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The Effects of Neuromobilization in Patients With Shoulder Impingement Syndrome on Pain,Strength,Range of Motion and Functional disability Score

The Effects of Neuromobilization in Patients With Shoulder Impingement Syndrome on Pain,Strength,Range of Motion and Functional disability Score.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190121042445N1
Enrollment
80
Registered
2019-02-19
Start date
2637-11-06
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

patients suffering from shoulder impingement syndrome lead impairment of daily activities and reduction in work capacity. Most of patients have painful symptoms at night and during abduction which may affect the sleep and daily activities.Forty percent of the populations possibly suffer from shoulder pain at some point of their life time..

Interventions

Intervention 1: Intervention group: Neuromobilization was applied using Butler’s recommendations.Procedure
Initially, the patient performed neural sliders and gradually progressed to neural tensioners. Neural sliders consisted of cervical lateral flexion movement, toward the involved side, simultaneously w

Sponsors

Social Security Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Positive Impingement Sign Age Between 20-50 years Patient with Positive Special Tests (Neers Test, Hawkins Kennedy Test, Empty Can Test)

Exclusion criteria

Exclusion criteria: Patients with co-morbidity such as Cervical Radiculopathy, Acromioclavicular Joint Pathology and Shoulder Dislocation/ Subluxation/ Fracture. Patients with history of Cervical, Shoulder of Upper Back Surgery

Design outcomes

Primary

MeasureTime frame
Pain Intensity. Timepoint: before intervention, 5th week and 11th week after intervention. Method of measurement: Pain by Visual Analogue Scale.;Range of motion. Timepoint: Before intervention, on 5th week and on 11th week. Method of measurement: Measured by Goniometry.

Secondary

MeasureTime frame
Shoulder Strength. Timepoint: Before intervention, on 5th week and on 11th week. Method of measurement: Strength by Hand held dynamometer.;Functional disability score. Timepoint: Before intervention, on 5th week and on 11th week. Method of measurement: UCLA Score.

Countries

Pakistan

Contacts

Public ContactHossein Karimi

The University of Lahore

hkarimi.pt.uos08@gmail.com

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 17, 2026