Rotator Cuff Syndrome, Rotator Cuff Tendonitis, Shoulder Pain Syndrome
Conditions
Brief summary
The current study will help to determine the efficacy of a rehabilitation protocol that involves the use of eccentric contraction for patients with shoulder pain syndrome. This approach aims to improve recovery in terms of pain and function based on scientific evidence.
Interventions
A 6-week rehabilitation program, conducted for two sessions per week. Patients will receive specialized eccentric contraction exercises for the shoulder muscles, administered in addition to a standard physical therapy protocol.
OTHERTraditional Physical Therapy Only
A 6-week standard rehabilitation program, conducted for two sessions per week. Patients will receive Traditional physical therapy interventions only, which include ultrasound, range of motion (ROM) exercises, postural training and general strengthening routinely prescribed."
Sponsors
Rafeef Hassan Asiri
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
14 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* 18-70 years old patient, female and male diagnosed with Shoulder pain syndrome and reliable patients who can follow orders. * Patient diagnosed by rotator cuff tendinitis
Exclusion criteria
* Patient with VAS more than 8/10 * History of shoulder, cervical, or thoracic surgery, shoulder dislocation, fracture, and labral tear, full thickness rotator cuff tear and adhesive capsulitis, rheumatic disease and / or any medical condition that prevents patient to perform resisted exercises * Neoplastic disease, and systemic inflammatory disease * Participants with three positive rotator cuff tear tests were likely to have a full-thickness rotator cuff tear and were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from Baseline in Pain Intensity using the Visual Analog Scale (VAS) | Baseline and at the end of the 6-week intervention period. |
| Change from Baseline in Shoulder Pain and Disability using the Shoulder Pain and Disability Index (SPADI) | Baseline and at the end of the 6-week intervention period. |
Secondary
| Measure | Time frame |
|---|---|
| Change from Baseline in Functional Independence using the Functional Independence Measure (FIM) | Baseline and at the end of the 6-week intervention period. |
Countries
Saudi Arabia
Outcome results
None listed