About this trial
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.
Eligibility criteria
Qualifiers
initiating rehabilitation for a first time acute grade I, II, or III LAS
have sustained within 72 hours of study enrollment
diagnosed by a physician, medic, athletic trainer, physical therapist, or other providing medical coverage in operational environments as having sustained a LAS
Disqualifiers
personal or familial history of epilepsy or seizures
history of migraine headaches
ocular foreign body, increased intracranial pressure, open head injury or significant closed head injury
cochlear implants
Trial design
Treatments tested in this trial
- SMART Intervention
- Standard of Care Intervention
Treatment groups
Sponsors and collaborators
Phillip Gribble
Lead sponsor
University of Kentucky
Sponsor institution
United States Department of Defense
Collaborator