Gait Analysis in Neurological Disease
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Beth Israel Deaconess Medical Center
- Study ID
- NCT02994719
- Status
- Recruiting
Conditions
- Atypical Parkinson Disease
- Corticobasal Degeneration
- Gait, Frontal
- Huntington Disease
- Multiple System Atrophy
- Parkinson's Disease
- Parkinsonian Disorders
- Progressive Supranuclear Palsy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 85 Years
- Healthy Volunteers
- Accepted
Interventions
- Anti-Parkinson medication — DRUGDuring the optional second visit subjects with neurological disease and already on anti-parkinson medication are asked to come off their anti-parkinson medication.
- Deep Brain Stimulation — DEVICEDuring the optional second visit subjects with neurological disease already treated with deep brain stimulation are asked to come temporarily stop deep brain stimulation and resume stimulation, with walking trials done in each condition.
Study Details
The purpose of this study is to investigate whether speed-dependent measures of gait can be identified in patients with neurological conditions that affect gait, particularly in subjects with parkinsonian disorders.
Key Dates
- Start date
- Mar 1, 2016
- Status verified
- Jun 2025
- Primary completion
- Jun 20, 2026
- Completion
- Jun 20, 2026
Study Design
- Enrollment
- 120 participants (estimated)
Arms
- Arm: Neurological Disease subjectsParkinson's Disease and other Parkinsonian Disorders subjects. Other Parkinsonian Disorders include Atypical Parkinsonism such as Progressive Supranuclear Palsy, Multiple System Atrophy, Corticobasal Degeneration, Primary Gait Freezing Disorder, Indeterminate Parkinsonian Syndrome. During the first visit no intervention will take place. There is an optional second visit during which subjects with Parkinson's Disease are asked to come come off antiparkinson medication and if applicable, off both medication and deep brain stimulation.
- Arm: Healthy control subjectsThe healthy control subjects will be age- and sex-matched to the Neurological Disease subjects.
- Arm: Ataxia SubjectsThe ataxia subjects will participate in an additional cohort that will test and validate the gait model.
- Arm: Huntington Disease SubjectsThe Huntington Disease subjects will participate in an additional cohort that will test and validate the gait model.
Primary Outcome Measure
Gait speed [ Time Frame: through study completion, an average of 1 year ]
Central Contacts
- Veronique Vanderhorst, MD PhD617-667-0519
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Clinical Research Center BIDMC | Boston | Massachusetts | 02215 | - |
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