About This Study
The purpose of this study is to gather information on people with Parkinson's disease through a patient registry. The registry will collect genetic information from people with Parkinson's, those at risk, and others without the disease. The registry will help improve understanding and care for Parkinson's disease.
What Activities Are a Part of this Study?
- Informed Consent Review
- Review of Medical History
- Phone Calls and/or Emails
- Study Visits and Consultations
- Surveys/Questionnaires
- Specimen Sample Collection
Age & Gender
- 18 - 100 years old
- All Genders
Language
- This study enrolls English speakers only
Additional Study Information
- No compensation provided
- No reimbursement offered
Study Locations
- Greater Charlotte, NC