Neuromuscular Intervention Targeted to Mechanisms of ACL Load in Female Athletes
Rehabilitation, ACL Reconstruction

About this trial
This is an interventional treatment trial for Rehabilitation focused on measuring ACL Reconstruction, Rehabilitation, Sports Injury, Neuromuscular Intervention, Knee Injury
Eligibility Criteria
Inclusion Criteria:
- Age, 13 ≥ 30 years
- Acute (< 6 months), first-time, isolated ACL injury
- No history of previous knee surgery to either extremity
- No low back or lower extremity injury in the year prior to ACL injury necessitating medical care
- Pre-injury participation in cutting, jumping or pivoting sports for ≥ 50 hours/year
- Mechanism of injury did not involve a direct blow to the knee.
- Patients who sustain a medial collateral ligament (MCL) injury are eligible for study participation if medial knee instability is resolved prior to surgery
- Patients with simple meniscus tears (i.e., 2 cm vertical longitudinal tear) that do not necessitate alterations in rehabilitation will be eligible for study participation
Exclusion Criteria:
- History of previous knee surgery to either extremity
- Low back or lower extremity injury in the year prior to ACL injury necessitating medical care
- Second or greater ACL injury
- Greater than 6 months since occurrence of ACL injury
- Lack of participation in cutting, jumping, or pivoting sport
- Mechanisms of injury involved a direct blow of force to the knee
- Patients with MCL injury that exhibits unresolved medial knee instability
- Patients with complex, repairable meniscus tears (i.e., radial or root repair) and patients with full thickness articular cartilage lesions will not be eligible for participation secondary to significant alterations to postoperative rehabilitation protocol
Sites / Locations
- Mayo Clinic SquareRecruiting
- Mayo Clinic in RochesterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Other
Experimental
STAN
HOME
TNMT
Patients in the STAN group will participate in twelve sessions of supervised physical therapy over a six week period. Patients will participate in agility and plyometric drills, and continue strength exercises from the previous treatment phase. The clinic program will be performed in conjunction with a home running program. Patients in this group will not receive feedback from the therapist regarding movement quality during activities.
HOME Program is distinguished by patients participating in a home only intervention that consists of running and strengthening exercises performed twice a week for six weeks. No plyometric or agility drills are performed in this study arm. This represents the minimal intervention to prepare for a return to sports. No neuromuscular training or movement training beyond the sagittal plane will be performed.
Patients who are enrolled in the TNMT group will participate in 12 sessions of supervised outpatient physical therapy over a six week period. The TNMT protocol is distinguished by performance of exercises designed to enhance core and hip strength, performance of neuromuscular training exercise that are designed to correct movement flaws associated with second ACL injury25, providing verbal and visual feedback and performance of single leg drills on both legs.