Cervical Unilateral Antero-posterior Mobilization and Thoracic Central Postro-anterior Mobilization in Treatment of Shoulder Impingement Syndrome

Shoulder Impingement Clinical Trial

Official title:

The Addition of Cervical Unilateral Antero-posterior Mobilization and Thoracic Central Postro-anterior Mobilization to Selected Therapeutic Exercise Program in Treatment of Shoulder Impingement Syndrome: A Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06349746
• Other study ID #: collage of physical therapy
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 15, 2024
• Est. completion date: June 2024

Study information

• Verified date: April 2024
• Source: Egyptian Chinese University
• Contact: Noha Elserty
• Phone: 01006709648
• Email: noha_elserty[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Shoulder impingement syndrome (SIS) is a complex, multi-factorial problem that is treated with a variety of different conservative options. The conservative option that has shown effectiveness is manual therapy of the cervical and thoracic spine

Description:

This study will be conducted to answer the following question:

What is the effect of adding cervical and thoracic mobilization to selected therapeutic exercise Program on pain intensity, Pain-free shoulder flexion and scaption active ROM, muscle strength of external rotator and abductors, shoulder functional status in patients with Shoulder Impingement Syndrome

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 50
• Est. completion date: June 2024
• Est. primary completion date: May 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 45 Years

Eligibility

Inclusion Criteria:

• • patients who had received at least two positive signs on their Neer sign, Hawkins sign, supraspinatus test, apprehension test, and relocation test

• Patients report pain on elevating the arm between 70 ° and 120 ° (the "painful arc"), on forced movement above the head, and when lying on the affected side

Exclusion Criteria:

• • cervical radiculopathy

• a history of shoulder surgery

• corticosteroid injection within the past month

• Subjects who had received physical therapy treatment for their shoulder within the past three months.

Related Conditions & MeSH terms

• Shoulder Impingement
• Shoulder Impingement Syndrome

Intervention

Other:
• therapeutic exercises
stretching exercise to posterior capsule and progressive resistance exercise for rotator cuff and scapula stabilizer and home exercise 3 sessions per week for 6 week.
• mobilization exercise
cervical unilateral antero-posterior mobilization and thoracic central postro-anterior mobilization

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Egyptian Chinese University	Benha University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pain intensity	pain intensity will be measured by visual analogue scale	pre intervention and after 6 weeks of intervention
Primary	shoulder flexion and abduction range of motion	measurement of shoulder flexion and abduction range of motion applied by using digital goniometer	pre intervention and after 6 weeks of intervention
Primary	muscle strength	shoulder flexors and external rotators muscle strength will be measured by dynamometer	pre intervention and after 6 weeks of intervention