RECRUITING

Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation

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 purpose of this project is to compare a novel sensorimotor ankle rehabilitation training (SMART) protocol for Lateral ankle sprains (LASs) against a standard of care (SOC) protocol to determine if it is more successful at producing successful one-year outcomes and lower rates of re-injury and improved health. This will address the identified needs for evidence-support and reintegration strategies to improve understanding of the management of patient rehabilitation strategies throughout the rehabilitation process following neuromusculoskeletal injury. The project will validate an innovative rehabilitation approach while providing metrics of success using a variety of clinical and innovative markers.

Official Title

Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation

Quick Facts

Study Start:2019-11-12
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03663361

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 44 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * initiating rehabilitation for a first time acute grade I, II, or III LAS
  2. * have sustained within 72 hours of study enrollment
  3. * diagnosed by a physician, medic, athletic trainer, physical therapist, or other providing medical coverage in operational environments as having sustained a LAS
  1. * personal or familial history of epilepsy or seizures
  2. * history of migraine headaches
  3. * ocular foreign body, increased intracranial pressure, open head injury or significant closed head injury
  4. * cochlear implants
  5. * implanted brain stimulators, aneurysm clips or other metal in the head (except mouth)
  6. * implanted medication pumps, pacemakers or intracardiac lines
  7. * current medication with tricyclic anti-depressants, neuroleptic agents or other drugs that lower seizure threshold
  8. * history of diagnosed major psychiatric disorder
  9. * history of illicit drug use
  10. * current alcohol abuse or currently withdrawing from alcohol abuse
  11. * history of heart disease

Contacts and Locations

Study Contact

Kyle Kosik, PhD
CONTACT
859-323-9850
kyle.kosik@uky.edu

Principal Investigator

Phillip Gribble, PhD
PRINCIPAL_INVESTIGATOR
University of Kentucky

Study Locations (Sites)

University of Kentucky
Lexington, Kentucky, 40506
United States
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, 27599
United States

Collaborators and Investigators

Sponsor: Phillip Gribble

  • Phillip Gribble, PhD, PRINCIPAL_INVESTIGATOR, University of Kentucky

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 Date2019-11-12
Study Completion Date2025-12

Study Record Updates

Study Start Date2019-11-12
Study Completion Date2025-12

Terms related to this study

Keywords Provided by Researchers

  • ankle sprain, sensorimotor, rehabilitation, osteoarthritis

Additional Relevant MeSH Terms

  • Ankle Sprains