Education & Training

The Parkinson’s Foundation and Parkinson Study Group have partnered on patient engagement in research design and implementation for ten years. As part of this partnership, we are pleased to provide training resources for study coordinators.

Our first resource contains three videos:

Research Education
1. An introductory video to the research process
2. An overview of patient engagement in research
3. An introductory video to our patient engagement in research work

Stay tuned for more resources on how research is conducted. By the end of this year, the Parkinson’s Foundation will launch a free, open access, online course covering topics including information on ethics and informed consent, analyzing and interpreting research and recruiting representative populations into research.Patient Engagement in Research.

Learn more about the Parkinson’s Foundation’s patient engagement in research program here. Our methodology of patient engagement can be found here. Examples of our Research Advocacy program work on bringing in representative populations to research can be found here and here. To join our efforts, contact Karlin Schroeder, Associate Vice President, Community Engagement, kschroeder@parkinson.org or (646) 388-7641.

THE RESEARCH PROCESS VIDEOS

More videos coming soon!

Patient Engagement in Research
Community Based Research
Patient Engagement in Research
Ethics

ADDITIONAL EDUCATION & TRAINING RESOURCES

Download this presentation here.
The Research Clinic Simulation
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Chicago Movement Coalition Website