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Upper Thoracic and Postrior Shoulder sustained Stretch Glide

Effectiveness of Upper Thoracic Sustained Stretch Mobilization and Posterior Shoulder Strech Glide for Subacromial Impingement Syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220712055441N1
Enrollment
46
Registered
2022-07-15
Start date
2022-01-08
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

subacromial impingement syndrome. Impingement syndrome of shoulder

Interventions

Intervention 1: Group A will recieve upper thoracic (T1-T4) centrally postrio-anterior sustained stretch mobilization. The patient was in prone and a small pillow was placed under the chest. Therapis

Sponsors

Muhammad Institute of Medical and Allied Sciences, Multan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 45 Years

Inclusion criteria

Inclusion criteria: Both male and female, of age 25-45 years Patients with thoracic kyphosis >40o Patients with at least three positive physical tests from followings Neer impingement test, Hawkins kneddy test, Drop arm test, relocation test and apprehension test will be included. Patients often have painful arc between 70° and 120° pain on forced movement above the head

Exclusion criteria

Exclusion criteria: History of rotator cuff tear, shoulder and cervicothoracic surgery Patients of scapulothoracic dysfunction, sensory/ motor deficit and adhesive capsulitis Osteoporosis Surgery Fractures Dislocations Presence of thoracic scoliosis on Adam’s forward bend test

Design outcomes

Secondary

MeasureTime frame
Thoracic Kyphosis Angle. Timepoint: evaluated before and after treatment protocol. Method of measurement: sagittal plane radiograph in weight bearing position and arm folded 45o.

Primary

MeasureTime frame
Shouder Physical Disability. Timepoint: Evaluated before and after treatment. Method of measurement: Shoulder pain and disability index (SPADI).;Shoulder pain intensity,. Timepoint: evaluated before and after treatment. Method of measurement: Numeric pain rating scale (NPRS),.;Shoulder range of motion. Timepoint: evaluated before and after treatment. Method of measurement: Universal goniometer.

Countries

Pakistan

Contacts

Public ContactShahid Ishaq

Muhammad Institute of Medical and Allied Science

shahidishaq53@gmail.com+92 305 2032722

Outcome results

None listed

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