Electromyographic Activity of Posterior Oblique Sling Muscles in Patients With Shoulder Impingement Syndrome
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: electromyography.
- Who it may be relevant to
- Registry conditions: Shoulder Impingement Syndrome. Basic parameters: 25 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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
Interventions
- Device electromyography
electromyographic activity of posterior oblique sling muscles will be measured
Primary outcome measures
- • electromyographic activity of posterior oblique sling muscles (gluteus maximus and latissimus dorsi) [Time frame: through study completion, an average of 4 months]
Secondary outcome measures (3)
- shoulder active range of motion [Time frame: through study completion, an average of 4 months]
- shoulder function and disability level [Time frame: through study completion, an average of 4 months]
- shoulder pain [Time frame: through study completion, an average of 4 months]
Eligibility criteria
Inclusion criteria
- 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°)
Exclusion criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-control
Study locations
Egypt · 1 center
- Cairo University — Cairo
Identifiers
NCT: NCT06789991 · P.T.REC/012/005452 · P.T.REC/012/005452