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Modifiable Variables in Parkinsonism (MVP)

StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Study title shortened, about 6 wordsv7
  2. Primary and study completion dates: Dec 2040 to Dec 2030
    • Site contact updated
    v6
  3. Primary and study completion dates: Dec 2019 to Dec 2040v5
  4. Re-verified, no change to tracked fieldsv4
  5. Primary and study completion dates: Aug 2017 to Dec 2019v3 Show 6 more changesShow less
    • Primary endpoints: 1 to 3
    • Eligibility criteria expanded, about 15 words
    • Secondary endpoint revised
    • Study description expanded, about 181 words
    • Site contact updated
    • Study title revised
  6. Study description expanded, about 71 wordsv2
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
We are trying to identify factors associated with improved quality of life and fewer PD symptoms. We are attempting to identify practices, beliefs, and therapies used by individuals who report excellent quality of life, few PD symptoms, and reduced rates of progression. After agreeing to participate, we will ask participants to fill our questionnaires about their experience with PD, their health in general, along with their food intake every six months for five years.
Trial Details
NCT Number NCT02194816
Lead Sponsor Bastyr University
Conditions
(from sponsor)		 Parkinson's Disease, Parkinsonism, MSA - Multiple System Atrophy, Progressive Supranuclear Palsy, Shy-Drager Syndrome, Corticobasal Degeneration, Dementia With Lewy Bodies, Pick Disease +1 more
Related terms Corticobasal Degeneration, Lewy Body Disease, Olivopontocerebellar Atrophies, Parkinson Disease, Parkinsonian Disorders, Pick Disease of the Brain, Shy-Drager Syndrome, Supranuclear Palsy, Progressive
Enrollment 2,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov