Effects Of Gong's Versus Mulligan Mobilization In Patients With Adhesive Capsulitis
1 other identifier
interventional
60
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 24, 2024
CompletedFirst Submitted
Initial submission to the registry
November 12, 2024
CompletedFirst Posted
Study publicly available on registry
November 13, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 24, 2025
CompletedNovember 13, 2024
November 1, 2024
9 months
November 12, 2024
November 12, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Level of Pain
Numeric Pain Rating Scale
Pre & Post 6 weeks
Range of Motion
Goniometer
Pre & Post 6 weeks
Functional Disability
Shoulder Pain and Disability Index
Pre & Post 6 weeks
Quality of Life Level
Sort Form Survey-36
Pre & Post 6 weeks
Study Arms (2)
Gong's Technique Group
EXPERIMENTALThe subject will sat on knee-high chair with the spine in a neutral position and comfortably extends both their arms. Therapist will stand on the side opposite to the affected side. The therapist will push the scapula of the affected side in a posterior to anterior direction with one hand, and pushed the humeral head in an anterior to posterior direction parallel to joint plane with the other hand. Simultaneously, the subject will quickly and powerfully perform shoulder abduction with elbow flexion and with palm facing inside and the back of the hand facing outside. During this time, the hands of the therapist kept facing the humeral head with long axis of the palm along with the long axis of the humerus. The therapist followed the subject performing shoulder abduction, at the same speed while maintaining a little distraction, and adding acceleration in the end range.
Mulligan Mobilization
EXPERIMENTALFor shoulder abduction, therapist applied a posterolateral gliding force over the head of the humerus, while patient actively abducted his arm. For shoulder flexion, the therapist applied a posterolateral glide as patient flexed his shoulder. For shoulder internal rotation, therapist applied an inferior shoulder glide and stabilized the scapula as the patient internally rotated his shoulder, and adducted his upper arm. As the therapist pushed the shoulder into adduction in this way, the head of the humerus was distracted laterally. Therapist hand in the axilla acted as a fulcrum.For shoulder external rotation,therapist applied posterolateral glide in sitting position
Interventions
The therapist will push the scapula of the affected side in a posterior to anterior direction with one hand, and pushed the humeral head in an anterior to posterior direction parallel to joint plane with the other hand.
Eligibility Criteria
You may qualify if:
- Age 40 to 50 years
- Both male and female
- Pre-diagnosed Unilateral Primary Frozen shoulder patients
- Prediagnosed Stage 3(Frozen phase) patients(27)
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Iffat Anwar Medical Complex
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Hassan, MSPT
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Assessor blinded
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 12, 2024
First Posted
November 13, 2024
Study Start
April 24, 2024
Primary Completion
January 24, 2025
Study Completion
February 24, 2025
Last Updated
November 13, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share