Electromyographic Activity of Posterior Oblique Sling Muscles in Patients With Shoulder Impingement Syndrome

NCT ID: NCT06789991

Last Updated: 2025-01-23

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 60 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-01-31
• Study Completion Date: 2025-04-30

Brief Summary

this study aims to assess the gluteus maximus muscle electromyographic activity and the latissimus dorsi muscle electromyographic activity in patients with shoulder impingement syndrome , to improve the assessment procedure and the rehabilitation program for treating patients with shoulder impingement syndrome more effectively. .

Detailed Description

background: Shoulder pain is the third most common musculoskeletal complaint that can lead to disability that interfere with work, hobbies, social, and sporting activities and may also be associated with psychological distress and reduced quality of life .Shoulder impingement syndrome Symptoms is the most common cause of shoulder pain.

Normal shoulder movement is achieved through a stable lumbopelvic-hip complex and scapula. Thus, the pelvis must provide a stable platform for the scapula and the scapula provide a stable platform for the shoulder. The existing evidence supports myofascial biomechanical connection between lumbopelvic region and contralateral glenohumeral joint .So Considering the LP region and related myofascial force transmission as contributing factors for shoulder pathogenesis can explain the reasoning on why some of the patients with shoulder pain may progress to develop chronic shoulder pain.

purpose: this study aims to assess the gluteus maximus muscle electromyographic activity and the latissimus dorsi muscle electromyographic activity in patients with shoulder impingement syndrome , to improve the assessment procedure and the rehabilitation program for treating patients with shoulder impingement syndrome more effectively.

methods: This study is a cross sectional comparative study will be conducted at the out-patient physical therapy clinic, Pharos University in Alexandria, Egypt. 30 patients with unilateral shoulder impingement and 30 healthy controls without shoulder impingement , with age range between 25 and 40 years will be included in the study. All patients will be referred by an orthopedic surgeon.

results: data analysis with one-way ANOVA will be used to compare between subjects characteristics of the two groups and un-paired t-test will be used to compare measured variables between groups.

keywords: shoulder impingement syndrome, posterior oblique sling , electromyography , latissimus dorsi , gluteus maximus

Conditions

Shoulder Impingement Syndrome

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Group A (control group)

controls

electromyography

Intervention Type: DEVICE

electromyographic activity of posterior oblique sling muscles will be measured

Group B (experimental group)

cases

electromyography

Intervention Type: DEVICE

electromyographic activity of posterior oblique sling muscles will be measured

Interventions

electromyography

electromyographic activity of posterior oblique sling muscles will be measured

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Both male and female patients with shoulder impingement syndrome.

2. patients complain from unilateral shoulder pain with chronic conditions of SIS ≥ 3 months.

3. Patient age from 25 to 40 years.

4. Patients with Positive impingement tests.

5. Patients with painful arc of movement (60°- 120°)

Exclusion Criteria

1. Patients with Numbness or tingling of upper extremity.

2. Patients with Shoulder fracture or previous shoulder surgery, and Acromioclavicular or shoulder dislocation.

3. Patients with Any traumatic injury to the lower limb in the previous 6 months.

4. Any spine surgery within the last 2 years.

5. Patients with history of lower back pain in past 12 months .

6. Patients with history of lower extremity dysfunctions in the past 12 months .

7. Participants who had taken any drugs (e.g. statins and spasmed), which have effects on the skeletal muscles.

8. Open wounds, rashes, psoriasis, skin irritations, or skin conditions of any kind in the region of electrode placement

9. Participants with a Body Mass Index (BMI) ≥ 30

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cairo University

OTHER

Sponsor Role: lead

Responsible Party

nada mohamed ahmed emara

principle investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Soheir S Rizk, PhD

Role: STUDY_CHAIR

Cairo University

Aya A Khalil, PhD

Role: STUDY_DIRECTOR

Cairo University

Locations

Cairo University

Cairo, Giza Governorate, Egypt

Countries

Egypt

Central Contacts

nada M emara, BSc

Role: CONTACT

nada.emara@pua.edu.eg

00201005281592

Facility Contacts

Sohier S Rizk, PhD

Role: primary

sohair.shehata@pt.cu.edu.eg

0020124003374

Aya A Khalil, PhD

Role: backup

aya.abdelhamid@pt.cu.edu.eg

00201112204944

Other Identifiers

P.T.REC/012/005452

Identifier Type: OTHER

Identifier Source: secondary_id

P.T.REC/012/005452

Identifier Type: -

Identifier Source: org_study_id