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Individualized rehabilitation of patients with anterior cruciate ligament reconstruction who returned to exercise after surgery

Individualized rehabilitation of patients with anterior cruciate ligament reconstruction who returned to exercise after surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087631
Enrollment
Unknown
Registered
2024-07-31
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-08-05

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

Control group:he patient received conventional knee rehabilitation methods after surgery, including ankle pump training, quadriceps isometric contraction, multi-direction straight leg elevation, heel
Research group:On the basis of routine training, patients in the research group added individualized training methods developed according to individual conditions. In order to reduce the risk of injur

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Age: =18 years old and < 40 years old; 2. A history of knee injury with limited active movement, strength and function of the knee for more than 6 months and no significant effect after 2 months of conservative treatment; 3. Physical condition permits knee arthroscopic surgery; 4. Anterior cruciate ligament injury was diagnosed by preoperative MRI results, requiring anterior cruciate ligament reconstruction surgery; 5. Voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous knee surgery; 2, there are significant comorbidities affecting limb control, such as Parkinson's disease; 3. Affected patients with knee joint injuries (including posterior cruciate ligament, collateral ligament, meniscus injury and patella dislocation); 4. Any deformity or lesion in the ankle or hip joint; 5. Unwilling/unable to complete the study follow-up or incomplete follow-up data;

Design outcomes

Primary

MeasureTime frame
Tegner ;

Secondary

MeasureTime frame
Visual Analogue Scale, VAS;Lysholm;ACL-RSI;Y balance test;Three-dimensional kinematic parameter;

Countries

China

Contacts

Public ContactChen Peng

The First Affiliated Hospital of Fujian Medical University

13506989645@163.com+86 135 0698 9645

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 8, 2026