Effects Of Gong's Versus Mulligan Mobilization In Patients With Adhesive Capsulitis

Not Applicable

Recruiting

• Conditions: Adhesive Capsulitis of Shoulder

• Registration Number: NCT06686277
• Lead Sponsor: Riphah International University

Brief Summary

A Randomized Clinical Trial will be conducted at DHQ hospital kasur,BIT hospital kasur,Arif memorial hospital Lahore.Pre-diagnosed patients will be reassessed by applying (Shoulder Shrug Sign, Hand to neck, Hand to scapula, Hand to opposite scapula,Hand to back,Capsular pattern movement restriction)Plus all other special tests will be applied to confirm that symptoms are not due to other shoulder pathologies but are due to just adhesive capsulitis then through consecutive sampling technique on 60 patients they will be allocated using computer generated sampling(random number table) into Group A and Group B.

Detailed Description

A Randomized Clinical Trial will be conducted at DHQ hospital kasur,BIT hospital kasur,Arif memorial hospital Lahore.Pre-diagnosed patients will be reassessed by applying (Shoulder Shrug Sign, Hand to neck, Hand to scapula, Hand to opposite scapula,Hand to back,Capsular pattern movement restriction)Plus all other special tests will be applied to confirm that symptoms are not due to other shoulder pathologies but are due to just adhesive capsulitis then through consecutive sampling technique on 60 patients they will be allocated using computer generated sampling(random number table) into Group A and Group B. Group A will be treated with Gong's mobilization and Group B will be treated with Mulligan MWM The procedures will be performed Three sets of 10 repetitions, with 1 minute rest between sets,thrice per week for a total of six weeks. Pre and post intervention values will be taken on 1st day and after 6 weeks. Outcome measures will be conducted through VAS for pain,SPADI for functional disability , goniometer for range of motion ,SF-36 for quality of life after 6 weeks. Data will be analyzed during SPSS software version 25. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2024-04-24
• Status Verified: 2024-11
• Study First Submitted: 2024-11-12
• Study First Submitted QC: 2024-11-12
• Last Update Submitted: 2024-11-12
• Study First Posted: 2024-11-13
• Last Update Posted: 2024-11-13
• Primary Completion: 2025-01-24
• Study Completion: 2025-02-24

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Age 40 to 50 years
• Both male and female
• Pre-diagnosed Unilateral Primary Frozen shoulder patients
• Prediagnosed Stage 3(Frozen phase) patients(27)

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Exclusion Criteria

• Patients with previous surgery in the shoulder joint
• History of recent fracture or severe trauma to the shoulder
• Diagnosed instability or previous history of dislocation
• Systemic inflammatory conditions(e.g.rheumatoid arthritis)

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Functional Disability	Pre & Post 6 weeks	Shoulder Pain and Disability Index
Quality of Life Level	Pre & Post 6 weeks	Sort Form Survey-36
Level of Pain	Pre & Post 6 weeks	Numeric Pain Rating Scale
Range of Motion	Pre & Post 6 weeks	Goniometer

Trial Locations

Locations (1)

Iffat Anwar Medical Complex; 🇵🇰 Lahore, Punjab, Pakistan