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

Health Expect. 2024 Feb;27(1):e13865. doi: 10.1111/hex.13865. Epub 2023 Sep 25.

Abstract

Introduction: The 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.

Methods: In 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.

Results: We 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.

Conclusions: We 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 contribution: This 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.

Keywords: co‐production; equity; knowledge mobilization; knowledge translation; research partnerships; research practices; research systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Community Participation / methods
  • Community-Based Participatory Research
  • Female
  • Health Services Research
  • Humans
  • Male
  • Middle Aged
  • Patient Participation
  • Research Design*