Subacromial Impingement Syndrome Functional Tests Correlation With Ultrasound Parameters

NCT06384430 | Recruiting DMC

• 1 other identifier: MuğlaSKU-NKO
• Study Type: observational
• Target: 70
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Subacromial Impingement Syndrome; Shoulder Tendinitis; Shoulder Bursitis; Shoulder Pain

Outcome Measures

Primary Outcomes (3)

• subacromial bursa thickness

  subacromial bursa thickness measure

  1 day

• supraspinatus tendon thickness

  supraspinatus tendon thickness measure

  1 day

• acromiohumeral distance

  acromiohumeral distance measure

  1 day

Study Arms (1)

Patients with subacromial impingement syndrome

Patients with subacromial impingement syndrome: Being between 18-70 years old Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)

Diagnostic Test: Shoulder functional tests and ultrasound

Interventions

Shoulder functional tests and ultrasound DIAGNOSTIC_TEST

On the day of the study, demographic data will be collected from patients with a clinical diagnosis of impingement and who agree to participate in the study, then DASH and Constant Murley scores will be calculated and subacromial bursa thickness, supraspinatus tendon thickness, acromiohumeral distance, supraspinatus tendon thickness/acromiohumeral distance ratio will be calculated on ultrasound.

Patients with subacromial impingement syndrome

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Being between 18-70 years old and clinical evaluation positive for subacromial impingement syndrome.

You may qualify if:

• Being between 18-70 years old
• Clinical evaluation positive for subacromial impingement syndrome (Neer's test, Hawkins Kennedy, supraspinatus palpation test)

You may not qualify if:

• Under 18, over 70 years of age
• Those diagnosed with rheumatologic diseases
• Those with symptomatic shoulder osteoarthritis
• Those with shoulder instability
• Shoulder pain in active, passive cervical spine movements
• Previous shoulder surgery
• Findings of adhesive capsulitis (\>50% restriction of passive range of motion in 2 planes or detection of a full-thickness rotator cuff tear on ultrasound)
• Physiotherapy or intra-articular injection in the last 3 months
• Diagnosis of type 2 diabetes or hypothyroidism

Sponsors & Collaborators

• Muğla Sıtkı Koçman University: lead

Study Sites (1)

Mugla Egitim Arastima

Muğla, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Shoulder Impingement Syndrome; Shoulder Pain

Interventions

Ultrasonography

Condition Hierarchy (Ancestors)

Joint Diseases; Musculoskeletal Diseases; Shoulder Injuries; Wounds and Injuries; Arthralgia; Pain; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Diagnostic Imaging; Diagnostic Techniques and Procedures; Diagnosis

Central Study Contacts

Nihal KARAYER OZGUL, 1

CONTACT

+905073068312; nihalkarayer505@gmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Target Duration: 1 Day
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: April 22, 2024
• First Posted: April 25, 2024
• Study Start: April 1, 2024
• Primary Completion: September 30, 2024
• Study Completion: October 31, 2024
• Last Updated: September 25, 2024

Record last verified: 2024-09

Locations

TU (1)