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Gong Mobilization With and Without Thoracic Manipulation in Patients With Adhesive Capsulitis

Effects of Gong Mobilization With and Without Thoracic Manipulation on Pain, Range of Motion and Disability in Patients With Adhesive Capsulitis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07440680
Enrollment
36
Registered
2026-02-27
Start date
2025-01-02
Completion date
2025-09-28
Last updated
2026-02-27

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

Conditions

Adhesive Capsulitis

Keywords

Adhesive Capsulitis, Gong Mobilization, Thoracic Manipulation, Shoulder disability, Exercise Therapy

Brief summary

The study was conducted to determine effects of gong mobilization with and without thoracic manipulation on pain, range of motion and disability in patients with adhesive capsulitis.

Interventions

Gong mobilization was applied on affected shoulder joint in which distraction is applied followed by corrective AP force. Patient performs abduction and then prolong stretching of 7 seconds. It takes 2 to 3 minutes and is applied for three sessions per week for 4 weeks.

Thoracic manipulation was applied in prone position. Low amplitude high velocity thrust was applied at the end of available range at T4 and T5 after complete exhalation by the patient. intervention is applied for 3 times per week for 4 weeks.

OTHERConventional therapy

Conventional therapy includes heat therapy for 8 minutes, TENS for 20 mins. Stretches of posterior capsule, serratus anterior, pectoralis major and minor along with Codman exercises.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Age between 40 and 60 years * Both male and female * Clinically diagnosed with stage 2 frozen shoulder * Hypomobility of the thoracic spine * Unilateral or bilateral frozen shoulder with pain lasting for more than 3 month * Shoulder ROM limited with a flexion \<165°, abduction \<150°, or external rotation \<45°, restricted capsular pattern . * Positive shoulder shrug sign

Exclusion criteria

* Shoulder Arthritis * Thoracic outlet syndrome * Metabolic bone disease in the shoulder * Neoplastic bone disease in the shoulder * Osteoporosis and Osteomyelitis * Arm fracture, torn ligament around the shoulder joint, and shoulder surgery * Rheumatoid arthritis

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)From enrollment to the end of treatment at 4 weeksThe Numerical Pain Rating Scale (NPRS) is a unidimensional, patient-reported outcome measure used to assess the intensity of pain. Patients were asked for their pain intensity and then mark the number on the line according to their pain perception. The categorical variables of the NPRS are, none for 0, mild for value 1-5, moderate for 6-7 and severe for 8-10.
SPADI-Ufrom enrollment to the end of treatment at 4 weeksSPADI-U is a self-reported shoulder-specific outcome questionnaire by the evaluation of subjective clinical outcome measures. SPADI-U is an Urdu translated version of SPADI for cultural adaptation. It has a total of 13 items with 5 items related to pain and 8 items related to disability. The maximum score of SPADI-U is the same to that of SPADI i.e. 13. The scoring system includes the sum of all attempted questions divided by the maximum score and the multiply by 100 to find in percentage. Five items are designed to quantify pain, and eight items cover the disability measures of a patient with shoulder pathology.

Secondary

MeasureTime frameDescription
Shoulder flexion ROMFrom enrollment till end of treatment at 4 weeksChanges in shoulder flexion ROM at baseline and 4 weeks was measured using Goniometer
Shoulder Abduction ROMFrom enrollment till end of treatment at 4 weeksChanges in shoulder abduction ROM at baseline and 4 weeks was measured using Goniometer
Shoulder internal rotation ROMfrom enrollment till end of treatment at 4 weeksChanges in shoulder Internal rotation ROM at baseline and 4 weeks was measured using Goniometer
Shoulder external rotationFrom enrollment till end of treatment at 4 weeksChanges in shoulder external rotation ROM at baseline and 4 weeks was measured using Goniometer.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORHumera Mubashar, MS-OMPT

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026