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University of Delaware Parkinson's Disease Registry

University of Delaware Participant Recruitment Registry for Parkinson's Disease Research

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04496973
Enrollment
1000
Registered
2020-08-04
Start date
2020-05-28
Completion date
2030-01-01
Last updated
2024-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

Parkinson's Disease

Brief summary

The purpose of this Parkinson's Disease Registry is to assist with recruitment of willing participants into future Parkinson's disease research studies at the University of Delaware.

Detailed description

There is an urgent need for Parkinson's Disease research due to its increasing global prevalence. Participant recruitment is a significant challenge to the success of Parkinson's disease research and we need your help more than ever in moving the field forward and improving the lives of people who have Parkinson's disease. Recruitment of study participants can be facilitated by maintaining registries of people who agree to be contacted for future studies. The purpose of the University of Delaware Participant Recruitment Registry for Parkinson's Disease Research is to create a registry that includes the contact information and basic health information pertaining the participant's diagnosis of Parkinson's disease. The registry will streamline recruitment and enrollment in a variety of research studies focusing on topics such as, but not limited to: brain changes in Parkinson's disease, balance and gait in Parkinson's disease, exercise and its effect on motor function. To be in the registry individuals must have a clinical diagnosis of Parkinson's Disease and have an interest in participating in research studies. To become a member of this registry, primary information including contact information and some general medical information are needed.

Interventions

None listed

Sponsors

University of Delaware
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Individual 21 years old or older * A clinical diagnosis of Parkinson's disease * Interest in participating in one or more investigator-led research studies at the University of Delaware

Exclusion criteria

* Individuals with a clinical diagnosis of parkinsonism that is not considered primary (e.g. vascular parkinsonism) or an atypical parkinsonian syndrome (e.g., progressive supranuclear palsy, multiple system atrophy, corticobasal degeneration etc.) * Clinical diagnosis of dementia

Design outcomes

Primary

MeasureTime frameDescription
Parkinson's Disease DiagnosisOnce a year, at the beginning of the yearBy following up once a year, we will evaluate a participant's medical history to validate a diagnosis of Parkinson's Disease. A confirmed diagnosis of Parkinson's Disease is a criteria for continuing to be a part of the registry.

Countries

United States

Contacts

Primary ContactRoxana Burciu, PhD
rgburciu@udel.edu302-831-3066

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026