Shoulder Impingement Syndrome Clinical Trial
— SAISOfficial title:
The Effect of Mulligan Thoracic Sustained Natural Apophyseal Glides on Sub-acromial Impingement Syndrome.
Verified date | March 2023 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study was conducted to investigate the effect of mulligan thoracic sustained natural apophyseal glide on patients diagnosed as sub acromial impingement syndrome and its effect on shoulder range of motion, pain, function and disability of affected shoulder joint and size of sub acromial space, Half of the patients will treated with traditional treatment and mulligan thoracic SNAGS technique, while the other half will treated with traditional treatment only.
Status | Completed |
Enrollment | 74 |
Est. completion date | November 30, 2022 |
Est. primary completion date | November 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 40 Years |
Eligibility | Inclusion Criteria: 1. Patients referred as sub-acromial impingement syndrome (stage 2) according to neer's classification. 2. Have +ve Neer's sign, +ve Hawkins and Kennedy test and +ve Empty and full can tests. 3. selected from both genders. 4. Aged from 25 to 40 years old. 5. Have restricted thoracic extension motion ( +ve occiput to wall test). Exclusion Criteria: 1. History of shoulder adhesive capsulitis 2. Rotator cuff tendon tear/rupture (stage 3). 3. Shoulder dislocation, subluxation and fractures. 4. History of cervical, shoulder, upper back surgery. 5. Any spinal deformities such as scoliosis, kyphosis and rounded shoulder. 6. Diabetes mellitus. 7. Radiculopathy. 8. History of breast cancer. 9. Previous stroke or Shoulder hand syndrome. 10. Ligamentous Laxity. |
Country | Name | City | State |
---|---|---|---|
Egypt | faculty of physical therapy - Cairo university | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain by Visual analogue scale | the patient asked to choose from scale from zero (no pain) to 10 (worst pain) to detect his/her intensity of pain. | changes from baseline to before treatment and changes before treatment to immediately after treatment | |
Primary | Range of motion of shoulder joint by universal goniometer. | for flexion stationary Arm of the goniometer was aligned with the lateral border of the scapula (mid axillary arm), and the moving arm was aligned with the humerus.
for abduction the fulcrum was placed at the mid point of the posterior aspect of the glenohumeral joint, stationary arm was parallel to the trunk, and the moving arm was parallel to the longitudinal axis of the humerus. for internal and external rotation patient was in supine with the hips and knees flexed approximately 45°.The tested arm was supported on the table in 90° of abduction, elbow flexed 90°, and the wrist in neutral position. the fulcrum was placed on the olecranon, stationary arm Placed perpendicular to the floor, and the moving arm parallel with the forearm. |
changes from baseline to before treatment and changes before treatment to immediately after treatment | |
Primary | Shoulder pain and disability index | the patients will asked to answer the questions on index . And then creating a percentage of pain and disability with higher scores indicating more severe limitation. The means of the two subscales are averaged to produce a total score ranging from 0 (best) to 100 (worst).
Minimum Detectable Change (90% confidence) = 13 points |
changes from baseline to before treatment and changes before treatment to immediately after treatment | |
Primary | The sub-acromial space by radiograph X ray | measure the size of sub-acromial space | changes from baseline to before treatment and changes before treatment to immediately after treatment |
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