Adaptive Portable Essential Tremor Monitor

Completed

• Conditions: Essential Tremor

• Registration Number: NCT01602042
• Lead Sponsor: Great Lakes NeuroTechnologies Inc.

Brief Summary

The purpose of this study is to evaluate the utility of a portable motion sensor-based system designed to monitor essential tremor (ET) to better prescribe therapy to minimize symptoms and expand care for ET patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-05
• Study First Submitted: 2012-05-16
• Study First Submitted QC: 2012-05-17
• Study First Posted: 2012-05-18
• Primary Completion: 2012-11
• Study Completion: 2012-11
• Status Verified: 2012-12
• Last Update Submitted: 2012-12-03
• Last Update Posted: 2012-12-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Aged 18 years or older
• Clinical diagnosis of essential tremor
• Able to provide informed consent

Exclusion Criteria

• Significant medical or psychiatric illness
• Not capable of following the required clinical instructions
• Serious medical conditions that compromise safety

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Tremor ratings during activities of daily living versus standardized tasks.	10 hours each day the sensor is worn.

Trial Locations

Locations (2)

Rush University Medical Center; 🇺🇸 Chicago, Illinois, United States

Baylor College of Medicine; 🇺🇸 Houston, Texas, United States