RecruitingNot ApplicableNCT06257069

Tremor Retrainer Software Application for Functional Tremor


Sponsor

University of Virginia

Enrollment

20 participants

Start Date

Jan 17, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this clinical trial is to learn about the Tremor Retrainer smartphone application and Simplified Functional Movement Disorder Rating Scale in patients with functional tremor. The main questions the study aims to answer are: 1. Is the Tremor Retrainer application usable for patients and are there signs that it can help functional tremor? 2. Can a televideo administration of the Simplified Functional Movement Disorder Rating Scale give enough information to use this scale via televideo in future studies?


Eligibility

Min Age: 10 Years

Inclusion Criteria5

  • Age 10 years and older, any gender, any race
  • Functional tremor as defined by Espay and Lang25, diagnosed by a movement disorders neurologist, involving at least 1 arm and ongoing at time of enrollment.
  • Access to internet and a laptop or tablet with a videocamera.
  • Informed consent obtained and signed
  • Subject understands study procedures and is able to comply with study procedures for duration of study

Exclusion Criteria4

  • Parkinson's disease, essential tremor, or other disorders causing involuntary movements in addition to functional tremor
  • Cognitive impairment with previously diagnosed intellectual disability (IQ<70) or dementia
  • Hearing impairment not addressed by hearing aids
  • Prior enrollment in clinical trial involving the Tremor Retrainer application

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICETremor Retrainer Smartphone Application

The Tremor Retrainer smartphone application uses the smartphone's built-in accelerometer to calculate a patient's tremor frequency when the smartphone is strapped to the patient's wrist. The application will provide auditory cues to the patient with a treatment frequency at 2/3 the patient's baseline tremor frequency for half a session, then 1/3 the patient's baseline tremor frequency for the second half of the session. Meanwhile, oscillatory movements will be continuously analyzed with frequency calculated and displayed relative to goal frequency, so that the patient receives continuous feedback via a visual dial as to whether they are meeting treatment goals. Intervention will consist of a one-week Tremor Retrainment Protocol.


Locations(1)

University of Virginia

Charlottesville, Virginia, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06257069


Related Trials