Supplementary Neuromuscular Rehabilitation During Acute Concussion Recovery
Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-24
SponsorNorthern Illinois University
About this trial
Approximately 1.6 to 3.8 million mild traumatic brain injuries, or concussions, occur yearly in the United States. Although most individuals progress through return-to-activity (RTA) using symptom-guided aerobic and functional activity, current protocols do not directly target neuromuscular deficits linked to persistent movement alterations after concussion. These deficits include altered gait, reduced movement efficiency, and biomechanical changes that persist beyond symptom resolution and increase subsequent risk of musculoskeletal injury. This creates a critical clinical gap: patients are cleared using symptom-tolerance protocols, while concussion-related neuromuscular impairments remain untreated during the period when recovery behaviors are established. The proposed project addresses this gap by testing a low-cost, equipment-free neuromuscular rehabilitation strategy added to standard RTA during acute concussion recovery. The intervention applies the six principles of clinical Pilates, concentration, control, centering, precision, flow, and breathing, through ten therapeutic movements designed to improve posture, flexibility, balance, strength, muscle control, body awareness, and movement confidence.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
aged 18 to 24 years old
be a registered member of an intercollegiate sports team
have received a medically confirmed concussion within 7 days of the initial study visit.
Disqualifiers
moderate or severe traumatic brain injury
red-flag signs or symptoms requiring urgent medical evaluation
current lower-extremity injury that prevents safe walking or therapeutic exercise
a neurological or vestibular disorder unrelated to concussion that independently affects balance or gait
Trial design
Design model
Parallel
Treatments tested in this trial
Exercise
BehavioralThe intervention will include 10 standardized exercises: pelvic tilts, bridging, seated spinal twists, bent-knee fallouts, supine toe taps, clamshells, side-lying leg lifts, supine side-to-sides, quadruped arm and leg reach, and standing roll downs. Not every exercise will be performed during every session. Exercise selection will follow a prespecified intervention framework designed to provide consistent exposure to the major movement domains of the protocol while permitting symptom-guided modification. The standardized protocol will identify the exercises eligible for each stage of progression and the criteria required to advance to more demanding movements. Research personnel will select exercises from the appropriate stage based on the participant's current tolerance, symptom response, movement quality, and prior session performance.
Return to Activity Progression
BehavioralA research team member will attend each RTA session to collect symptom ratings immediately before and after the session. Assessments will occur whenever the athlete completes an RTA session, up to five days per week, between days 7 and 35 after concussion. These repeated observations will characterize symptom response to standard RTA throughout recovery.
Treatment groups
30 Participants
are divided into 2 treatment groupsGroup A: Supplementary Neuromuscular RehabilitationExperimental treatment 1 intervention
Group B: Standard Return to ActivityActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
Symptom Burden
Symptom Burdent
Time frame
Day 7 to 352
Tandem Gait Performance
Tandem Gait time to complete
Time frame
Day 7 to 353
Recovery Time
Time to Recovery
Time frame
Day 7 to 35Sponsors and contacts
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Source ClinicalTrials.gov
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