Menu
Recruiting NCT06686277

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

No phase Interventional Adhesive Capsulitis of Shoulder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Gong's Mobilization Technique, Mulligan Mobilization Technique.
Who it may be relevant to
Registry conditions: Adhesive Capsulitis of Shoulder. Basic parameters: 40 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects Of Gong's Versus Mulligan Mobilization On Pain, Range Of Motion, Functional Disability and Quality Of Life In Patients With Adhesive Capsulitis

Overview

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.

Interventions

  • Other Gong's Mobilization Technique
    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.
  • Other Mulligan Mobilization Technique
    Mulligan Mobilization Technique

Primary outcome measures

  • Level of Pain [Time frame: Pre & Post 6 weeks]
  • Range of Motion [Time frame: Pre & Post 6 weeks]
  • Functional Disability [Time frame: Pre & Post 6 weeks]
  • Quality of Life Level [Time frame: Pre & Post 6 weeks]

Eligibility criteria

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)

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)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Iffat Anwar Medical Complex — Lahore

Identifiers

NCT: NCT06686277 · REC/RCR&AHS/24/0116

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗