Relational practices for meaningful inclusion in health research: Results of a deliberative dialogue study

Author:

Plamondon Katrina1ORCID,Banner Davina2ORCID,Cary Miranda A.3,Faulkner Melissa1,Gainforth Heather4,Ghag Kiranpreet2,Hoens Alison5,Huisken Anne1,Kandola Damanpreet K.2,Khan Shaheer1,Silva Aline Silveira1,Oelke Nelly16,Rai Ashmita1,Strain Kimberly7,Sibley Kathryn M.89,Wick Ursula10

Affiliation:

1. Faculty of Health and Social Development School of Nursing, University of British Columbia Kelowna British Columbia Canada

2. Faculty of Human and Health Sciences School of Nursing, University of Northern British Columbia Prince George British Columbia Canada

3. Research and Knowledge Translation in Long Term Care Vancouver Island Health Victoria British Columbia Canada

4. Faculty of Health and Social Development School of Health and Exercise Sciences, University of British Columbia Kelowna British Columbia Canada

5. Department of Physical Therapy University of British Columbia Vancouver British Columbia Canada

6. Rural Coordination Centre of BC Vancouver British Columbia Canada

7. BC SUPPORT Unit Fraser Centre Abbotsford British Columbia Canada

8. Department of Community Health Sciences University of Manitoba Winnipeg Manitoba Canada

9. Knowledge Translation George and Fay Yee Centre for Healthcare Innovation, Rady Faculty of Health Sciences Winnipeg Manitoba Canada

10. Facets Holistic Self‐Discovery Toronto Ontario Canada

Abstract

AbstractIntroductionThe importance of including people affected by research (e.g., community members, citizens or patient partners) is increasingly recognized across the breadth of institutions involved in connecting research with action. Yet, the increasing rhetoric of inclusion remains situated in research systems that tend to reward traditional dissemination and uphold power dynamics in ways that centre particular (privileged) voices over others. In research explicitly interested in doing research with those most affected by the issue or outcomes, research teams need to know how to advance meaningful inclusion. This study focused on listening to voices often excluded from research processes to understand what meaningful inclusion looks and feels like, and asked what contributes to being or feeling tokenized.MethodsIn this deliberative dialogue study, 16 participants with experience of navigating social exclusions and contributing to research activities reflected on what makes for meaningful experiences of inclusion. Using a co‐production approach, with a diversely representative research team of 15 that included patient and community partners, we used critically reflective dialogue to guide an inclusive process to study design and implementation, from conceptualization of research questions through to writing.ResultsWe heard that: research practices, partnerships and systems all contribute to experiences of inclusion or exclusion; the insufficiency or absence of standards for accountability amplifies the experience of exclusion; and inclusive practices require intention, planning, reflection and resources.ConclusionsWe offer evidence‐informed recommendations for the deeply relational work and practices for inclusivity, focused on promising practices for cultivating welcoming systems, spaces and relationships.Patient or Public ContributionThis work reflects a co‐production approach, where people who use and are affected by research results actively partnered in the research process, including study design, data‐generating activities, analysis and interpretation, and writing. Several of these partners are authors of this manuscript.

Publisher

Wiley

Subject

Public Health, Environmental and Occupational Health

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