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An exploratory study on the recovery of meniscus repair function through exercise training assisted by wearable exoskeleton equipment

An exploratory study on the recovery of meniscus repair function through exercise training assisted by wearable exoskeleton equipment - An exploratory study of wearable exoskeleton equipment on functional recovery after meniscal repair surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098882
Enrollment
Unknown
Registered
2025-03-14
Start date
2024-03-10
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

meniscus injury

Interventions

Conventional rehabilitation group:Patients included in the conventional rehabilitation group will undergo postoperative rehabilitation treatment for 0-6 weeks that our department has currently impleme
Exoskeleton-assisted walking training group:All patients included in the exoskeleton-assisted walking training study underwent a 20-minute adaptive walking training assisted by a wearable exoskeleton

Sponsors

Fudan University Affiliated Huashan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged >=18 years old and less than 60 years old; 2) Patients who undergo unilateral knee arthroscopic surgery to repair meniscal injuries in our center and who have no restrictions on weight-bearing on the surgical side starting from the second day after surgery; 3) The difference in bilateral thigh circumference before surgery is less than 2 cm; 4) Skeletal muscle mass index (SMI) of limbs: male >=7.0kg/m2, female >=5.7kg/m2; 5) Grip strength of dominant hand: male >=26kg, female >=18kg; 6) The difference in bilateral thigh circumference after surgery is >3 cm; 7) You can be off crutches and fully weight-bearing three weeks after surgery; 8) The ankle joint on the affected side has sufficient passive movement angle. If there is plantar flexion contracture of the ankle joint, the contracture angle shall not exceed 5 degrees; 9) Able to understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients who have undergone surgery on the other knee joint; 2) Patients who are not undergoing surgery for the first time; 3) Combined treatment of patients with cartilage damage and ligament damage; 4) Patients with suspected tumors or nauseated tumors; 5) Systemic diseases causing knee joint symptoms such as gouty arthritis, rheumatoid arthritis, etc.; 6) Infection after knee joint surgery, poor wound healing, and joint range of motion not reaching 90° three weeks after surgery; 7) Prepatellar pain VAS pain score exceeds 2 points; 8) Combined with diabetes, hypertension, and thyroid dysfunction; 9) Patients who are unable to walk long distances due to other reasons; 10) Accompanied by severe musculoskeletal, cardiac, neurological, skin and vestibular system comorbidities; 11) Resting heart rate is lower than 50 beats/minute or higher than 100 beats/minute, resting blood pressure is lower than 90/60 mmHg or higher than 200/100 mmHg; 12) Any contraindications for exoskeleton use, such as: polyurethane allergy, pregnancy, leg length differences, height/weight restrictions, open ulcers at device contact points, etc.

Design outcomes

Primary

MeasureTime frame
Muscle thickness of medial head of quadriceps;Body Index;

Secondary

MeasureTime frame
Pain;knee function;quality of life;Lower limb dynamic monitoring;

Countries

China

Contacts

Public ContactYunshen Ge

Department of Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China

zhangshurong@huashan.org.cn+86 138 1768 0942

Outcome results

None listed

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