Joining our secure registry does not require you to participate in any study. It simply gives us permission to contact you with information about research opportunities that match your basic info; you decide if and when you would like to take part. You are unlikely to be contacted more than a handful of times per year, and you can pause or halt this at any time.

Enrolling in the registry takes just a few minutes and can be done from your smartphone, tablet, or computer. You will be asked to complete a consent form and a brief health survey to help us find the best matches for you. 

Please note that we are looking for people both with and without movement disorders to participate in our studies. If you have any questions, contact the movement disorders research team at studyvolunteer@umn.edu.

Every treatment available to patients today exists because someone like you chose to participate in research. By joining this registry, you can help us find the treatments of tomorrow, and bring us closer to a cure.

If you would like other ways to support Parkinson’s research at UMN, consider making a tax-deductible donation.

Thank you for your support!