Rotator cuff injury
Conditions
Interventions
Experimental group:Conventional Rehabilitation and Progressive Resistance Training with Blood Flow Restriction
Control group:Conventional rehabilitation and blood-flow restriction low-load resistance training
Sponsors
Hospital of Chengdu University of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Meets diagnostic criteria for rotator cuff injury but MRI shows no massive full-thickness rotator cuff tear; 2. Age 18–75 years; 3. Numeric Pain Rating Scale (NPRS) >= 3 within 24 hours; 4. Volunteers who participate in this study and sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with complete rotator cuff tears meeting surgical indications; 2. Severe loss of vital organ function (e.g., heart, liver, kidney); 3. Presence of contraindications related to blood flow restriction training: hypertension (systolic >140 mmHg, diastolic >90 mmHg), venous thrombosis, coagulation disorders, etc.; 4. Local skin damage or dermatological conditions; 5. Pregnant or lactating individuals, and patients with psychiatric disorders; 6. Individuals who have undergone prior shoulder surgery; 7. Patients with unstable vital signs, malignant tumors, or other severe medical conditions; 8. Individuals currently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric pain Rating Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Active and Passive Range of Motion of the Shoulder Joint;Shoulder Joint Muscle Strength Test;Shoulder Pain and Functional Impairment Index; | — |
Countries
China
Contacts
Public ContactTao Qin
Hospital of Chengdu University of Traditional Chinese Medicine
Outcome results
None listed