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Effect of Gongs Mobilization With Neuromuscular Electrical Stimulation vs Conservative Exercises Among AC

Effect of Gongs Mobilization With Neuromuscular Electrical Stimulation vs Conservative Exercises Among Adhesive Capsulitis

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06997692
Enrollment
36
Registered
2025-05-30
Start date
2025-02-01
Completion date
2026-01-01
Last updated
2025-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adhesive Capsulitis

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.

Detailed description

Using a randomized controlled design with 36 participants with estimated drop out 10% will be 40, the study will measure changes in active and passive shoulder mobility and SPADI scores after 6 weeks.

Interventions

DIAGNOSTIC_TESTGong's Mobilization with NMES

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.

COMBINATION_PRODUCTComprehensive Conservative Physical Therapy

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

Sponsors

Superior University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
41 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS12 MonthsVisual 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.
Shoulder Pain and Disability Index (SPADI)12 MonthsThe 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

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026