Evidence map›Paper›PMID 32760594›Full record

ArticleResearch involvement and engagement2020

Engaging indigenous patient partners in patient-oriented research: lessons from a one-year initiative.

Marie-Claude Tremblay, Maude Bradette-Laplante, Danielle Bérubé, Élaine Brière, Nicole Moisan, Daniel Niquay, Maman-Joyce Dogba, France Légaré, Alex McComber, Jonathan McGavock and 1 more

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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 · 2025
    Article
  5. Observational
  6. 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 · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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 · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Marie-Claude TremblayDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.ORCID 0000-0002-4965-2515
Maude Bradette-LaplanteDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Danielle BérubéDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Élaine BrièreDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Nicole MoisanDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Daniel NiquayDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Maman-Joyce DogbaDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
France LégaréDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.
Alex McComberDepartment of Family Medicine, Faculty of Medicine, McGill University, Montréal, Canada.
Jonathan McGavockDepartment of Pediatrics and Child Health, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Holly O WittemanDepartment of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Québec City, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AboriginalIndigenousMinority groupsPatient and public involvementPatient engagementResearch involvement

Identifiers

PMID32760594
PMCPMC7376932

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.