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

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190717044238N4

Enrollment

Registered

2023-03-01

Start date

2023-03-01

Completion date

Unknown

Last updated

2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adhesive Capsulitis of Shoulder. Adhesive capsulitis of shoulder

Interventions

Intervention 1: Intervention group 1: Gong's Mobilization. Procedure: Gong’s mobilization will be performed in a sitting/side-lying position.• The therapist will stand on the unaffected side of the su

Eligibility

Sex/Gender

All

Age

40 Years to 60 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Pakistan

Contacts

Public ContactHasha Asghar

Riphah International University, Lahore

drhashaasghar@gmail.com+92 317 0070706

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026