patellar tendinopathy
Conditions
Interventions
Collaborative intervention group (experimental group):The PT collaborative intervention program combines sports, medicine, and education content, including exercise training methods, exercise intensit
Physical therapy group (control group):The physical therapy control group received extracorporeal shock wave therapy (ESWT), with patients in a supine position, knee flexion of 30 °, and a soft pillow
Health education group (control group):Adopting the health education approach in the collaborative inter
Sponsors
Shandong First Medical University Affiliated Neck, Shoulder, Waist, and Leg Pain Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. VISA P score<80 points (out of 100 points); 2.Meets PT diagnostic criteria; 3. At least six months of pain history; 4. The knee extension resistance test or single foot squat test is positive; 5. Heart, lung, brain, and mental illnesses; 6. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Acute knee or patellar tendon injury; 2. Late PT; 3. History of knee surgery; 4. Known hip and ankle inflammatory joint disease or familial hypercholesterolemia; 5. Use of drugs that have an effect on the patellar tendon (e.g., fluoroquinolones) within the past year; 6. Corticosteroid injections in or around the patellar tendon within the past month; 7. History of patellar tendon rupture; 8. Those who have used treatments that may affect the efficacy of this trial in the past two weeks (including exercise therapy); 9. Inability to walk or walk distance < 300m or unable to perform exercise training plan; 10. Physical examination or ultrasound/MRI showing other signs or symptoms of comorbid knee joint pathology and contraindications to MRI; 11. Have regular exercise habits; 12. Those with severe cardiovascular and cerebrovascular diseases, history of mental illness, cognitive impairment and contraindications to exercise therapy; 13. Those who are participating in other clinical trials and will affect the results of this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS pain score;Joint range of motion;Muscle Strength;Proprioceptive threshold;Foot tactile threshold;Berg Balance Score;Counter movement jump;VISA-P; | — |
Countries
China
Contacts
Public ContactLiu Wei
Shandong First Medical University Affiliated Neck, Shoulder, Waist, and Leg Pain Hospital
Outcome results
None listed