Investigating muscle strength and function in women with lipedema
Evaluation of Sarcopenia and Associated Factors in Patients with Lipedema
This study is trying to see how muscle strength and function are affected in women with lipedema compared to healthy women.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 102 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | Female |
| Sponsor | Dokuz Eylul University Academic / other |
| Drugs / interventions | CART |
| Locations | 1 site (Izmir) |
| Trial ID | NCT05739279 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between sarcopenia and muscle strength in women diagnosed with lipedema. It will assess various factors such as hand grip strength, chair stand test results, and gait speed to understand how these elements interact with the condition. By identifying potential sarcopenia and functional limitations, the study seeks to enhance the understanding of physical activity participation among affected individuals. The research will involve participants aged 18-85, including both those with lipedema and healthy volunteers for comparison.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18-85 diagnosed with lipedema.
Not a fit: Patients with chronic venous insufficiency, lymphedema, or significant neurological and orthopedic conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for women with lipedema, enhancing their physical activity and quality of life.
How similar studies have performed: While the relationship between sarcopenia and lipedema has not been previously investigated, studies on sarcopenia in other populations have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * between the ages of 18-85 * with a diagnosis of lipoedema * who agreed to participate in the study * having a sociocultural level suitable for participation in the study * healthy volunteers in a similar age group for the control group Exclusion Criteria: * with chronic venous insufficiency and/or lymphedema * with Parkinson's disease, previous stroke, cerebellar diseases, multiple sclerosis, major depression, neuromuscular diseases, history of major orthopedic surgery, severe hip/knee osteoarthritis, rheumatological diseases, malignancies, advanced heart/liver/renal failure, visual impairment, and vestibular diseases, and those who use any assistive device to walk * who are illiterate and have cognitive impairment that will prevent them from giving written consent will not be included in the study
Where this trial is running
Izmir
- Department of Physical Medicine and Rehabilitation, Medical Faculty of Dokuz Eylül University, İzmir, Turkey — Izmir, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Nihan Erdinc Gunduz, M.D.
- Email: nihanerdinc@gmail.com
- Phone: +905063992614
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.