Skip to main content
Clinical Trials/NCT01648803
NCT01648803
Completed
N/A

Wearable Movement Sensors for Assessing Motor Impairments and Dyskinesias in Parkinson Disease

University of Rochester1 site in 1 country12 target enrollmentJanuary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
University of Rochester
Enrollment
12
Locations
1
Primary Endpoint
1-3Hz gyroscope signal power
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to measure motor fluctuations and dyskinesias in patients with Parkinson's disease using movement sensors (accelerometers and gyroscopes) to determine if this is a feasible measure to use in addition to self report, and eventually the goal will be to replace self report with a more reliable measure such as movement sensors.

Detailed Description

Patients with Parkinson disease and motor fluctuations will wear movement sensors during their regular clinic visit with the principal investigator. The visit will be videotaped and medication status (ON without dyskinesia, ON with dyskinesia, or OFF) will be independently rated from review of the video.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
June 2013
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participants who will be included in the study have probable or definite idiopathic PD (CAPSIT criteria (23)), Hoehn \& Yahr stage 2-4;
  • One or more of the following PD-associated motor impairments experienced in the week prior to enrollment (based on history and/or examination): motor fluctuations (end of dose wearing off with hypokinesia and/or levodopa-induced choreiform dyskinesias), tremor, freezing of gait, or frequent falls (≥ 1 per week).

Exclusion Criteria

  • Neurological disorders (other than PD) or orthopedic deficits that, in the investigator's judgement, contribute substantially to impaired movement (e.g. stroke with motor sequelae;
  • Essential tremor;
  • Severe osteoarthritis);
  • Cognitive impairment sufficiently severe to interfere with informed consent.

Outcomes

Primary Outcomes

1-3Hz gyroscope signal power

Time Frame: 30 second windows spanning the observation period

Study Sites (1)

Loading locations...

Similar Trials