RECRUITING

Effects of Vibration on Motor Function of Survivors of Chronic Stroke

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 aim of this study is to evaluate how vibration of the tendons enhances arm and hand training in survivors of chronic stroke. The investigators hypothesize that wrist/elbow robotic training, combined with body awareness training will improve arm and hand function in individuals with chronic stroke.

Official Title

Effects of Vibration on Motor Function of Survivors of Chronic Stroke

Quick Facts

Study Start:2024-10-01
Study Completion:2027-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06663501

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:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * If stroke, more than 6 months after
  2. * Medically stable
  3. * Not currently taking any anti-spasticity medications (for at least 2 weeks)
  4. * Able to comply with study requirements
  1. * Recent change in the use of any medications
  2. * Other physical conditions such as orthopedic injuries or surgeries
  3. * Unstable Medical conditions or any other clinical observations that may affect the candidates performance, health, safety, or ability to participate in the study as determined by the treating therapist
  4. * Anti-spasticity drug injection in the 3 months prior to participation
  5. * Presence of significant cardiorespiratory or metabolic disease
  6. * Inability to achieve standard position required for EMG recordings
  7. * Intrathecal baclofen pump
  8. * Musculoskeletal conditions/surgeries resulting in difficulty participating
  9. * Adults unable to consent
  10. * Pregnant women, prisoners, and individuals under the age of 18

Contacts and Locations

Study Contact

Alexander J Barry, MS, CCRC
CONTACT
16309817670
alex.barry92@gmail.com

Principal Investigator

William Z Rymer, PhD
PRINCIPAL_INVESTIGATOR
Shirley Ryan AbilityLab

Study Locations (Sites)

Shirley Ryan AbilityLab
Chicago, Illinois, 60611
United States

Collaborators and Investigators

Sponsor: Shirley Ryan AbilityLab

  • William Z Rymer, PhD, PRINCIPAL_INVESTIGATOR, Shirley Ryan AbilityLab

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 Date2024-10-01
Study Completion Date2027-03-01

Study Record Updates

Study Start Date2024-10-01
Study Completion Date2027-03-01

Terms related to this study

Keywords Provided by Researchers

  • Upper extremity
  • AMES
  • Proprioception
  • Vibration

Additional Relevant MeSH Terms

  • Stroke
  • Healthy