Identifying potential barriers and solutions to patient partner compensation (payment) in research

Research Involvement and Engagement

Shoba Dawson¹  Laurie Proulx²  Dawn P. Richards³  Kelly D. Cobey⁴  Maarten de Wit⁵  Karine Toupin-April⁶ 

[1] Bristol Medical School, University of Bristol, Bristol, UK;Canadian Arthritis Patient Alliance, Ottawa, ON, Canada;Patient Research Partner, Ottawa, ON, Canada;Five02 Labs Inc, Toronto, ON, Canada;Canadian Institutes of Health Research Institute of Musculoskeletal Health and Arthritis, University of British Columbia, Vancouver, BC, Canada;Canadian Arthritis Patient Alliance, Ottawa, ON, Canada;Patient Research Partner, Toronto, ON, Canada;Meta-Research and Open Science Program, University of Ottawa Heart Institute, Ottawa, ON, Canada;School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada;Patient Research Partner, Zaltbommel, Netherlands;School of Rehabilitation Sciences, University of Ottawa, Ottawa, ON, Canada;Department of Pediatrics, University of Ottawa, Ottawa, ON, Canada;Children’s Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada;Institut du Savoir Montfort, Ottawa, ON, Canada;

关键词: Patient engagement;    Patient and public involvement;    Patient partner;    Patient research partner;    Payment;    Compensation;    Institutional barriers;    Barriers;   

DOI  :  10.1186/s40900-022-00341-1

来源: Springer

【 摘 要 】

Research that engages patients on the research team is often supported by grant funding from different organizations and, in some cases, principal investigators (who control the grant funding) provide patient partners with compensation (or payment) for their contributions. However, we have noted a gap in resources that identify and address barriers to compensating patient partners (no matter the size, degree or length of their engagement). In this paper, we present thoughts and experiences related to barriers to compensating patient partners with the goal of helping individuals identify and find solutions to these obstacles. Based on our experiences as individuals who live with chronic conditions and are patient partners, and those who are researchers who engage patient partners, we have identified eight barriers to compensating patient partners. We discuss each of these barriers: lack of awareness about patient partnership, institutional inflexibility, policy guidance from funders, compensation not prioritized in research budgets, leadership hesitancy to create a new system, culture of research teams, preconceived beliefs about the skills and abilities of patient partners, and expectations placed on patient partners. We demonstrate these barriers with real life examples and we offer some solutions. To further demonstrate these barriers, we ask readers to reflect on some scenarios that present realistic parallel situations to those that patient partners face. The intention is to illustrate, through empathy or putting yourself in someone else’s shoes, how we might all do better with respect to institutional barriers related to patient partner compensation. Last, we issue a call to action to share resources and identify actions to overcome these barriers from which we will create an online resource repository.

【 授权许可】

CC BY