NCT07322198

Brief Summary

This study aims to compare the effectiveness of Gongs Mobilization with and without scapular High-lift in the management of Adhesive Capsulitis, focusing on specific outcomes like pain, functional outcomes, and work productivity.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

3 active sites

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress56%
Mar 2026Jun 2026

First Submitted

Initial submission to the registry

December 22, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

January 7, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

March 1, 2026

Completed
29 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Expected
Last Updated

January 7, 2026

Status Verified

December 1, 2025

Enrollment Period

29 days

First QC Date

December 22, 2025

Last Update Submit

December 22, 2025

Conditions

Keywords

adhesive capsulitisshouldercapsulitisgongs mobilizationscapular high-lift

Outcome Measures

Primary Outcomes (1)

  • NUMERICAL PAIN RATING SCALE (NPRS)

    It is a fundamental tool used to evaluate pain intensity and pain tolerance. Subjects can rate their pain from 0 (no pain at all) to 10 (pain as bad as it could be) to check whether the pain is acute or chronic. 42. The test-retest reliability coefficient, the intra-class correlation coefficient (ICC) for NPRS, is 0.74, and the minimal clinically important difference (MCID) is 1.1 points

    4 Weeks

Secondary Outcomes (2)

  • SHOULDER PAIN AND DISABILITY INDEX (SPADI)

    4 Weeks

  • UNIVERSAL GONIOMETERY:

    4 Weeks

Study Arms (2)

GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS)

EXPERIMENTAL

GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS) containing 21 participants who will be given Gong's mobilization with scapular high lifts for 30 minutes along with the conventional physiotherapy.

Other: Experimental: GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS)

GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS)

EXPERIMENTAL

GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS) containing 21 participants who were given Gong's mobilization without scapular high lifts for 30 minutes along with the conventional physiotherapy

Other: Experimental: GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS)

Interventions

Patients received Gong's mobilization without allowing scapular high lifting. The therapist applied a lateral glide to the humeral head while the patient performed pain-free shoulder elevation or abduction. Scapular movement was controlled to avoid compensation, aiming to reduce pain and improve shoulder mobility and function.

GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS)

In this technique, the therapist applies a sustained lateral glide to the humeral head while the patient actively performs shoulder elevation or abduction. Scapular high lifting is encouraged during the movement to assist shoulder elevation. The technique is performed within a pain-free range to reduce pain and improve shoulder mobility and functional movement.

GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS)

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Participants, including both males and females.
  • aged 40 to 60 years.
  • Diagnosed with unilateral Adhesive capsulitis at the 2nd or 3rd stage of the disease

You may not qualify if:

  • History of any trauma, tumor, fracture, surgery, or infection in a shoulder joint.
  • Patient with pregnancy and a history of abnormal neurological status (radiculopathy, stroke with hemiplegia, brachial plexus injury).
  • Restricted shoulder due to burns or postoperative scars.
  • Moderate or High levels of diabetes.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Bethania Hospital Sialkot

Sialkot, Punjab Province, 51040, Pakistan

Location

Raheem Surgical Hospital Sambrial

Sialkot, Punjab Province, 51310, Pakistan

Location

University of Management and technology Sialkot Campus

Sialkot, Punjab Province, 51310, Pakistan

Location

Related Publications (3)

  • Challey T, Dutta2 A, Kalita A, Pyngrope4 HR. Effectiveness of Gong's Mobilization Over Myofascial Release Technique in Patients with Adhesive Capsulitis.: Life Sciences-Physiotherapy. International Journal of Life Science and Pharma Research. 2023 May 1;L134-44.

    RESULT
  • Eldridge A, Lohman E, Asavasopon S, Gharibvand L, Michener L. External handheld loads affect scapular elevation and upward rotation during shoulder elevation tasks. Int Biomech. 2024 Dec;11(1):1-8. doi: 10.1080/23335432.2024.2332212. Epub 2024 Mar 19.

  • Poulose R, Navya T.V, Pawani DJ. A STUDY ON EFFECTIVENESS OF SCAPULAR PNF TECHNIQUES ON PAIN AND DYNAMIC STABILITY OF SCAPULA IN ADHESIVE CAPSULITIS OF SHOULDER JOINT. IJMAES. 2025;11(01):2271-86.

    RESULT

MeSH Terms

Conditions

Bursitis

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Study Officials

  • HAMZA ZAHID, MS OMPT

    University of Management and Technology Sialkot Pakistan

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head Of Department (HOD)

Study Record Dates

First Submitted

December 22, 2025

First Posted

January 7, 2026

Study Start

March 1, 2026

Primary Completion

March 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

January 7, 2026

Record last verified: 2025-12

Locations