Electromyographic Activity of Posterior Oblique Sling Muscles in Patients With Shoulder Impingement Syndrome
EMG
1 other identifier
observational
60
1 country
1
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. .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedFirst Submitted
Initial submission to the registry
January 16, 2025
CompletedFirst Posted
Study publicly available on registry
January 23, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2025
CompletedJanuary 23, 2025
January 1, 2025
3 months
January 16, 2025
January 22, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
• electromyographic activity of posterior oblique sling muscles (gluteus maximus and latissimus dorsi)
EMG has been widely used for many decades, its use is proven and widely accepted by clinicians and the scientific community and it is considered the gold standard method for the measurement of muscle activity.
through study completion, an average of 4 months
Secondary Outcomes (3)
shoulder active range of motion
through study completion, an average of 4 months
shoulder function and disability level
through study completion, an average of 4 months
shoulder pain
through study completion, an average of 4 months
Study Arms (2)
Group A (control group)
controls
Group B (experimental group)
cases
Interventions
electromyographic activity of posterior oblique sling muscles will be measured
Eligibility Criteria
All patients will be referred by an orthopedic surgeon who will diagnose SIS based on clinical and radiological examination.
You may qualify if:
- Both male and female patients with shoulder impingement syndrome.
- patients complain from unilateral shoulder pain with chronic conditions of SIS ≥ 3 months.
- Patient age from 25 to 40 years.
- Patients with Positive impingement tests.
- Patients with painful arc of movement (60°- 120°)
You may not qualify if:
- Patients with Numbness or tingling of upper extremity.
- Patients with Shoulder fracture or previous shoulder surgery, and Acromioclavicular or shoulder dislocation.
- Patients with Any traumatic injury to the lower limb in the previous 6 months.
- Any spine surgery within the last 2 years.
- Patients with history of lower back pain in past 12 months .
- Patients with history of lower extremity dysfunctions in the past 12 months .
- Participants who had taken any drugs (e.g. statins and spasmed), which have effects on the skeletal muscles.
- Open wounds, rashes, psoriasis, skin irritations, or skin conditions of any kind in the region of electrode placement
- Participants with a Body Mass Index (BMI) ≥ 30
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Cairo University
Cairo, Giza Governorate, 12613, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Soheir S Rizk, PhD
Cairo University
- STUDY DIRECTOR
Aya A Khalil, PhD
Cairo University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator
Study Record Dates
First Submitted
January 16, 2025
First Posted
January 23, 2025
Study Start
January 1, 2025
Primary Completion
April 1, 2025
Study Completion
April 1, 2025
Last Updated
January 23, 2025
Record last verified: 2025-01
Data Sharing
- IPD Sharing
- Will not share