Adaptive Portable Essential Tremor Monitor

Phase II Study: Adaptive Portable Essential Tremor Monitor

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01602042

Enrollment

Registered

2012-05-18

Start date

2012-05-31

Completion date

2012-11-30

Last updated

2012-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential Tremor

Keywords

essential tremor, motion sensors, tremor

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

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

Countries

United States

Outcome results