Risk Factors for Progressive Supranuclear Palsy (PSP)

Sponsor
University of Louisville (Other)
Overall Status
Completed
CT.gov ID
NCT00431301
Collaborator
National Institute on Aging (NIA) (NIH)
942
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82
94.2
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Study Details

Study Description

Brief Summary

Progressive supranuclear palsy (PSP) is the most common atypical parkinsonian movement disorder. This study will determine the role of specific genetic, occupational and environmental components in the development of PSP by evaluating patients with this disorder and age and gender matched controls.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This proposal will determine: (1) if there is an association between PSP and specific genes of interest; (2) if there is an association between PSP and occupational and/or environmental chemical exposures functionally or structurally similar to known parkinsonian toxicants; and (3) if hypertension or traumatic brain injury prior to symptom-onset is associated with PSP. To disentangle the complex etiology of PSP, this case-control multicenter study involves 500 PSP cases, 500 age/gender matched primary controls, and 500 secondary controls for genetic confirmation. Understanding the etiology of PSP may also help explain the causes of other related diseases such as Alzheimer's disease. This multidisciplinary team of movement disorder specialists, epidemiologists, geneticists, biostatisticians, industrial hygienist and toxicologist is well suited to unravel the etiology of PSP.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    942 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Genetic and Environmental Risk Factors for PSP
    Study Start Date :
    Aug 1, 2006
    Actual Primary Completion Date :
    Feb 1, 2013
    Actual Study Completion Date :
    Jun 1, 2013

    Arms and Interventions

    Arm Intervention/Treatment
    Case

    PSP Cases

    Control

    Healthy Controls

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      40 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • PSP patients able to visit one of the screening sites for diagnostic confirmation and able to participate in a one hour telephone interview
      Exclusion Criteria:
      • No other major neurological disorders

      • Unable to communicate by telephone

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 University of Alabama, Birmingham Birmingham Alabama United States 35233
      2 UCLA Los Angeles California United States 90095-1759
      3 University of Colorado Aurora Colorado United States 80045
      4 Emory College of Medicine Atlanta Georgia United States 30322
      5 Rush University Chicago Illinois United States 60611
      6 University of Kansas Kansas City Kansas United States 66160
      7 University of Louisville Louisville Kentucky United States 40202
      8 University of Maryland Baltimore Maryland United States 21201
      9 Case Western University Cleveland Ohio United States 44106
      10 University of Toronto Toronto Ontario Canada M5T 2S8

      Sponsors and Collaborators

      • University of Louisville
      • National Institute on Aging (NIA)

      Investigators

      • Principal Investigator: Irene Litvan, M.D., University of Louisville

      Study Documents (Full-Text)

      None provided.

      More Information

      Additional Information:

      Publications

      None provided.
      Responsible Party:
      University of Louisville
      ClinicalTrials.gov Identifier:
      NCT00431301
      Other Study ID Numbers:
      • 1R01AG024040-01A2
      • 1R01AG024040-01A2
      First Posted:
      Feb 5, 2007
      Last Update Posted:
      Apr 10, 2017
      Last Verified:
      Apr 1, 2017

      Study Results

      No Results Posted as of Apr 10, 2017