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Evaluation of Long-term Isokinetic Training of Knee Joint

Effect and Evaluation of Long-term Isokinetic Training of Knee Joint Under the Influence of Stiffness

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06674473
Enrollment
12
Registered
2024-11-05
Start date
2024-11-06
Completion date
2026-10-20
Last updated
2026-09-15

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

Conditions

Knee Injuries and Disorders

Brief summary

The goal of this clinical trial is to assess the effectiveness of isokinetic rehabilitation training under optimal stiffness in patients undergoing knee joint rehabilitation. The main questions it aims to answer are: * Does isokinetic training under optimal stiffness lead to greater force exertion compared to traditional bodyweight training? * What are the long-term (6-week) effects of isokinetic training under optimal stiffness on joint flexibility and muscle strength? Researchers will compare the effects of isokinetic training under optimal stiffness to traditional bodyweight training to see if isokinetic training produces superior improvements in muscle strength, flexibility, and overall functional recovery. Participants will: * Perform regular training sessions using a portable knee joint isokinetic trainer, customized to their optimal stiffness for maximum force exertion. * Engage in a 6-week rehabilitation program, with assessments at the beginning, and end of the study to evaluate changes in muscle strength, and functional recovery.

Interventions

DEVICEWith robot assistance

Use a portable isokinetic device

BEHAVIORALtraditional rehabilitation

Use traditional isotonic and isometric rehabilitation

Sponsors

Peking University Third Hospital
Lead SponsorOTHER
Beihang University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Age between 20-60 years. 2. Patients with unilateral anterior cruciate ligament (ACL) rupture (with or without meniscus injury), posterior cruciate ligament (PCL) rupture, meniscal tear (M), and patellar dislocation (PD). 4\. Postoperative period of 3-6 months. 5. No restriction in knee extension or flexion movements.

Exclusion criteria

1. Patients with major diseases or conditions such as coronary heart disease, myocardial infarction, heart failure, cerebral infarction, cerebral hemorrhage, or malignant tumors. 2. Pregnant or breastfeeding women and other special populations. 3. Patients who refuse to sign the informed consent form or are unable to complete the entire study process. 4. Patients currently infected with human immunodeficiency virus (HIV), or with a history of infectious hepatitis B or C. 5. Patients with concurrent medical issues, including but not limited to: (1) Uncontrolled hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥95 mmHg), congestive heart failure (New York Heart Association functional classification of stage III or IV). (2) Patients with mental incapacity or an inability to comprehend the study requirements.

Design outcomes

Primary

MeasureTime frameDescription
Cross-sectional area of the quadricepsBefore 1st practice, and after 12th practice (6 weeks * 2 practices/week = 12 practices)Using MRI,Up to 6 weeks
Cross-sectional area of the hamstringsBefore 1st practice, and after 12th practice (6 weeks * 2 practices/week = 12 practices)using MRI, Up to 6 weeks
Peak flexion and extension knee torqueDuring each practice (6 weeks * 2 practices/week = 12 practices).Using an integrated torque sensor
Average flexion and extension knee torqueDuring each practice (6 weeks * 2 practices/week = 12 practices).
Flexion and extension knee workIn each ptractice (6 weeks * 2 practices /week = 12 practices).Work=Torque\*Speed

Secondary

MeasureTime frameDescription
Thigh circumferenceIn each ptractice (6 weeks * 2 practices /week = 12 practices).10 cm proximal to the superior pole of the patella
Knee joint pain score (VAS score)Before 1st practice, and after 12th practice (6 weeks * 2 practices/week = 12 practices)Up to 6 weeks,max. =100, min. =0, Visual Analogue Scale=VSA, A higher score indicates greater pain intensity.
Surface electromyography signals of quadricep and hamstringsDuring optimal stiffness measurementsSEMG signals are used to evaluate the instant effect brought by the optimal stiffness.

Countries

China

Contacts

CONTACTYuanzhen Yuan, Dr.
yanggangfeng@buaa.edu.cn+8618811728786

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026