Comparative Effects of Gong’s Mobilization and Mobilization with Movement on Pain, Range of Motion and Functional Disability in Patients with Adhesive Capsulitis

Phase 3

Conditions: Adhesive Capsulitis of Shoulder.
Adhesive capsulitis of shoulder
M75.0

Registration Number: IRCT20190717044238N4

Lead Sponsor: Riphah International University Lahore

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 60

Inclusion Criteria

Male & female patients
Age group 40 to 60 years
Subjects clinically diagnosed with grade 2 adhesive capsulitis
Painful and limited active and passive glenohumeral ROM >25% in capsular pattern (limited external rotation then abduction and then flexion
Pain in the shoulder for at least 3 months

Exclusion Criteria

History of surgery on effected shoulder.
History of fracture around shoulder complex.
History of pain or disorders of the cervical spine, elbow, wrist, or hand.
History of any other pathological conditions involving the shoulder (rotator cuff tear, tendinitis, etc.) Hawkins-Kennedy test, empty can test will be used to exclude other shoulder conditions.
History of neurological deficits limiting shoulder during activities of daily living

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Total intervention protocol will be given for four weeks of duration, 3 sessions per week with total 12 sessions. Outcomes will be assessed at baseline, at the end of 2 week (6th session) and at the end of 4th week (12th session). Method of measurement: Numeric Pain Rating Scale (NPRS).;Range of Motion (ROM). Timepoint: Total intervention protocol will be given for four weeks of duration, 3 sessions per week with total 12 sessions. Outcomes will be assessed at baseline, at the end of 2 week (6th session) and at the end of 4th week (12th session). Method of measurement: Universal Goniometer.;Disability. Timepoint: Total intervention protocol will be given for four weeks of duration, 3 sessions per week with total 12 sessions. Outcomes will be assessed at baseline, at the end of 2 week (6th session) and at the end of 4th week (12th session). Method of measurement: SPADI- Shoulder pain and disability index.

Secondary Outcome Measures