Patient EngagEment in Research
The Patient EngagEment in Research (PEER) webinar series was a joint initiative from the Chronic Pain Network's Patient Engagement, Training & Mentoring and Knowledge Translation committees.
The webinars, geared towards trainees, addressed a multitude of subjects, including What is Patient Engagement and Patient Oriented Research - A Patient Perspective; Plain Language Summaries and Knowledge Translation; and An Introduction to Working with Indigenous Communities - just to name a few. The series launched in July 2020, with new webinars taking place each month. Webinars were recorded and can be viewed on the Chronic Pain Network's YouTube channel or below.
An Introduction to Patient Engagement in Research
De-Mystifying Patient Engagement in Research: A Collaborative Journey
Bringing Patient Engagement in Health Research and Knowledge Translation Together
Patient Engagement in Basic Science Projects: A Case Study
The fourth webinar in the PEER series, hosted by Richard Hovey and Therese Lane,
features guests Nader Ghasemlou and Lesley Singer.
Navigating Knowledge about Protocols and Conducting Indigenous Health Research
Lived Experience of Chronic Pain in the Work of the Canadian Pain Task Force
Jacques Laliberté, Linda Wilhelm and other members of the Canadian Pain Task Force
discuss how people with lived experience are helping to shape government policy through
their valuable contributions.
Innovative Ways of Mobilizing Knowledge with and for Patients
Engagement is Key! SKIP: A Patients-Included Approach to Knowledge Mobilization
The team from Solutions for Kids in Pain (SKIP) discuss how patients and the patients-included
approach can enhance knowledge mobilization, as well as research as a whole.
Learn more about skip at:
Annual Report: https://www.kidsinpain.ca/annual-reports