Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1000 participants
OBSERVATIONAL
2020-05-28
2030-01-01
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* 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
* Clinical diagnosis of dementia
21 Years
100 Years
ALL
No
Sponsors
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University of Delaware
OTHER
Responsible Party
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Roxana Burciu
Roxana Burciu, PhD
Locations
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University of Delaware
Newark, Delaware, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1535874
Identifier Type: -
Identifier Source: org_study_id
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