ArticleResearch involvement and engagement2020
Engaging indigenous patient partners in patient-oriented research: lessons from a one-year initiative.
Article in Research involvement and engagement, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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Who cites it
18 citing papers in PubMed.
- Compensating patient partners on health research teams: a qualitative descriptive study of barriers, facilitators, and implications for equity, diversity, and inclusion in Canadian patient-oriented research.Research involvement and engagement · 2026Article
- Using a co-design approach to develop aquatic reactive balance training for fall prevention.PloS one · 2026Article
- "Inclusivity requires an active effort": building an inclusive and diverse space when engaging people with lived and living experience and caregivers in mental health and substance use health research.Research involvement and engagement · 2025Article
- The Importance of Lived Experience: A Scoping Review on the Value of Patient and Public Involvement in Health Research.Health expectations : an international journal of public participation in health care and health policy · 2025Article
- An Evaluation of Racial and Ethnic Representation in Research Conducted with Young Adults Diagnosed with Cancer: Challenges and Considerations for Building More Equitable and Inclusive Research Practices.Current oncology (Toronto, Ont.) · 2024Observational
- What guidance exists to support patient partner compensation practices? A scoping review of available policies and guidelines.Health expectations : an international journal of public participation in health care and health policy · 2024Article
- Article
- Doing community-based research during dual public health emergencies (COVID and overdose).Harm reduction journal · 2023Article
- Working together in health research: a mixed-methods patient engagement evaluation.Research involvement and engagement · 2023Article
- Engaging diverse patients in a diverse world: the development and preliminary evaluation of educational modules to support diversity in patient engagement research.Research involvement and engagement · 2023Article
- Roles, outcomes, and enablers within research partnerships: A rapid review of the literature on patient and public involvement and engagement in health research.Research involvement and engagement · 2023Review
- Co-Design of an Intervention to Increase the Participation in Leisure Activities Including Adolescents with Cerebral Palsy with GMFCS Levels IV and V: A Study Protocol.Journal of clinical medicine · 2022Article
- Patient, family member and caregiver engagement in shaping policy for primary health care teams in three Canadian Provinces.Health expectations : an international journal of public participation in health care and health policy · 2022Article
- Inter-individual relationships within a Canadian SPOR research network: a social network study.BMC health services research · 2022Article
- Lessons learned developing and deploying a provincial virtual mental health support during the COVID-19 pandemic.Healthcare management forum · 2022Article
- The impacts of partnering with cancer patients in palliative care research: a systematic review and meta-synthesis.Palliative care and social practice · 2022Review
- Missing Persons Alert: Finding the Lost "Person" in Patient-Oriented Research.Journal of patient experience · 2022Article
- Patient complexity assessment tools containing inquiry domains important for Indigenous patient care: A scoping review.PloS one · 2022Article
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPatient-oriented research (POR) is a specific application of participatory research that promotes active patient engagement in health research. There is a growing concern that people involved in POR do not reflect the diversity of the population such research aims to serve, but are rather those more 'easily' engaged with institutions, organizations and society. Indigenous peoples are among such groups generally underrepresented in POR. The "Indigenous patient partners platform project" was a small-scale initiative aimed to address the issue of the underrepresentation of Indigenous people in patient-oriented research by recruiting, orienting and supporting Indigenous patient partners in Québec (Canada). This article reports on the findings of an evaluation conducted at the end of the project to garner lessons and identify strategies for engaging Indigenous patient partners in patient-oriented research.
methodsThe evaluation of this initiative used a case study design hinging on documentary analysis and committee member interviews. Project documents (
resultsResults point to four key components of Indigenous patient partner engagement in POR: initiation of partnership, interest development, capacity building and involvement in research. Specific lessons emphasize the importance of community connections in recruiting, sustaining and motivating patient partners, the need to be flexible in the engagement process, and the importance of consistently valuing patient partner contributions and involvement.
conclusionsThere is a need to engage Indigenous patient partners in POR to ensure that healthcare practices, policies and research take their particular needs, stories and culture into account. While results of this evaluation are generally consistent with the existing literature on patient engagement, they offer additional insight into how to effectively engage Indigenous patient partners in research, which might also be relevant to the involvement of other marginalized populations who have been historically and systemically disempowered.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.