RECRUITING

Preparing FIM-BCS - A Lifestyle Modification for African-American Breast Cancer Survivors

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Hypertension and obesity are both major risk factors for cardiovascular disease (CVD), a leading cause of death for Black women in the United States. The investigators propose examining the feasibility and acceptability of the 12-week RN-CHeFRx (Real Nourishment and Cooking Healthy Food is Rx) intervention \- grocery delivery, cooking classes, and nutrition education - for Black women with hypertension and obesity to improve nutritious eating habits and blood pressure control.

Official Title

Developing FIM-BCS: A Lifestyle Modification for African-American Breast Cancer Survivors With Cardiovascular Risk Factors

Quick Facts

Study Start:2024-02-05
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06504914

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * self-identified as Black or of African descent
  2. * female
  3. * ≥ 18 years old
  4. * baseline blood pressure ≥130/85 or diagnosed with hypertension and/or BMI ≥ 25
  1. * inability to cook in their homes
  2. * cognitive deficits impeding the ability to participate or provide informed consent
  3. * current treatment for cancer
  4. * liver or renal disease
  5. * pregnancy
  6. * lack of English language proficiency

Contacts and Locations

Study Contact

Saria Lofton
CONTACT
312-355-2125
slofto4@uic.edu

Study Locations (Sites)

University of Illinois Chicago
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: University of Illinois at Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-05
Study Completion Date2026-06

Study Record Updates

Study Start Date2024-02-05
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Hypertension
  • Obesity
  • Nutrition, Healthy