Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation

ConditionAnkle Sprains
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-44
SponsorPhillip Gribble

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

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Phillip Gribble

Lead sponsor

University of Kentucky

Sponsor institution

United States Department of Defense

Collaborator