Plain-English translation of NCT05066763 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Parkinson Disease research guide →The Parkinson's Foundation wants to hear directly from people affected by Parkinson's disease—whether you have the condition, care for someone who does, or work with patients as a healthcare professional. By answering periodic surveys, you'll help researchers understand what life is really like living with this disease and what support matters most.
Parkinson's disease affects millions of people, but researchers don't always understand the full picture of how it impacts daily life, relationships, and healthcare needs. This survey initiative fills that gap by collecting real experiences from the people who know best.
You likely qualify if…
You likely don't qualify if…
You'll receive periodic surveys from the Parkinson's Foundation asking about your experiences, challenges, and needs related to Parkinson's disease. There are no medications to take or medical procedures involved—just answering questions in your own time, either online or by other methods the foundation offers. The foundation may also reach out about other research opportunities in the future.
AI-generated summary from trial data · Jul 10, 2026 · Not medical advice
United States
Enrollment target
~1,000,000 participants
Started
April 2021
Primary completion
December 2030
Age range
18 Years and older
Last updated on clinicaltrials.gov in October 2021.
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.