Actively Recruiting
Shoulder and Neck Mobilization in Patients With Subacromial Impingement Syndrome
Led by Kutahya Health Sciences University · Updated on 2024-10-10
45
Participants Needed
1
Research Sites
99 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Patients who come to Tavşanlı State Hospital's Physical Therapy and Rehabilitation Department and have been diagnosed with subacromial impingement syndrome by a physician will be included. Patients will be selected by randomization method among the patients determined by the physician to receive conservative treatment, shoulder mobilization in addition to conservative treatment, and neck mobilization treatment program in addition to these. Conventional treatments such as hot packs, TENS, ultrasound, and exercise will be given to all patients by the hospital staff. Pain intensity will be evaluated with VAS. Additionally, painful arch and pain-free joint range of motion evaluation will be made using a goniometer. The DASH questionnaire will be used to evaluate shoulder functionality. Sensory evaluation will be made with pressure pain threshold and two-point discrimination tests. Measurements will be made before the intervention and repeated after 3 weeks of intervention.
CONDITIONS
Official Title
Shoulder and Neck Mobilization in Patients With Subacromial Impingement Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Being over 18 years of age
- Diagnosed with Subacromial Impingement
- Not having received any treatment for shoulder problems in the last 6 months
- The pain has been continuing for 3 months
- Initial pain must be 4 or higher on the Visual Analog Scale (VAS)
You will not qualify if you...
- History of surgery in the shoulder, cervical and thoracic region
- Having a shoulder problem such as a frozen shoulder or instability
- Full-thickness rotator cuff tear
- Having systemic musculoskeletal disease
- Having systemic rheumatic disease
- History of upper extremity fracture
- Diagnosed with scoliosis
- Have neurological problems
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kutahya Health Sciences University
Kütahya, Turkey (Türkiye), 43100
Actively Recruiting
Research Team
M
Meltem Işıntaş
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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