Impingement Syndrome, Shoulder
Conditions
Brief summary
This study aims to investigate the relative effect of handgrip strengthening exercise in improving function, pain, strength, and active range of motion (AROM) of the shoulder among patients with primary sub-acromial impingement syndrome (SAIS).
Detailed description
The current study is a Single-Blind Randomized Clinical Trial to investigate the effectiveness of handgrip strengthening exercise in the treatment of patients with primary subacromial impingement syndrome. The randomization process will be based on concealed envelop picked up by participants.The patient will be conveniently recruited from the ministry of health hospitals in Jeddah.The patient who will meet the inclusion criteria; they will sign the consent form. The baseline data will be collected. The assessment will be carried out at the baseline, 4 weeks and 8 weeks; end of the treatment program; by the same blinded examiner for each patient and consist of the following instrument: Disabilities of Arm, Shoulder & Hand (DASH questionnaire), Visual analog scale (VAS), Hand-held dynamometer (HHD), and smartphone clinometer.
Interventions
BEHAVIORALHand grip strengthening
Handgrip strengthening exercises will be added to the experimental group. This exercise is chosen based on literature review of EMG and biomechanical studies. Adjustable heavy grip hand gripper will be used as handgrip resistance at 10 repetitions maximum (RM). The exercise will be performed in standing position the patient's back will be rested in a wall, arm at 30º abduction, 60º abduction 90º abduction & with 90º ER. In this positions, the patient will be performed 3 sets of 10 squeezes each at a 1-minute interval.
BEHAVIORALConventional treatment
Ultrasound therapy will be used to treat both groups. Ultrasound will be applied; while the patient will be seated in an adjustable chair with back support, feet on the floor. The chair will be positioned beside a table. The patient's shoulder will be rested on the table beside the body and elbow will be flexed at 90°. A round-headed probe will be used that is put in direct contact with the patient's skin over the shoulder joint. Ultrasound gel will be used on all surfaces of the head in order to reduce friction and assist in the transmission of the ultrasonic waves.
Sponsors
King Saud University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Willing to comply with all study procedures and be available for the duration of the study * Aged 18 to 45 * Diagnosed by their referring physician with subacromial impingement syndrome and has a positive impingement & rotator cuff test * Pain intensity between 3 to 8 in VAS
Exclusion criteria
* History of shoulder fracture or dislocation, osteophytes, and labral tear. * History of cardiac, neurological or musculoskeletal disease that precludes the ability to perform the exercise in the upper extremity. * Treatment with another intervention. * Hand or forearm dysfunction * Rheumatoid disease * Diabetic * History of shoulder, cervical, and thoracic surgery * Pregnancy * Malignancy * Symptoms for more than 1 year * Bilateral SAIS
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Function | Change from baseline functional score at 8 weeks | It will be assessed using the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire, which is a 30-item questionnaire that assess the ability of a patient to perform various upper extremity activities. it uses a 5-point Likert scale. A higher scores signify a greater level of disability, whereas, lower scores signify a lower level of disability. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Strength | Change from baseline muscle strength at 8 weeks | It will be assessed using HHD |
| Range of motion | Change from baseline range of motion at 8 weeks | It will be assessed using smartphone clinometer |
| Pain | Change from baseline pain intensity at 8 weeks | Pain intensity will be assessed using visual analog scale (VAS) (0 - 10 cm with 0 indicates no pain and 10 indicates the worst pain). |
Countries
Saudi Arabia
Contacts
Primary ContactSami Gabr, PhD
Outcome results
None listed