Effects of exercise training on lipedema in women
The Effects of Endurance Training in Women With Lipedema
This study is testing if an 8-week high-intensity exercise program can help women with lipedema feel better and manage their symptoms.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Norwegian University of Science and Technology Academic / other |
| Locations | 1 site (Trondheim) |
| Trial ID | NCT05488977 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of an 8-week high-intensity interval training (HIIT) program on women diagnosed with lipedema, a condition characterized by painful fat accumulation in the limbs. Thirty participants aged 18-65 will be randomly assigned to either the exercise group or a control group. The exercise regimen consists of supervised sessions twice a week, focusing on intervals that elevate heart rates significantly. Data will be collected on participants' lipedema characteristics and their use of clinical aids throughout the study.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18-65 who have been diagnosed with lipedema and can participate in supervised exercise training.
Not a fit: Patients with ongoing eating disorders or orthopedic limitations that prevent them from engaging in exercise training may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a new, effective exercise-based intervention for managing lipedema symptoms and improving quality of life for affected women.
How similar studies have performed: While few studies have explored exercise training for lipedema, existing guidelines suggest that physical activity is beneficial, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: - can meet for supervised exercise training in Trondheim. Exclusion Criteria: * eating disorders and/or orthopedic limitations for exercise training
Where this trial is running
Trondheim
- Institute for Circulation and Medical Imaging, NTNU — Trondheim, Norway (Recruiting)
Study contacts
- Study coordinator: Anja Bye
- Email: anja.bye@ntnu.no
- Phone: +4793232057
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.