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- IMMPACT-XXV Slide Presentations
- 1. Definitions, historical perspective and best practices on patient engagement in research
- Christine Goertz, DC, PhD
- 2. Major findings of background scoping/narrative review
- Simon Haroutounian, PhD, MSc
- 3. Major findings of systematic review
- Ewan McNicol, PharmD, MS, and McKenzie Ferguson, PharmD
- 4. Research agency funders panel discussion
- 4a. David Atkins, MD, MPH
- 4b. Rebecca Baker, PhD
- 4c. Kristin Carman, PhD, MA
- 4d. Rachel Knowles, MD, PhD
- 4e. Jeremy Taylor, OBE
- 5. The "how tos:" starting at the beginning - how to identify, locate, and incorporate patients in the planning of clinical pain research
- Karen Morales, BS, and Gail Graham
- 6. Special considerations: inclusion of diverse, disparate and hard to reach populations
- Jonathan Jackson, PhD
- 7. The "how tos:" incorporating patient partners in the conduct of clinical pain research
- Kathryn Martin, PhD, MPH, and Lynn Laidlaw
- 8. The "how tos:" incorporating patient partners in the dissemination/implementation of findings from clinical pain research
- Christine Chambers, PhD, and Isabel Jordan, BSc
- 9. The "how tos:" special considerations for industry pain trials
- David Leventhal, MBA
- 10. Regulatory agency perspectives in engaging patient partners and other stakeholders in the planning and conduct of pain clinical trials
- 10a. Nathalie Bere, MPH
- 10b. Robyn Bent, RN, MS, CAPT
- 10c. Alysha Croker, PhD
- 11. The "how tos:" measuring patient engagement in the planning, conduct and dissemination/implementation of clinical pain research
- Laura Forsythe, PhD, MPH
- 12. Journal reporting on patient (and other stakeholder) engagement in the planning and conduct of clinical pain research
- 12a. Frank Keefe, PhD
- 12b. Mark Jensen, PhD