Tele-diagnostics for Remote Parkinson's Monitoring
Completed
- Conditions
- Parkinson's Disease
- Interventions
- Device: Kinesia HomeView
- Registration Number
- NCT01356056
- Lead Sponsor
- Great Lakes NeuroTechnologies Inc.
- Brief Summary
The purpose of this research study is to design, implement, and clinically assess a portable, user worn system for monitoring Parkinson's disease (PD) motor symptoms. The current standard in evaluating symptoms is the Unified Parkinson's Disease Rating Scale (UPDRS), a subjective, qualitative ranking system. The main goal of this research is to develop a quantitative system, Kinesia HomeView, to assess tremor as well as different features of bradykinesia in a home based system which can capture those symptom changes over the course of a day and aid in evaluating treatment protocol efficacy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 12
Inclusion Criteria
- Clinical diagnosis of Parkinson's disease
Exclusion Criteria
- Inability to follow the required clinical instruction
- 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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Kinesia HomeView Monitoring Kinesia HomeView Uses Kinesia HomeView at home once per week
- Primary Outcome Measures
Name Time Method UPDRS Every 4 weeks PDQ-39 Every 4 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Cincinnati
🇺🇸Cincinnati, Ohio, United States