Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorMuğla Sıtkı Koçman University

About this trial

In this study, among the patients who applied to the Physical Medicine and Rehabilitation outpatient clinic of Muğla Training and Research Hospital and were diagnosed with subacromial impingement by anamnesis and clinical tests, inclusion criteria) and exclusion criteria will be included in the study. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated. 4 years of musculoskeletal ultrasound experience will be recorded by a radiologist using ultrasound (Siemens® V8, LA2-14A probe) in modified Crass position (positioning with the palm of the examined side on the posterior iliac wing) by measuring subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness/acromiohumeral distance ratio. Demographic data of the patients will then be recorded. DASH (Disabilities of the Arm, Shoulder and Hand) and Constant Murley scores will be calculated.

Eligibility criteria

Qualifiers

Being between 18-70 years old

Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)

Disqualifiers

Under 18, over 70 years of age

Those diagnosed with rheumatologic diseases

Those with symptomatic shoulder osteoarthritis

Those with shoulder instability

Trial design

Treatments tested in this trial

  • Shoulder functional tests and ultrasound

Treatment groups

70 Participants
are divided into 1 treatment group