Adhesive Capsulitis Clinical Trial
Official title:
Effects of Combining Mobilization With Movement and Spencer's Technique in Diabetic Adhesive Capsulitis Patients
Verified date | September 2022 |
Source | Riphah International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will be a randomized control trial conducted on 44 patients diagnosed as adhesive capsulitis in headquarter hospital Gujar khan. Subjects will be divided equally into 4 groups (n=11 in each group) that are Group A, B, C and D by sealed envelope method. Pre-intervention assessment will be done by using data collection tools and then intervention will be applied. Group A will receive mobilization with movement (MWM) technique along with Spencer's muscle energy technique (MET) with conventional therapy. Group B will receive MWM along with conventional therapy. Group C will receive Spencer's MET along with conventional therapy. Group D will receive conventional therapy alone. All subjects will be given a home exercise plan. Assessment will be done after 1st session, 1st week, 2nd week, 3rd week and finally after 2 weeks on follow up using data collection tool. Data collection tools are semi-structured questionnaire (informed consent, demographic details, goniometric measurements), Visual analogue scale (VAS), shoulder pain and disability index (SPADI) and universal goniometer.
Status | Completed |
Enrollment | 44 |
Est. completion date | August 30, 2022 |
Est. primary completion date | July 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 70 Years |
Eligibility | Inclusion Criteria: - Both male and female - Age bracket is 30-70 years - Pain in the shoulder for at least three months - All active and passive shoulder movements restricted, with a reduction in external rotation of at least 50%. Exclusion Criteria: - Patients with - Recent history of surgery on particular shoulder - Post-traumatic and rotator cuff rupture - Neurological deficits affecting shoulder function - Pain or disorders of cervical spine, elbow, wrist or hand - Tendon calcification - Rheumatoid arthritis - Osteoporosis - Malignancies - Pregnancy - Open wounds or skin infections - Recent steroid injection - Previous manipulation under anesthesia of affected shoulder. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Tehsil headquarter hospital | Gujar Khan | Punjab |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Scale | A Visual Analogue Scale (VAS) is one of the pain rating scales used for measurement of pain intensity. The findings suggested that 100-mm VAS ratings of 0 to 4 mm can be considered no pain; 5 to 44 mm, mild pain; 45 to 74 mm, moderate pain; and 75 to 100 mm, severe pain. It will be used at baseline, after first session and then every week up to 6th week. | 6th week. | |
Primary | Shoulder Pain and Disability Index | The Shoulder Pain and Disability Index (SPADI) is a patient completed questionnaire with 13 items assessing pain level and extent of difficulty with Activity of daily Livings requiring the use of the upper extremities. The pain subscale has 5-items and the Disability subscale has 8-items.
It will be used at baseline, every week up to 4th week and then after 2 week follow up on 6th week |
6th week | |
Primary | Range of Motion | Ranges of motions of all shoulder movements will be measured. These include Flexion, Abduction, Eternal and Internal Rotation. It will be measured at baseline, after first session, every week up to 4th week and then after 2 week follow up on 6th week. | 6th week. |
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