Actively Recruiting
Subacromial Impingement Syndrome: The Relationship Between Shoulder Functional Tests and Ultrasound Parameters
Led by Muğla Sıtkı Koçman University · Updated on 2024-09-25
70
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients diagnosed with subacromial impingement syndrome, a common cause of shoulder pain. The study focuses on understanding how shoulder functional tests relate to ultrasound measurements. Patients are selected based on clinical evaluations like Neer's test, Hawkins Kennedy, and supraspinatus palpation test, with age limits between 18 and 70 years. The study is observational and conducted at a Physical Medicine and Rehabilitation outpatient clinic. Participants will undergo diagnostic evaluations where demographic data is collected, and shoulder function is assessed using DASH and Constant Murley scores. A radiologist with four years of musculoskeletal ultrasound experience will measure subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, and the ratio of tendon thickness to acromiohumeral distance using a Siemens V8 ultrasound device in a specific arm position. During the study visit, patients will have their demographic information recorded and complete the functional scores. Ultrasound measurements will be taken to assess shoulder structures. Researchers will analyze these data to evaluate the relationship between functional test results and ultrasound parameters. The main outcomes measured on the study day include subacromial bursa thickness, supraspinatus tendon thickness, and acromiohumeral distance.
CONDITIONS
Brief Title
Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Being between 18 and 70 years old
- Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)
You will not qualify if you...
- Under 18 or over 70 years of age
- Diagnosed with rheumatologic diseases
- Symptomatic shoulder osteoarthritis
- Shoulder instability
- Shoulder pain during active or passive cervical spine movements
- Previous shoulder surgery
- Findings of adhesive capsulitis (more than 50% restriction of passive range of motion in 2 planes or full-thickness rotator cuff tear on ultrasound)
- Received physiotherapy or intra-articular injection in the last 3 months
- Diagnosis of type 2 diabetes or hypothyroidism
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo shoulder functional tests and ultrasound measurements including subacromial bursa thickness, supraspinatus tendon thickness, and acromiohumeral distance.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Mugla Egitim Arastima
Muğla, Turkey (Türkiye)
Actively Recruiting
Research Team
N
Nihal KARAYER OZGUL, 1
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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