Noninterventional Study Evaluating Parkinson's Disease Diary Use (NCT05363046)
A Multi-center, Noninterventional Study Evaluating Variability, Reliability, and Compliance for the Parkinson's Disease Diary
🩺 Plain-English Summary (8th-Grade Level)
This study aims to evaluate the impact of the frequency of assessments on the variability over time, reliability, and compliance for the Parkinson's disease (PD) diary in patients with PD in whom medications do not provide adequate control of symptoms.
Who can join: Review the eligibility criteria below.
Location: Mayo Clinic Neurology — Scottsdale, Arizona
Age range: 39 Years to 70 Years
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (34 Sites)
Showing the first 25 of 34 sites.
- Mayo Clinic Neurology — Scottsdale, Arizona
- David Geffen School of Medicine University of California Los Angeles — Los Angeles, California
- University of California, Irvine — Orange, California
- University of Colorado — Aurora, Colorado
- Movement Disorders Center of Boca Raton — Boca Raton, Florida
- University of Miami Health System — Miami, Florida
- Parkinson's Disease and Movement Disorders Center at Northwestern University Feinberg School of Medicine — Chicago, Illinois
- University of Kansas Medical Center — Kansas City, Kansas
- University of Louisville — Louisville, Kentucky
- Tufts Medical Center — Boston, Massachusetts
- Mount Sinai West — New York, New York
- Weill Cornell Medicine - New York Presbyterian Hospital — New York, New York
- University of Rochester Medical Center — Rochester, New York
- Cleveland Clinic — Cleveland, Ohio
- Vanderbilt University Medical Center — Nashville, Tennessee
- Evergreen Health Medical Center — Kirkland, Washington
- Toronto Western Hospital — Toronto, Ontario
- Dkd Wiesbaden — Wolfach, Baden-Wurttemberg
- Klinikum der Universität München - Campus Grosshadern — Munich, Bavaria
- Technischen Universitaet Muenchen (TUM) — Munich, Bavaria
- Universitätsklinikum Würzburg - Medizinische Klinik — Würzburg, Bavaria
- Klinik und Poliklinik für Neurologie am Standort Marburg — Marburg, Hesse
- Universitaetsklinikum Duesseldorf AöR — Düsseldorf,
- Universitätsmedizin Rostock — Rostock,
- University Hospital Tuebingen — Tübingen,
📞 Contact the Study Coordinator
Phone: (800) 664-4580
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.