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Tele-diagnostics for Remote Parkinson's Monitoring

G

Great Lakes NeuroTechnologies

Status

Completed

Conditions

Parkinson's Disease

Treatments

Device: Kinesia HomeView

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01356056
10-09-29-03EE
7R43NS065554-03 (U.S. NIH Grant/Contract)
5R43MD004049-02 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Enrollment

12 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Trial design

12 participants in 2 patient groups

Kinesia HomeView Monitoring
Description:
Uses Kinesia HomeView at home once per week
Treatment:
Device: Kinesia HomeView
Control
Description:
Assessed in the clinic every 4 weeks using traditional methods

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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