Examining sleep issues in Somali Americans
Disrupted Sleep in Somali Americans - Implications for Hypertension Risk
This study is trying to understand sleep problems in healthy Somali Americans and see how these issues might be linked to high blood pressure and other factors.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 240 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Trial ID | NCT05411029 on ClinicalTrials.gov |
What this trial studies
This observational study aims to identify the types and severity of undiagnosed sleep deficiencies in healthy Somali Americans. It will utilize 24-hour blood pressure monitoring and polysomnography to explore the relationship between sleep deficiencies and increased blood pressure. The study will also investigate psychosocial, behavioral, environmental, and biological factors that may contribute to these sleep issues. By focusing on this specific population, the research seeks to provide insights into the unique challenges faced by Somali Americans regarding sleep health.
Who should consider this trial
Good fit: Ideal candidates for this study are Somali Americans aged 18 to 70 who have no known history of hypertension, diabetes, or sleep disorders.
Not a fit: Patients under 18 years, over 70 years, or those who are pregnant may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better understanding and management of sleep disorders and hypertension in Somali Americans.
How similar studies have performed: While there may be studies on sleep disorders and hypertension, this specific focus on Somali Americans is relatively novel and underexplored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subjects diagnosed with no known history of hypertension, diabetes, or sleep disorders. * Self-identify as Somali. * Adult males and females who are older than 18 years of age. Exclusion Criteria: * Anyone under 18 years or over 70 years. * Positive pregnancy.
Where this trial is running
Rochester, Minnesota
- Mayo Clinic in Rochester — Rochester, Minnesota, United States (Recruiting)
Study contacts
- Principal investigator: Virend Somers, MD — Mayo Clinic
- Study coordinator: Somers CPL Lab
- Email: CPLSOMALI@mayo.edu
- Phone: 507-422-3499
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.