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FASCIAL DISTORTION MODEL vs. MANUAL THERAPY AND EXERCISES IN FROZEN SHOULDER

COMPARATIVE ANALYSIS OF FASCIAL DISTORTION MODEL, MOBILIZATION AND EXERCISES IN FROZEN SHOULDER: A RANDOMIZED CONTROLLED TRIAL - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087222
Enrollment
81
Registered
2025-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M750- Adhesive capsulitis of shoulder

Interventions

Intervention1: Fascial Distortion Model: Participants will receive FDM treatments, targeting specific fascial restrictions associated with a frozen shoulder depending upon the patient s verbal and non

Sponsors

JINDAL INSTITUTE OF MEDICAL SCIENCES, HISAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Subjects with frozen shoulder either unilateral or bilateral for at least 3 months. ii. Patients with three hallmark features of frozen shoulder i.e. insidious shoulder stiffness; severe pain, even at night; and near complete loss of passive and active external rotation of shoulder (Dias et al., 2005). iii. Both males and females between aged 40 to 60 years. iv. Subjects having gradual onset of shoulder pain, stiffness, difficulty in lying on affected side and pain in the shoulder sufficient enough to wake them at night. v. Subjects having problem in ADL s like dressing, combing hair and personal hygiene. vi. Those who provided their consent to participate in the trial.

Exclusion criteria

Exclusion criteria: i. Visible signs of oedema, hematomas, open wound or infections over the involved shoulder region ii. History of stroke or neurologically compromised patients. iii. Congenital deformities of the shoulder girdle like Klippel fiel, Sprengel s shoulder. iv. History (known case) of vascular diseases, aneurysms, arteriosclerosis, bleeding disorders, cancer, collagen vascular disease v. Phlebitis vi. Pregnancy

Design outcomes

Primary

MeasureTime frame
Shoulder Range of Motion, Shoulder Pain and Disability Index, Numeric Pain Rating Scale, Disability of Arm Shoulder and HandTimepoint: Baseline, Post Treatment, 1 Week, 2 Weeks, 4 Weeks

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactNaveen

Shri Guru Granth Sahib World University

drpankajpreetsingh@gmail.com9781533615

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026