Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
250 participants
OBSERVATIONAL
2004-05-31
2020-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Neurological Injury
No interventions assigned to this group
No Neurological Injury
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* patients: neurological movement disorder
Exclusion Criteria
* presence of any central psychiatric disorder that precludes subject from giving informed and voluntary consent
* presence of any cardiovascular conditions or limitations that restrict the ability to walk on a treadmill continuously for more than 20 minutes
* for the electrical stimulation examination, subjects with metal implants are also excluded
* for the TMS and GVS examination, subjects with the following conditions are excluded: metal implants in the head, cardiac pacemakers, history of migraine headaches, history of major head injury, history of stroke, history of seizures, previous brain neurosurgery, unstable medical conditions, major psychiatric disorders, pregnancy -
18 Years
ALL
Yes
Sponsors
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University of Zurich
OTHER
Responsible Party
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Locations
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University of Zurich
Zurich, , Switzerland
Countries
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Other Identifiers
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EK-11/2004 / PB_2016-00229
Identifier Type: -
Identifier Source: org_study_id
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