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Clinical Trials/NCT01356056
NCT01356056
Completed
Not Applicable

Tele-diagnostics for Remote Parkinson's Monitoring

Great Lakes NeuroTechnologies Inc.1 site in 1 country12 target enrollmentMay 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson's Disease
Sponsor
Great Lakes NeuroTechnologies Inc.
Enrollment
12
Locations
1
Primary Endpoint
UPDRS
Status
Completed
Last Updated
13 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
December 2011
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

UPDRS

Time Frame: Every 4 weeks

PDQ-39

Time Frame: Every 4 weeks

Study Sites (1)

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