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Clinical outcomes of isokinetic strength training in the enhanced recovery after surgery of total knee arthroplasty

Clinical outcomes of isokinetic strength training in the enhanced recovery after surgery of total knee arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076715
Enrollment
Unknown
Registered
2023-10-17
Start date
2023-10-17
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Knee Injuries

Interventions

Part I:6 weeks (2 times/week) of isokinetic strength training. Evaluate safety and rehabilitation effectiveness.
high-dose isokinetic strength training group (Part II):8 weeks (3 times/week) of high-dose isokinetic strength training
low-dose isokinetic strength training group (Part II):8 weeks (1 time/week) of low-dose isokinetic strength training
Health education group (Part II):Patients in the health education group did not receive strength training before admission. After baseline assessment, a joint health education was given to this group

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Part I: 1.Have done knee surgery before; 2.Age 18-75 years 3.Self-reported reduction in thigh muscle strength 4.BMI 3 months; 4. BMI < 35.

Exclusion criteria

Exclusion criteria: Part I: 1.Patients with diseases that cause pain or dysfunction of the lower limbs (lumbar disc herniation, Parkinson's, Alzheimer's, etc.); 2.Unable to walk short distances; 3.Severe cognitive impairment and communication disorders Part II: 1. History of arthroplasty in the lower limb; 2. History of injury and surgery in the past 6 months; 3. Receiving muscle strengthening or physical therapy in the past 6 months; 4. Other diseases that cause knee pain (such as rheumatoid arthritis, gout, etc.); 5. Other diseases that cause pain or dysfunction of the lower limbs (lumbar disc herniation, Parkinson's, Alzheimer's, etc.); 6. Unable to walk short distances independently (walking distance less than 100m); 7. Severe cognitive impairment and communication disorders; 8. Severe cognitive or communication impairments. 9. Knee valgus deformity >= 15°.

Design outcomes

Primary

MeasureTime frame
Isokinetic Muscle (Quadriceps and Hamstring) strength (Part l);Thigh (Quadriceps and Hamstrings) Cross-sectional Area (CSA) (Part I);KOOS score (Part II);Knee Joint Effusion (Part II);Inflammatory Factors (Part II);Knee Flexors and Extensors Muscle Strength (Part II);Joint Kinematics and Kinetics Parameters;

Secondary

MeasureTime frame
Self-assessment of Recovery (Part I);Walking Test (Part I);knee pain (Part I);Self-assessment of Knee Stability (Part I);intraoperative bleeding (Part II);Knee Joint Active Range of Motion (Part II);30s Sit-to-Stand Test (Part II);Timed-up-and-go test (Part II);Stair Climb Test (Part II);Surface Electromyography (EMG) Results (Part II);Balance Test Results (Part II);Self-Assessed Knee Joint Instability (Part II);Self-Assessed Fall Risk Questionnaire (Part II);Willingness to Undergo Surgery (Part II);Knee Joint Pain (Part II);Quadriceps and Hamstrings cross-sectional area (Part II);Lower Limb Strength Line (Part II);

Countries

China

Contacts

Public ContactNie Yong

West China Hospital, Sichuan University

nieyong1983@wchscu.cn+86 137 3064 1991

Outcome results

None listed

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