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
12 participants
OBSERVATIONAL
2011-05-31
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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Kinesia HomeView Monitoring
Uses Kinesia HomeView at home once per week
Kinesia HomeView
Quantifies motor symptom severity in the home
Control
Assessed in the clinic every 4 weeks using traditional methods
No interventions assigned to this group
Interventions
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Kinesia HomeView
Quantifies motor symptom severity in the home
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Subjects with cognitive impairments that would prohibit them from properly using the Kinesia HomeView system
* Subjects without the cognitive ability to respond to researchers and let them know when any parameters of the study may become uncomfortable
* Subjects found on examination by our clinicians to have any physical limitations which would be counter productive to participation in this study.
ALL
No
Sponsors
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University of Cincinnati
OTHER
Great Lakes NeuroTechnologies Inc.
INDUSTRY
Responsible Party
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Locations
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University of Cincinnati
Cincinnati, Ohio, United States
Countries
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Other Identifiers
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