Health Condition 1: M750- Adhesive capsulitis of shoulder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: People between the ages of 30 and 60 who have had shoulder pain for the past 3 to 6 months can take part in this study. Participants should be willing to join and should experience pain during both active and passive shoulder movements. They must also have a positive interscapular scratch test and report night-time pain with difficulty lying on the affected side.
Exclusion criteria
Exclusion criteria: Participants with open wounds, sub-acromial bursitis, rotator cuff tendinopathy or tears, fractures or dislocations of the shoulder joint, or gleno-humeral osteoarthritis will not be included in the study. Individuals who have received acupuncture treatment within the last one week will also be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS, SPADITimepoint: 3 WEEKS | — |
Secondary
| Measure | Time frame |
|---|---|
| A universal goniometer will be used to measure shoulder range of motion in participants with adhesive capsulitis by positioning the fulcrum at specific anatomical landmarks for each movement. Flexion will be measured by aligning the fulcrum with the lateral aspect of the greater tubercle, extension using the same axis, & abduction by placing the fulcrum at the anterior acromion. External rotation will be measured with the shoulder abducted to 90 degrees & the fulcrum positioned over the olecranon, while internal rotation will be assessed in the same position. Throughout the procedure, the scapula will be stabilised to prevent compensatory movements, & both active & passive ranges of motion will be recorded. All measurements will be repeated for accuracy. Participants in both groups will be assessed on Day 1 & Day 15Timepoint: 3 weeks | — |
Countries
India
Contacts
International Institute of Yoga and Naturopathy Medical Sciences