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Research on Robot Assisted Rehabilitation Training and Evaluation Methods

Research on Robot Assisted Rehabilitation Training and Evaluation Methods

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087381
Enrollment
Unknown
Registered
2024-07-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

Anterior cruciate ligament rupture, posterior cruciate ligament rupture, meniscus tear, patellar dislocation,SMA

Interventions

Experimental group:Performing isokinetic rehabilitation training under different stiffness conditions

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 8-60 years old. 2. Patients with unilateral anterior cruciate ligament (ACL) rupture (including partial meniscus tear). 3. Patients who have undergone unilateral anterior cruciate ligament reconstruction surgery for 3-6 months. 4. The cause of anterior cruciate ligament rupture is sports injury. 5. The subject or guardian is willing and able to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Simultaneously suffering from other major diseases or conditions. 2. Pregnant women, lactating women and other special populations. 3. Refusal to sign informed consent form or inability to complete the entire research process. 4. Currently infected with human immunodeficiency virus (HIV), infectious hepatitis B or C, or corresponding medical history. 5. Simultaneously suffering from medical problems, including but not limited to the following: (1) Uncontrolled hypertension (systolic blood pressure = 160mmHg and/or diastolic blood pressure = 95mmHg), congestive heart failure (New York Heart Association status classification III or IV). (2) Subjects with serum creatinine levels exceeding 2.0mg/dl (176.8 µ mol/L). (3) When screening, the total white blood cell (WBC) count is less than 2500/µ L, or platelets are less than 100000/µ L, neutrophils are less than 1500/µ L, or hemoglobin is less than 8.5 g/dL. (4) The patient is mentally incapable or unable to understand the requirements for participating in the study.

Design outcomes

Primary

MeasureTime frame
Knee peak torque;Knee average torque;Knee average work;

Secondary

MeasureTime frame
MMT muscle strength grade;Knee and thigh circumferences;Knee laxity;Muscle mass;Knee pain score;

Countries

China

Contacts

Public ContactYanggang Feng

Beihang University; Peking University Third Hospital

yanggangfeng@buaa.edu.cn+86 188 1172 8786

Outcome results

None listed

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