RECRUITING

Vibrotactile Stimulation for Upper-Extremity Stroke Rehabilitation

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to investigate upper-extremity vibrotactile stimulation with wearables in stroke patients. The main questions it aims to answer are: Are the wearables well-tolerated by patients? Does the vibrotactile stimulation help regain arm function? Participants will wear vibrotactile stimulation gloves and shirts for 5 hours daily during their stay at the rehabilitation unit, in addition to conventional therapy. Researchers will compare the treatment group (vibrotactile stimulation wearables) with a control group (conventional therapy only) to see the effects of the vibrotactile stimulation.

Official Title

Vibrotactile Stimulation for Neurological Disorders

Quick Facts

Study Start:2024-02-02
Study Completion:2025-02-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06244719

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:50 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Inpatients at rehabilitation units
  2. * Unilateral left or right sided ischemic stroke within the previous 2 weeks
  3. * Have Upper-Extremity Fugl-Meyer scores between 6 and 58
  4. * Have at least 20 degrees of active shoulder elevation and elbow flexion
  5. * Expected to stay 1-3 weeks in the rehabilitation unit
  1. * Under anti-spasticity therapy
  2. * Patients that are dependent on pacemakers
  3. * Patients that have defibrillators
  4. * Have lymphedema or AV fistula for dialysis on an arm

Contacts and Locations

Study Contact

Mazen Al Borno, PhD
CONTACT
303-315-1408
mazen.alborno@ucdenver.edu

Study Locations (Sites)

UCHealth Rehabilitation Unit
Aurora, Colorado, 80045
United States
Broomfield Hospital
Broomfield, Colorado, 80021
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-02
Study Completion Date2025-02-02

Study Record Updates

Study Start Date2024-02-02
Study Completion Date2025-02-02

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke