Lifestyle changes for African-American breast cancer survivors
Developing FIM-BCS: A Lifestyle Modification for African-American Breast Cancer Survivors With Cardiovascular Risk Factors
NA · University of Illinois at Chicago · NCT06504914
This study is trying out a 12-week program that includes grocery delivery and cooking classes to see if it can help Black women with high blood pressure and obesity eat healthier and improve their health.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 24 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | Female |
| Sponsor | University of Illinois at Chicago (other) |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT06504914 on ClinicalTrials.gov |
What this trial studies
This study examines the feasibility and acceptability of a 12-week intervention called RN-CHeFRx, which includes grocery delivery, cooking classes, and nutrition education, aimed at improving dietary habits and blood pressure control among Black women with hypertension and obesity. The intervention will be piloted with 20 participants who meet specific health criteria, and their blood pressure, BMI, and sodium intake will be assessed at baseline, 12 weeks, and 6 months. The findings will help inform a larger clinical trial focused on enhancing health outcomes for this population.
Who should consider this trial
Good fit: Ideal candidates for this study are Black women aged 18 and older who are obese and have hypertension.
Not a fit: Patients who are currently undergoing cancer treatment or have significant cognitive deficits may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could lead to improved dietary habits and better blood pressure control for African-American women with hypertension and obesity.
How similar studies have performed: Other studies have shown success with lifestyle modification interventions targeting similar populations, indicating potential for positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * self-identified as Black or of African descent * female * ≥ 18 years old * baseline blood pressure ≥130/85 or diagnosed with hypertension and/or BMI ≥ 25 Exclusion Criteria: * inability to cook in their homes * cognitive deficits impeding the ability to participate or provide informed consent * current treatment for cancer * liver or renal disease * pregnancy * lack of English language proficiency
Where this trial is running
Chicago, Illinois
- University of Illinois Chicago — Chicago, Illinois, United States (RECRUITING)
Study contacts
- Study coordinator: Saria Lofton
- Email: slofto4@uic.edu
- Phone: 312-355-2125
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.
Conditions: Hypertension, Obesity, Nutrition, Healthy