NCT06997692

Brief Summary

This study evaluates the effectiveness of Gong's mobilization combined with neuromuscular electrical stimulation versus conservative exercises in improving range of motion, pain relief, and functional outcomes in patients with adhesive capsulitis.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

February 1, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 21, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 30, 2025

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

May 30, 2025

Status Verified

May 1, 2025

Enrollment Period

4 months

First QC Date

May 21, 2025

Last Update Submit

May 21, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Visual Analog Scale (VAS

    Visual Analogue Scale (VAS) is one of the pain rating scales. Pain intensity can be categorized based on VAS scores, with mild pain typically ranging from 1-3, moderate pain from 4-6, and severe pain from 7-10.

    12 Months

  • Shoulder Pain and Disability Index (SPADI)

    The SPADI will be used to assess pain and disability. The pain subscale will measure the severity of pain during specific activities using a 0-10 numeric rating scale. The disability subscale will evaluate the difficulty experienced in performing daily activities involving the shoulder. SPADI scores will be recorded at the start of the treatment and again after completing the six treatment sessions to compare the changes in pain and functional status

    12 Months

Study Arms (2)

Gong's Mobilization with NMES

EXPERIMENTAL
Diagnostic Test: Gong's Mobilization with NMES

Comprehensive Conservative Physical Therapy

ACTIVE COMPARATOR
Combination Product: Comprehensive Conservative Physical Therapy

Interventions

Gong's Mobilization Technique: The participant will be positioned in a side-lying posture on a height-adjustable bed, with the affected side upward and the head supported by a pillow The therapist will apply an antero-posterior glide to the humeral head while stabilizing the scapula with the other hand. The participant will perform quick, powerful shoulder abduction in the coronal plane without external rotation or elbow flexion while the therapist maintains the mobilization force.

Gong's Mobilization with NMES

Thermal Modality Application: Participants will receive either a cold or hot pack (based on individual preference and clinical presentation) applied to the affected shoulder for 10-15 minutes. Cold packs will be wrapped in a thin towel and applied to

Comprehensive Conservative Physical Therapy

Eligibility Criteria

Age41 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Diagnosed cases of frozen shoulder confirmed by an orthopedician.
  • Patients in stage II or III of adhesive capsulitis.
  • Participants of both genders aged 41-60 years.
  • Subjects with a restricted range of motion (ROM), with losses of 25% or greater compared to the unaffected shoulder.

You may not qualify if:

  • Rotator cuff tears.
  • Overuse injuries.
  • History of rheumatoid arthritis, osteoarthritis, or malignancies in the shoulder region.
  • Adhesive capsulitis secondary to neurological disorders.
  • Unstable shoulders or recurrent dislocations.
  • Post-surgical cases involving the shoulder.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gosha shifa hospital lahore gulshan ravi A block

Lahore, Punjab Province, Pakistan

Location

MeSH Terms

Conditions

Bursitis

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 21, 2025

First Posted

May 30, 2025

Study Start

February 1, 2025

Primary Completion

June 1, 2025

Study Completion

January 1, 2026

Last Updated

May 30, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations