Scapular Mobilization and Proprioceptive Neuromuscular Facilitation on Shoulder Dysfunction After… (NCT07547982) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Scapular Mobilization and Proprioceptive Neuromuscular Facilitation on Shoulder Dysfunction After Latissimus Dorsi Flap Breast Reconstruction
36 participantsStarted 2026-04-25
Plain-language summary
this study will be conducted to investigate the effect of scapular mobilization and scapular Proprioceptive neuromuscular facilitation on shoulder dysfunction after latissimus dorsi flap breast reconstruction
Who can participate
Age range40 Years – 55 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* age ranged from 40 to 55 years.
* All patients were female patients suffering from shoulder dysfunction after latissimus dorsi flap breast reconstruction.
* All patients suffering from moderate or severe pain on shoulder joint and limited range of motion that may affect daily activities.
* All patients begun the treatment program 3 to 4 weeks after LDF breast reconstruction.
* Informed consent was obtained from every patient enrolled in the trial.
Exclusion Criteria:
* Current metastases.
* Neurological deficit affecting the shoulder functioning during daily activities.
* Pathology of the shoulder joint including rotator cuff tear adhesive capsulitis and tendinitis.
* Pain or disorder of the cervical spine, elbow, wrist or hand.
* Shoulder surgery, shoulder dislocation fracture acromioclavicular joint osteoarthritis.
* Diabetes.
* Pregnancy.
* Shoulder manipulation under anesthesia, local corticosteroid injection.
* Psychological disorders.