or this study, by “patient partner” we mean patients, clients, family members, and caregivers who are working to improve the health system by drawing on their experiences. /3
1
6
Welcome to the Public and Patient Engagement Collaborative
.jpeg?sfvrsn=8d18da3b_0&MaxWidth=800&MaxHeight=699&ScaleUp=false&Quality=High&Method=ResizeFitToAreaArguments&Signature=CB98D8134EFD0D1646D19183180A9D4200AC6520)
The Public and Patient Engagement (PPE) Collaborative was established in 2011. Our research and service activities focus on the role of patients and publics in health system policy making and health research, with a specific focus on the evaluation of these efforts.
This website has been designed as a portal to access the latest research and news from the PPE Collaborative and to share tools for use in practice. Please use the links above to learn more about the PPE Collaborative.
You can also get updates about the PPE Collaborative's work on Twitter.
News and Updates
Calling all Patient Partners and Advisors! The Canadian Patient Partner Study (CPPS) Survey is now available. The purpose of this survey is to learn more about who Canadian patient partners are, what they do, the challenges they face and how best to support them. To complete the survey, or for more information, please follow the following links: http://bit.ly/CPPS_ECPP (English survey), or http://bit.ly/ECPP_CPPS (French survey)
Julia was a recent guest on Jennifer Johannesen and Emily Nicholas Angl's Matters of Engagement podcast where she discussed evaluating patient engagement and her experiences as a researcher of patient engagement who also partners with patients. You can listen to the podcast here.
An updated version of the Public and Patient Engagement Evaluation Tool (PPEET) was released in 2018. For more information and to download the tool, please see the PPEET page on this site.