Is sarcopenia a risk factor for rotator cuff tears?
Nicolás A Atala, Santiago L Bongiovanni, Ana M Galich...
https://pubmed.ncbi.nlm.nih.gov/33157241Actively Recruiting
Led by Haydarpasa Numune Training and Research Hospital · Updated on 2025-11-26
104
Participants Needed
1
Research Sites
4 weeks
Total Duration
Sarcopenia, the loss of muscle mass due to aging, can lead to reduced muscle function and increased risks such as falls and fractures. This research aims to explore whether sarcopenia is linked to rotator cuff tears in patients diagnosed with rotator cuff syndrome, and to identify the location and type of these tears. The study focuses on adults aged 40 to 75 years who experience shoulder pain lasting at least three months and have undergone shoulder MRI as part of their diagnosis. Participants will undergo assessments for sarcopenia using the STAR (Sonographic Thigh Adjustment Ratio) method, which includes measuring gait speed, handgrip strength, chair stand test time, and anterior thigh muscle thickness via ultrasound. Patients will be categorized as non-sarcopenic, pre-sarcopenic, or sarcopenic based on these evaluations. Their shoulder MRIs will then be analyzed to determine the presence, type, and severity of rotator cuff tears. Throughout the study, demographic and clinical data will be collected, including pain severity using the Visual Analog Scale and shoulder function via the Shoulder Disability Questionnaire. Sarcopenia assessments and shoulder MRI analyses will be conducted independently to ensure unbiased results. The primary outcome is the STAR value at baseline, with secondary outcomes including detailed radiologic evaluation of shoulder MRIs. Participation involves clinical assessments, physical tests, ultrasound measurements, and review of imaging to better understand the relationship between sarcopenia and rotator cuff tears.
CONDITIONS
Does Sarcopenia Influence Rotator Cuff Tear Patterns? Radiological Insights From Patients With Rotator Cuff Syndrome
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single session
Participants undergo clinical assessment for rotator cuff syndrome including shoulder pain evaluation and functional impairment assessment. Sarcopenia is assessed using gait speed, handgrip strength, chair stand test, and ultrasonographic measurement of anterior thigh muscle thickness.
1 visit (in-person)
Duration - Up to study completion
Participants’ shoulder MRI scans are analyzed to assess rotator cuff tear presence, type, and severity, correlating these findings with sarcopenia status.
No additional visits required
Total: 1 location
1
Health Science University Haydarpaşa Numune Research and Training Hospital
Istanbul, Üsküdar, Turkey (Türkiye), 34668
Actively Recruiting
S
sibel Suzen Ozbayrak, M.D.
E
Elem Yorulmaz, M.D.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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