"Nothing About Us, without Us." How Community-Based Participatory Research Methods Were Adapted in an Indigenous End-of-Life Study Using Previously Collected Data

被引:23
作者
Funnell, Sarah [1 ]
Tanuseputro, Peter [2 ]
Letendre, Angeline [3 ]
Bearskin, Lisa Bourque [4 ]
Walker, Jennifer [5 ]
机构
[1] Queens Univ, Dept Family Med, Haynes Hall 3rd Floor,115 Clarence St, Kingston, ON K7L 5N6, Canada
[2] Univ Ottawa, Bruyere Res Inst, Ottawa, ON, Canada
[3] Alberta Hlth Serv, Populat Publ & Indigenous Hlth, Edmonton, AB, Canada
[4] Tompson Rivers Univ, Sch Nursing, Kamloops, BC, Canada
[5] Laurentian Univ, Sch Rural & Northern Hlth, Sudbury, ON, Canada
来源
CANADIAN JOURNAL ON AGING-REVUE CANADIENNE DU VIEILLISSEMENT | 2020年 / 39卷 / 02期
关键词
aging; Indigenous; First Nation; Inuit; Metis; routinely collected data; previously collected data; health administrative data; community-based participatory research methods; research ethics; NATIONS; HOME;
D O I
10.1017/S0714980819000291
中图分类号
R4 [临床医学]; R592 [老年病学];
学科分类号
1002 ; 100203 ; 100602 ;
摘要
Indigenous health research in Canada has a chequered past and has been identified as problematic and lacking in appropriate collaboration with Indigenous people. The Tri-Council Policy Statement on Ethical Conduct for Research Involving Humans, Chapter 9 describes ethical conduct of research regarding First Nations, Inuit, and Metis Peoples. First Nations Ownership, Control, Access, and Possession (OCAP (R)) Principles highlight the necessity of Indigenous engagement and governance. To ensure that the aims and activities of the research being developed are in full and meaningful partnership with Indigenous peoples and communities, community-based participatory research (CBPR) methods provide a process in which full engagement is possible. Research utilizing secondary data sets, such as routinely collected health administrative data, should no longer be excluded from this approach. Our aim was to describe how our research team of academic researchers and a national Indigenous health organization adapted CBPR methods in a research project using previously collected data to examine end-of-life health care service delivery gaps for Indigenous people in Ontario. We describe the process of how we developed our research partnership and how grounding principles and Indigenous ways of knowing guided our work together. Through the adaptation of CBPR methods, our research partnership illustrates a process of engagement that can guide others hoping to conduct Indigenous health research using previously collected data. We also present a transparent research agreement negotiated equally by a national Indigenous health organization and research scientists, which can also be used as a framework for others wishing to establish similar research partnerships. Ensuring that Indigenous perspectives are central to and reflected in the research process is essential when using health administrative data.
引用
收藏
页码:145 / 155
页数:11
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