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The Impact of Accelerated Rehabilitation Program Based on Enhanced ACL Reconstruction on Return-to-sport Time, Function and Graft Outcomes in Patients

The Impact of Accelerated Rehabilitation Program Based on Enhanced ACL Reconstruction on Return-to-sport Time, Function and Graft Outcomes in Patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093585
Enrollment
Unknown
Registered
2024-12-09
Start date
2025-01-15
Completion date
Unknown
Last updated
2024-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament injury

Interventions

Test Group:The subjects postoperative rehabilitation program will follow the "Accelerated Rehabilitation Program."
Control group:The subjects postoperative rehabilitation program will follow the "Standard Rehabilitation Program."
Case Series Study Group:The subjects postoperative rehabilitation program will follow the "Accelerated Rehabilitation Program."

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients with ACL injuries confirmed by imaging or arthroscopy, scheduled for ACL reconstruction. 2. Age: 18-45 years, with closed femoral and tibial growth plates. 3. Sports enthusiasts (participated in level 1 contact or non-contact sports (such as basketball, soccer, rugby, handball, cricket, etc. / tennis, badminton, skiing, etc.) at least once per week for a duration of at least 30 minutes per session within the year prior to injury, with a preoperative knee Tegner score of 5 or higher); professional athletes. 4. Willing to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe trauma leading to multiple ligament injuries (including posterior cruciate ligament injury, posterolateral corner injury, medial patellofemoral ligament injury, or grade II or higher medial collateral ligament injury). 2. Bilateral ACL injuries or functional impairment of the contralateral knee. 3. Concurrent tibial plateau fractures, severe cartilage damage, or existing osteoarthritis. 4. Previous surgeries on the knee joint (ipsilateral or contralateral). 5. Concurrent systemic diseases, such as malignant tumors, hematologic disorders, rheumatic diseases, and endocrine or metabolic diseases. 6. Minors under 18 years old, pregnant or breastfeeding women. 7. History of drug or alcohol abuse, cognitive impairment, or mental illness. 8. Inability to comply with postoperative treatment, rehabilitation, or follow-up requirements. 9. Any other condition that, in the investigator's opinion, makes the patient unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Time to Return to Unrestricted Sports;

Secondary

MeasureTime frame
P4 Pain Score;Knee injury and Osteoarthritis Outcome Score (KOOS);International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Form;Lysholm Score;Tegner Scale;ACL-Return to Sport after Injury (ACL-RSI) Score;KSS/CPA scale;heel to toe gait Test;Isokinetic Muscle Strength Test;Single Leg Hop Test;Landing Error Scoring System;Qualitative Assessment of Single-Leg Landing;T-Test;Modified Illinois Change of Direction Test;The Ballottement Test (for Patellar Tap Test);Range of Motion of the Knee Joint;Anterior Drawer Test; lachman test;Pivot Shift Test;Signal to Noise Quotient(SNQ);

Countries

China

Contacts

Public ContactZhao Jinzhong

Shanghai Sixth People's Hospital

jzzhao@sjtu.edu.cn+86 137 0757 1526

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026