Effectiveness of Neuromuscular Electrical Stimulation in Patients With Subacromial Impingement Syndrome: Randomized Controlled Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Subacromial Impingement Syndrome
- Sponsor
- Istanbul University - Cerrahpasa (IUC)
- Enrollment
- 48
- Locations
- 1
- Primary Endpoint
- Disability Arm Shoulder Hand Questionnaire (DASH)
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
Subacromial Impingement Syndrome (SIS) is one of the musculoskeletal system problems. SIS, which is the most common cause of shoulder pain, constitutes 44-65% of complaints of shoulder pain. Studies have shown that exercise is effective in treating patients with SIS, but the effectiveness and superiority of Neuromuscular Electrical Stimulation (NMES) to each other is uncertain. NMES is widely applied in physiotherapy. In the SIS, the lower trapezius and serratus anterior muscle are affected. Therefore, our aim is to determine the effects of exercises and NMES used in patients with SIS on pain, range of motion (ROM), muscle strength and functional status, neck pain and sleep quality.
Detailed Description
The aim of this study investigate exercise training (ET) and ET combined with Neuromuscular Electrical Stimulation (NMES) on pain, range of motion (ROM), functional capacity, neck pain, sleep quality. The study will be included 48 volunteers with Subacromial Impingement Syndrome (SIS). The study's inclusion criteria are as follows: Having a diagnosis of subacute / chronic extrinsic SIS, 18 to 65 years of age and being volunteer. The exclusion criteria are as follows: Fracture or surgical history in the shoulder region, another diagnosis that can affect shoulder function, having received local corticosteroid injection / treatment in the shoulder joint within the last 3 months, neuromuscular disease, pregnancy, cancer, unstabil angina, communication problems, systemic inflammatory joint disease, situations where electrical stimulation and exercise are contraindicated, orthopedic, rheumatologic or congenital disease of the affected upper extremity. The sociodemographic data of the patients will be questioned. ET will be applied daily and NMES will be applied 2 days a week for 8 weeks. In addition, both groups will apply these exercises as a home program 3 times a day, 10 repetitions of each exercise. Pain intensity with Visual Analog Scale (VAS), range of motion (ROM) with goniometer, muscle strength with Hand-held Dynamometer, upper extremity function evaluation with Quick Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire, disability of neck level with Neck Disability Index, sleep quality with Pittsburgh Sleep Quality Index will be evaluated before and after treatment. All parameters will be compared between ET and ET+NMES group.
Investigators
Ebru Kaya Mutlu, PT
Associate Prof. Dr, PhD
Istanbul University - Cerrahpasa (IUC)
Eligibility Criteria
Inclusion Criteria
- •Having a diagnosis of subacute / chronic extrinsic SIS
- •18 to 65 years of age
- •Being volunteer
Exclusion Criteria
- •Fracture or surgical history in the shoulder region
- •Another diagnosis that can affect shoulder function
- •Having received local corticosteroid injection / treatment in the shoulder joint within the last 3 months
- •Neuromuscular disease
- •Pregnancy
- •Unstabil angina
- •Communication problems
- •Systemic inflammatory joint disease
- •Situations where electrical stimulation and exercise are contraindicated
- •Orthopedic, rheumatologic or congenital disease of the affected upper extremity
Outcomes
Primary Outcomes
Disability Arm Shoulder Hand Questionnaire (DASH)
Time Frame: 8 weeks
The DASH questionnaire is a region-specific, self-report scale to evaluate health status of upper extremity disabilities.
Secondary Outcomes
- Pittsburgh Sleep Quality Scale(8 weeks)
- Goniometer(8 weeks)
- Neck Disability Index(8 weeks)
- Visual Analog Scale (VAS)(8 weeks)
- Digital hand-held dynamometer(8 weeks)