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Patient Engagement Resources
Clinical trials would not be possible without the active engagement of the public, patients, patient partners, communications professionals, and community partners. Below are available resources to address training needs of community members.
ACT Canada Resources:
- The ACT Patient Engagement Committee hosted a panel discussion in June 2024 on common patient engagement misconceptions.
- In January 2025, ACT hosted a webinar by Maureen Smith and Andrea Chow titled:
“Engaging patient partners in your CIHR grant application: Everything you ever wanted to know” - In Fall 2024, the ACT Patient Engagement Committee collaborated with the ACT Training Committee to develop a collection of patient engagement resources for ACT members.
Additional Resources:
- In March 2025, a member of the Pewaseskwan Indigenous Wellness Research Group presented to the SUPPORT Unit Council on ethical practices for Indigenous engagement in clinical trials with a focus on self-determination, data sovereignty, and the incorporation of traditional knowledge in research.
