Actively Recruiting
Evaluation of Sarcopenia and Associated Factors in Patients with Lipedema
Led by Dokuz Eylul University · Updated on 2025-03-12
102
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the relationship between sarcopenia, a condition involving age-related loss of muscle mass and strength, and lipedema, a chronic condition affecting women characterized by abnormal fat buildup and pain in the legs and sometimes arms. The study aims to understand whether muscle weakness in lipedema patients is part of the disease or a result of decreased activity and to explore how factors like age, body mass index, exercise, lipedema type, and stage relate to muscle loss. This research addresses an important gap as sarcopenia has not been studied in lipedema patients before. The study involves two groups: women aged 18 to 85 diagnosed with lipedema, and healthy volunteers in a similar age range without lipedema. Participants will undergo diagnostic tests including ultrasound measurement of thigh muscle thickness to calculate the STAR (Sonographic Thigh Adjustment Ratio), hand grip strength tests, a chair stand test, and walking speed assessment to evaluate muscle mass and function. These tests help identify sarcopenia and assess physical performance. During the study visit, participants will have muscle thickness measured by ultrasound, perform hand grip strength tests using a dynamometer, complete a 5-repeat chair stand test, and walk a 6-meter course to measure gait speed. Researchers will analyze these results to assess muscle loss and function. The study is observational and does not involve treatment interventions. Participants will be monitored for these measures on a single day, and the study aims to improve understanding of sarcopenia in women with lipedema to support better conservative management strategies.
CONDITIONS
Brief Title
Sarcopenia and Related Factors in Lipedema
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between the ages of 18 and 85
- Diagnosed with lipedema
- Agree to participate in the study
- Have a sociocultural level suitable for participation
- Healthy volunteers of similar age for the control group
You will not qualify if you...
- Have chronic venous insufficiency and/or lymphedema
- Have Parkinson's disease, previous stroke, cerebellar diseases, multiple sclerosis, major depression, neuromuscular diseases, history of major orthopedic surgery, severe hip or knee osteoarthritis, rheumatological diseases, malignancies, advanced heart, liver or renal failure, visual impairment, or vestibular diseases
- Use any assistive device to walk
- Are illiterate or have cognitive impairment preventing written consent
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.
1 visit (in-person)
Duration - 1 day
Participants undergo diagnostic tests including ultrasonography to measure anterior thigh muscle thickness, hand grip strength measurement, chair stand test, and 6 meter gait speed assessment to evaluate sarcopenia and muscle function.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Department of Physical Medicine and Rehabilitation, Medical Faculty of Dokuz Eylül University, İzmir, Turkey
Izmir, Turkey (Türkiye)
Actively Recruiting
Research Team
N
Nihan Erdinc Gunduz, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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