Recognizing patient partner contributions to health research: a mixed methods research protocol

Author:

Fox Grace,Fergusson Dean A.,Nicholls Stuart G.,Smith Maureen,Stacey Dawn,Lalu Manoj M.ORCID

Abstract

Abstract Background The overall aim of this program of research is to assess when/how patient partners are compensated financially for their contributions to health research. The research program consists of three studies to address the following questions: (1) What is the prevalence of reporting patient partner financial compensation? (2) What are researcher and institutional attitudes around patient partner financial compensation? (3) What are the current practices of patient partner financial compensation and what guidance exists to inform these practices? Methods In our first project, we will conduct a systematic review to assess the prevalence of reporting patient partner financial compensation and identify current financial compensation practices on an international scale. We will identify a cohort of published studies that have engaged patients as partners through a forward citation search of the Guidance for Reporting the Involvement of Patients and the Public (GRIPP I and II) checklists. We will extract details of financial compensation (type of financial compensation, amount, payment frequency etc.) and reported benefits, challenges, barriers and enablers to financially compensating patient partners. Quantitative data will be analyzed descriptively, and qualitative data will undergo thematic analysis. In our second project, we will conduct a cross-sectional survey of researchers who have engaged patient partners. We will also survey members of their affiliated institutions to gain further understanding of stakeholder experiences and attitudes with patient partner financial compensation. Survey responses will be analyzed by calculating prevalence. In our third project, we will conduct a scoping review to identify all published guidance and policy documents that guide patient partner financial compensation. Overton, the largest available online database of international policy documents, and the grey literature will be systematically searched. Data items will be extracted and presented descriptively. A comprehensive overview of guidance documents will be presented, which will represent a repository of resources that stakeholders can refer to when developing a financial compensation strategy. Discussion Our three studies will not only inform and assist patient partners and researchers by informing compensation strategies, but also support the inclusion of diverse perspectives. We will disseminate findings through traditional mediums (publications, conferences) as well as social media, non-technical summaries, and visual abstracts.

Funder

Ontario SPOR SUPPORT Unit

Publisher

Springer Science and Business Media LLC

Subject

General Health Professions,Health (social science)

Reference41 articles.

1. NIHR INVOLVE. Frequently asked questions: what is public involvement in research? https://www.nihr.ac.uk/health-and-care-professionals/engagement-and-participation-in-research/involve-patients.htm.

2. Canadian Institutes of Health Research. Strategy for patient-oriented research: patient engagement. 2019. https://cihr-irsc.gc.ca/e/45851.html.

3. PCORI. Glossary. https://www.pcori.org/glossary.

4. Duffett L. Patient engagement: what partnering with patient in research is all about. Thromb Res. 2017;150:113–20.

5. Aubin D, Hebert M, Eurich D. The importance of measuring the impact of patient-oriented research. CMAJ. 2019;191(31):E860–4.

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