A Study of Neurophysiologic Changes in Individuals With Parkinson's Disease

NCT00117195 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 620

Last updated 2012-02-09

No results posted yet for this study

Summary

The goal of this study is to investigate neurophysiologic tests that have the potential of serving as screening tools for Parkinson's disease. These neurophysiologic tests will be administered to individuals with Parkinson's disease and parkinsonian syndrome and validated against a healthy control population.

Specifically, this study will look at changes in motor function, cognitive function, handwriting, speech, and olfactory function in individuals with Parkinson's disease, individuals at risk for Parkinson's disease and healthy controls.

Conditions

Interventions

DEVICE

Automated Neuropsychological Assessment Matrix

This study will evaluate a profile of neurophysiologic tests for potentially predictive signs of PD or PS in individuals with PD or PS, those who may be at risk for PD or PS and in a population of individuals without parkinsonian symptoms or any other neurologic conditions. In addition, the study will evaluate serum samples for changes in proteins or metabolites that may be indicators of early changes associated with Parkinson's disease or parkinsonian syndrome.

Sponsors & Collaborators

  • Molecular NeuroImaging

    collaborator OTHER
  • Institute for Neurodegenerative Disorders

    lead OTHER

Principal Investigators

  • Kenneth L Marek, MD · Institute for Neurodegenerative Disorders

  • Laura Leary · Institute for Neurodegenerative Disorders

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-05-31
Primary Completion
2011-01-31
Completion
2012-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00117195 on ClinicalTrials.gov