Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation
Eligible age
18–44 yrs
Accepts
All genders
Locations
2 states
Healthy volunteers
No
See if you qualify for this study
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About this study
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.
Sponsor: Phillip Gribble
You may qualify if…
- ✓ 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
You may not qualify if…
- ✕ 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
- ✕ implanted brain stimulators, aneurysm clips or other metal in the head (except mouth)
- ✕ implanted medication pumps, pacemakers or intracardiac lines
- ✕ current medication with tricyclic anti-depressants, neuroleptic agents or other drugs that lower seizure threshold
- ✕ history of diagnosed major psychiatric disorder
Where it's recruiting
Lexington
Chapel Hill
Source: ClinicalTrials.gov · NCT03663361 · last updated 2026-02-20