Exercise training for improving health in patients with obesity hypoventilation syndrome
Effects of Exercise Training on Exercise Capacity and Sleep Quality in Patients With Obesity Hypoventilation Syndrome
This study is testing if a 10-week exercise program can help people with Obesity Hypoventilation Syndrome improve their ability to exercise and sleep better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Istanbul University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT05398068 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of aerobic and strength training on exercise capacity and sleep quality in patients diagnosed with Obesity Hypoventilation Syndrome (OHS). Patients will be randomly assigned to either an exercise intervention group or a control group and will undergo a 10-week exercise program. Assessments will include the Six-Minute Walking Test, Pittsburgh Sleep Quality Index, and evaluations of muscle strength and quality of life. The goal is to determine how exercise impacts various health parameters in individuals suffering from OHS.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old diagnosed with Obesity Hypoventilation Syndrome.
Not a fit: Patients with uncontrolled respiratory diseases or other serious comorbid conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve exercise capacity and sleep quality for patients with obesity hypoventilation syndrome.
How similar studies have performed: While the specific effects of exercise on OHS are not well-documented, similar studies in related respiratory conditions have shown positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * \>18 years old * Patients who have been diagnosed with Obesity Hypoventilation Syndrome Exclusion Criteria: * Patients who participate in any other diet program * Patients who are incompatible with a diet program or exercise program * Patients with uncontrollable respiratory and comorbid diseases * Patient who have been an orthopedic, neurological, cardiac, or metabolic condition that may prevent participation and continuation of the exercise program throughout the study
Where this trial is running
Istanbul
- Istanbul University-Cerrahpasa — Istanbul, Turkey (Recruiting)
Study contacts
- Study coordinator: Goksen Kuran Aslan, Assoc. Prof.
- Email: goksenkuran@yahoo.com
- Phone: +90 (212) 414 15 28
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.