data Governance: Indigenous Research Support Initiative (IRSI)
Indigenous Data Sovereignty and Data Justice in the Age of AI [podcast 50:36]: Centre for Health Innovation, Queen's University
Indigenous Data Sovereignty and Policy. [e-Book]. (Walter, M, Kukutai, T., Russo Carrol, S., & Rodriguez-Lonebear, D.)
Indigenous Research (SHHRC)
Strengths-Based Approaches to Indigenous Research and the Development of Well-Being Indicators. [PDF]. (FNIGC Research Series).