Abstract
Background
Involving collaborators and partners in research may increase relevance and uptake, while reducing health and social inequities. Collaborators and partners include people and groups interested in health research: health care providers, patients and caregivers, payers of health research, payers of health services, publishers, policymakers, researchers, product makers, program managers, and the public. Evidence syntheses inform decisions about health care services, treatments, and practice, which ultimately affect health outcomes.
Our objectives are to:
A. Identify, map, and synthesize qualitative and quantitative findings related to engagement in evidence syntheses
B. Explore how engagement in evidence synthesis promotes health equity
C. Develop equity-oriented guidance on methods for conducting, evaluating, and reporting engagement in evidence syntheses
Methods
Our diverse, international team will develop guidance for engagement with collaborators and partners throughout multiple sequential steps using an integrated knowledge translation approach:
1. Reviews. We will co-produce 1 scoping review, 3 systematic reviews and 1 evidence map focusing on (a) methods, (b) barriers and facilitators, (c) conflict of interest considerations, (d) impacts, and (e) equity considerations of engagement in evidence synthesis.
2. Methods study, interviews, and survey. We will contextualise the findings of step 1 by assessing a sample of evidence syntheses reporting on engagement with collaborators and partners and through conducting interviews with collaborators and partners who have been involved in producing evidence syntheses. We will use these findings to develop draft guidance checklists and will assess agreement with each item through an international survey.
3. Consensus. The guidance checklists will be co-produced and finalised at a consensus meeting with collaborators and partners.
4. Dissemination. We will develop a dissemination plan with our collaborators and partners and work collaboratively to improve adoption of our guidance by key organizations.
Conclusion
Our international team will develop guidance for collaborator and partner engagement in health care evidence syntheses. Incorporating partnership values and expectations may result in better uptake, potentially reducing health inequities.
Involving collaborators and partners in research may increase relevance and uptake, while reducing health and social inequities. Collaborators and partners include people and groups interested in health research: health care providers, patients and caregivers, payers of health research, payers of health services, publishers, policymakers, researchers, product makers, program managers, and the public. Evidence syntheses inform decisions about health care services, treatments, and practice, which ultimately affect health outcomes.
Our objectives are to:
A. Identify, map, and synthesize qualitative and quantitative findings related to engagement in evidence syntheses
B. Explore how engagement in evidence synthesis promotes health equity
C. Develop equity-oriented guidance on methods for conducting, evaluating, and reporting engagement in evidence syntheses
Methods
Our diverse, international team will develop guidance for engagement with collaborators and partners throughout multiple sequential steps using an integrated knowledge translation approach:
1. Reviews. We will co-produce 1 scoping review, 3 systematic reviews and 1 evidence map focusing on (a) methods, (b) barriers and facilitators, (c) conflict of interest considerations, (d) impacts, and (e) equity considerations of engagement in evidence synthesis.
2. Methods study, interviews, and survey. We will contextualise the findings of step 1 by assessing a sample of evidence syntheses reporting on engagement with collaborators and partners and through conducting interviews with collaborators and partners who have been involved in producing evidence syntheses. We will use these findings to develop draft guidance checklists and will assess agreement with each item through an international survey.
3. Consensus. The guidance checklists will be co-produced and finalised at a consensus meeting with collaborators and partners.
4. Dissemination. We will develop a dissemination plan with our collaborators and partners and work collaboratively to improve adoption of our guidance by key organizations.
Conclusion
Our international team will develop guidance for collaborator and partner engagement in health care evidence syntheses. Incorporating partnership values and expectations may result in better uptake, potentially reducing health inequities.
Original language | English |
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Article number | 134 |
Journal | Systematic Reviews |
Volume | 12 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2 Aug 2023 |
Bibliographical note
Funding Information:The authors are grateful to Maureen Smith, Elise Berliner, and Neal Haddaway for their contributions to the research grant proposal.
Publisher Copyright:
© 2023, The Author(s).