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Not Yet Recruiting NCT07717528

Effect of Vestibular Rehabilitation on Gait, Balance, and Coordination in Post Concussion Combat Athletes

Conditions: Concussion Post Syndrome, Concussion

Sex: All
Ages: 18 Years – 30 Years
Healthy volunteers: No
Phase: NA
Enrollment: 44
Sponsor: Riphah International University

Location: Peshawar Sports Complex Peshawar Kpk

Summary

This randomized controlled trial aims to evaluate the effectiveness of vestibular rehabilitation in improving gait and balance among post-concussion combat athletes aged 18-25 years. Eligible participants diagnosed with mild traumatic brain injury and persistent post-concussion symptoms will be randomly assigned to either a vestibular rehabilitation group or a control group receiving conventional rehabilitation. Gait performance, balance, post-concussion symptom severity, and concussion severity will be assessed using the Timed Tandem Gait (TTG) Test, Balance Error Scoring System (BESS), Sport Concussion Office Assessment Tool 6 (SCOAT6), and Cantu Concussion Grading Scale. Outcome measures will be evaluated at baseline and after the 8-week intervention to determine the effectiveness of vestibular rehabilitation in enhancing functional recovery following concussion.

Eligibility Criteria

Inclusion Criteria: * Participants falling in this category would be recruited into the study. * Age 18-30 years. * Combat sport athletes (e.g, boxing, MMA, karate) with at least 2 years of training experience. * Experiencing post-concussion symptoms affecting gait, balance, or coordination * Willing and able to provide informed consent Exclusion Criteria: * Participants fall in this category would be excluded of the study. * History of moderate to severe TBI or repeated concussions (\>3 cantu scale) * Preexisting vestibular or neurological disorders unrelated to concussion (e.g., Meniere's disease, multiple sclerosis). * Current musculoskeletal injuries affecting gait or balance. * Visual or auditory impairments that interfere with assessments. * Use of medications that influence balance or coordination (e.g., sedatives, muscle relaxants). * Unwillingness or inability to participate in the full duration of the rehabilitation protocol.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07717528). StuddyBuddy aggregates publicly available trial information.