Plain-English translation of NCT04496973 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Parkinson Disease research guide →The University of Delaware is building a registry of people with Parkinson's disease who want to help advance research. By joining, you agree to share your contact information and basic health details so researchers can invite you to participate in future studies about topics like brain changes, balance, gait, and how exercise affects movement in Parkinson's disease.
Parkinson's disease affects more people every year, and researchers need participants to help test new ideas and treatments. Finding enough willing volunteers is one of the biggest challenges in moving this research forward, so this registry makes it easier to connect people with Parkinson's disease to studies that need them.
You likely qualify if…
You likely don't qualify if…
Joining this registry involves providing your contact information and some basic medical information about your Parkinson's disease diagnosis. Once you're enrolled, researchers at the University of Delaware will contact you when they have studies available that match your health profile, and you can decide whether to participate in each one.
AI-generated summary from trial data · Jun 10, 2026 · Not medical advice
United States
Enrollment target
~1,000 participants
Started
May 2020
Primary completion
January 2030
Age range
21 Years – 100 Years
Last updated on clinicaltrials.gov in May 2024.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Roxana Burciu, PhD
University of Delaware
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.