The Effects of Neuromuscular Training on Knee Biomechanics During Jump-Landing Among College Basketball Players Post ACL Reconstruction and Rehabilitation
1 other identifier
interventional
30
1 country
1
Brief Summary
Basketball players often injure the anterior cruciate ligament (ACL), a key structure that stabilizes the knee. Even after surgery and standard rehabilitation, many athletes continue to have problems with knee stability, movement control, and performance during jumping and landing. These issues increase the risk of re-injury and can limit their ability to return to competition. Neuromuscular training (NMT) is a type of exercise program that focuses on improving balance, muscle coordination, and movement patterns. It uses activities such as jump-landing drills, balance tasks, agility exercises, and core training. Previous research shows that NMT can help athletes land more safely, reduce harmful knee movements, and improve sport performance. However, little is known about its long-term benefits in college basketball players who are more than one year post-ACL surgery. This study aims to evaluate whether a 12-week NMT program, added to standard basketball training, can improve knee biomechanics, stability, and performance in college basketball players with a history of ACL reconstruction. Thirty participants will be randomly assigned to either an NMT group or a control group. Both groups will complete basketball training, but only the NMT group will receive the additional neuromuscular exercises. Knee movement will be measured using 3D motion capture and force plates, and performance will be tested through vertical jumps and other sport-specific tasks. The main outcomes will include knee angles during landing, ground reaction forces, dynamic stability, and jump height. The expected outcome is that athletes who undergo NMT will demonstrate safer landing strategies, better knee control, and improved performance compared to those who only receive standard basketball training. These findings may help coaches and healthcare providers design safer, more effective rehabilitation programs for athletes after ACL surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 10, 2025
CompletedFirst Submitted
Initial submission to the registry
December 15, 2025
CompletedFirst Posted
Study publicly available on registry
January 2, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 5, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
ExpectedJanuary 7, 2026
January 1, 2026
3 months
December 15, 2025
January 6, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Peak knee valgus angle during single-leg jump-landing (degrees)
Knee valgus angle will be measured using 3D motion capture during a standardized single-leg jump-landing task. The primary endpoint is the peak knee valgus angle (°) during the landing phase, averaged across 3 successful trials.
Baseline (pre-intervention) and 12 weeks (post-intervention)
Secondary Outcomes (8)
Time to stabilization after landing (seconds)
Baseline (pre-intervention) and 12 weeks (post-intervention)
Center of pressure displacement after landing, medial-lateral (millimeters)
Baseline (pre-intervention) and 12 weeks (post-intervention)
Peak knee flexion angle during single-leg jump-landing (degrees)
Baseline (pre-intervention) and 12 weeks (post-intervention)
Center of pressure displacement after landing, anterior-posterior (millimeters)
Baseline (pre-intervention) and 12 weeks (post-intervention)
Countermovement jump height (centimeters)
Baseline (pre-intervention) and 12 weeks (post-intervention)
- +3 more secondary outcomes
Other Outcomes (2)
Percentage of prescribed neuromuscular training (NMT) sessions completed
Throughout the 12-week intervention period
Number of participants with ≥1 intervention-related adverse event
Throughout the 12-week intervention period
Study Arms (2)
Neuromuscular Training (NMT) plus Standard Basketball Training
EXPERIMENTALParticipants in this arm will receive a 12-week neuromuscular training (NMT) program in addition to their regular basketball training. The NMT program will include balance tasks, jump-landing drills, agility exercises, and core strengthening. Sessions will be conducted in parallel with standard basketball practice.
Standard Basketball Training
NO INTERVENTIONParticipants in this arm will continue their usual basketball training program for 12 weeks without additional neuromuscular training. Training content and schedule will follow standard team practice routines. This arm will serve as a comparator to evaluate the added effect of NMT.
Interventions
The neuromuscular training (NMT) program is a 12-week behavioral intervention performed 2-3 times per week in addition to regular basketball training. It includes balance tasks, jump-landing drills, agility exercises, and core strengthening to improve knee stability and movement control after ACL reconstruction
Eligibility Criteria
You may qualify if:
- Age 18-25 years
- History of anterior cruciate ligament (ACL) reconstruction surgery at least 12 months before enrollment
- Cleared by physician for sports participation
- Willing to provide informed consent and comply with study procedures
You may not qualify if:
- Other major lower-limb injuries (e.g., meniscus, cartilage, fractures) in the past 12 months
- Current knee pain, swelling, or instability that prevents safe participation
- Neurological, cardiovascular, or systemic conditions that may affect training safety
- Participation in another structured neuromuscular training program within the past 6 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chengde Medical University, Affiliated Hospital
Chengde, Hebei, 067000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- This is an open-label study; both participants and investigators are aware of the intervention being administered.
- Purpose
- PREVENTION
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
December 15, 2025
First Posted
January 2, 2026
Study Start
December 10, 2025
Primary Completion
March 5, 2026
Study Completion (Estimated)
May 15, 2026
Last Updated
January 7, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, CSR