Parkinson's Disease and Movement Disorders Clinical Database
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- University of Pennsylvania
- Enrollment
- 250
- Locations
- 1
- Primary Endpoint
- Genetic and Neurobiological factors
Study Overview
Brief Summary
The research database contains demographic and family history information, longitudinal information on the clinical symptoms, neuropsychological profile and treatments, stored biological samples, and brain images of patients with Parkinson's disease and related disorders receiving care at the Parkinson's disease and Movement Disorders Center and the Hospital of the University of Pennsylvania.
Detailed Description
The research database contains demographic and family history information, longitudinal information on the clinical symptoms, neuropsychological profile and treatments, stored biological samples, and brain images of patients with Parkinson's disease and related disorders receiving care at the Parkinson's disease and Movement Disorders Center (PDMDC) and the Hospital of the University of Pennsylvania.
The purpose of the research database is to have a comprehensive source of data that can be used for educational, research and patient care projects at the PDMDC. These data may be used for any study examining the relationship between treatment and clinical symptoms of patients with PD and related disorders. The main uses of the data are to:
- Determine the long term effects of Parkinson's disease and related conditions, including predictors of its motor and non-motor symptoms
- Identify genetic and other neurobiological factors related to the risk of developing Parkinson's disease and related disorders and their course
- Improve our understanding of how best to identify, diagnose, and manage motor and non-motor symptoms of Parkinson's disease and related conditions Evaluate biological markers of disease or response to therapy
- Identify patients who may be candidates for participation in trials of new medications.
- Identify patients who may be interested in participating in educational or developmental activities
Participants are seen annually for the first 4 years, biennially thereafter. The participants continue in the study until study end, withdrawal, or death on study.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Other
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Any person who receives medical care for the diagnosis of Parkinson's disease with mild cognitive impairment (MCI) or dementia may be eligible to participate in the research database. There are no limitations for database participation based on age, disease severity or presence of cognitive impairments, as long as the person is able to complete the research assessments.
Exclusion Criteria
- •Absence of Parkinson's disease diagnosis. There are no limitations for database participation based on age, disease severity or presence of cognitive impairments, as long as the person is able to complete the research assessments.
Outcomes
Primary Outcomes
Genetic and Neurobiological factors
Time Frame: 5 years
Identify genetic and other neurobiological factors related to the risk of developing Parkinson's disease and related disorders and their course
Long term effects of Parkinson's disease
Time Frame: 5 years
Determine the long term effects of Parkinson's disease and related conditions, including predictors of its motor and non-motor symptoms
Secondary Outcomes
- Identification and Diagnosis of Parkinson's disease(5 years)
Investigators
Daniel Weintraub
Professor of Psychiatry and Neurology
University of Pennsylvania