Actively Recruiting

Phase Not Applicable
Age: 40Years - 65Years
All Genders
ID07328295

Additional Effects of Thoracic Spine Mobilization Combined With Glenohumeral Joint Mobilization on Pain, Range of Motion, and Functional Disability in Adhesive Capsulitis

Led by Foundation University Islamabad · Updated on 2026-01-09

34

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Adhesive capsulitis, also known as frozen shoulder, is a painful condition that limits shoulder movement and causes significant functional difficulties. Traditional treatments focus mainly on the shoulder joint itself, often overlooking the role of nearby areas like the thoracic spine. Recent findings suggest that improving thoracic spine mobility may help shoulder function, but this approach has not been widely tested for adhesive capsulitis. This study aims to assess whether adding thoracic spine mobilization to standard shoulder joint therapy can better relieve pain, improve range of motion, and enhance functional ability. The trial is a randomized controlled study where participants diagnosed with adhesive capsulitis will be assigned to one of two groups. One group will receive both thoracic spine mobilization and glenohumeral joint mobilization, while the other group will receive only glenohumeral joint mobilization. Thoracic spine mobilization involves specific oscillatory movements aimed at improving spinal extension and rotation, while shoulder mobilization includes targeted oscillations to restore joint movement. Treatments will be delivered over a set period, with techniques clearly defined for each group to compare their effects. Participants will be evaluated before and after treatment using the Numeric Pain Rating Scale to measure pain, the Shoulder Pain and Disability Index to assess functional limitations, and a goniometer to record shoulder range of motion. Data will be analyzed to determine if the combined treatment improves outcomes more than shoulder mobilization alone. The study will run for one year and aims to provide evidence supporting more comprehensive rehabilitation strategies for adhesive capsulitis.

CONDITIONS

Brief Title

Additional Effects of Thoracic Spine Mobilization Combined With Glenohumeral Joint Mobilization on Pain, Range of Motion, and Functional Disability in Adhesive Capsulitis

Who Can Participate

Age: 40Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female patients with unilateral or bilateral shoulder pain
  • Shoulder pain lasting at least 3 to 4 months
  • Decreased shoulder range of motion including external rotation, abduction, internal rotation, and flexion
  • Age between 40 and 65 years
  • Diagnosed with stage 2 or 3 adhesive capsulitis
Not Eligible

You will not qualify if you...

  • Shoulder pain caused by systemic diseases such as rheumatoid arthritis (morning stiffness over 1 hour, multiple small joint pain or swelling), infection, tumors, or myelopathy
  • Recent shoulder joint fracture or trauma
  • Thoracic outlet syndrome (positive Roos test)
  • Presence of cervical radiculopathy (positive Spurling's test)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive either thoracic spine mobilization combined with glenohumeral joint mobilization or glenohumeral joint mobilization only to improve shoulder pain, range of motion, and functional disability.

Multiple visits during the 4-week treatment period

Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Islamabad, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

L

Laiba Malik, DPT

M

Marwa Asim, MS-OMPT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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