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NCT01602042 Clinical Trial

Adaptive Portable Essential Tremor Monitor

Essential Tremor Clinical Trial

Official title:
Phase II Study: Adaptive Portable Essential Tremor Monitor

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01602042
Other study ID # 2R44AG034708-02A1
Secondary ID
Status Completed
Phase N/A
First received May 16, 2012
Last updated December 3, 2012
Start date May 2012
Est. completion date November 2012

Study information
Verified date December 2012
Source Great Lakes NeuroTechnologies Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date November 2012
Est. primary completion date November 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Rush University Medical Center Chicago Illinois
United States Baylor College of Medicine Houston Texas

Sponsors (4)
Lead Sponsor Collaborator
Great Lakes NeuroTechnologies Inc. Baylor College of Medicine, National Institute on Aging (NIA), Rush University Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Tremor ratings during activities of daily living versus standardized tasks. 10 hours each day the sensor is worn. No
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