Patient Engagement in Cancer Research Community of Practice
Welcome to the Community of Practice
Patient engagement is a crucial part of meaningful cancer research but has been siloed across Canada. Recognizing that many patient engagement initiatives exist, the Patient Engagement in Cancer Research Community of Practice was developed to break down these silos by:
- Building relationships and connections with others involved in patient engagement
- Developing and harnessing patient engagement resources
- Facilitating cross-organizational collaborations
The overall mission of the Community of Practice is to embed and optimize patient engagement in cancer research in Canada.
A Short History
Judy Needham, a person with lived experience, had the idea to bring people together and in 2022 the Community of Practice was started by 8 people including researchers, people with lived experience and administrators. Community of Practice development included the establishment of Executive Sponsorship and a Secretariat for support provided by CCS, a Steering Committee, the development of a Terms of Reference and a call for membership.
After inviting people from across Canada, the first Community of Practice meeting was held in April 2022.What is a Community of Practice?
Why host a Community of Practice?
What you can expect
As of 2024, there are more than 70 members in the Community of Practice from more than 45 organizations. People have many different backgrounds including lived experience, researchers, clinicians, research funders, trial sponsors, research networks, not for profits, and industry. Seven provinces and more than 20 cities are represented. Growing the diversity of the Community of Practice is one focus of the group.
The Community of Practice currently includes: @(Model.HeadingTag)>
A LinkedIn group for networking, communication, resource and event sharing between meetings
If you have an interest in patient engagement in cancer research and are based in Canada, you can join the group below
Topics Previously Covered | Year |
Engaging patients in clinical trials |
2022 |
Online learning modules for patient engagement |
2022 |
Future directions for patient-oriented research |
2023 |
Equity, diversity and inclusion in patient engagement |
2023 |
Patient-centered approach to clinical trials |
2023 |
Patient engagement in cancer clinical trials |
2023 |
Patient engagement in basic science research |
2024 |
Patient research prioritization |
2024 |
Indigenous patient engagement |
2024 |
How to join @(Model.HeadingTag)>
Acknowledgements
Steering Committee (2024)
- Jennifer Wilson, CCS
- Stephanie Michaud, BioCanRx
- Judy Needham, CCTG
- Stephen Sundquist, 3CTN
- Don Wood
- Meera Rayar, UBC
- Sevtap Savas, Memorial University
- Justin Noble, OICR
Secretariat
- Don Wood
- Judit Takacs (Maternity Leave)
Founders
- Judy Needham, CCTG
- Jennifer Wilson, CCS
- Stephen Sundquist, 3CTN
- Kim Badovinac, CCRA
- Robin Urquhart, Dalhousie University
- Stephanie Michaud, BioCanRx
- Antonia Palmer, Kindred Foundation
- Patrick Sullivan