RECRUITING

Cardiovascular Risk Reduction for Adults With Food Insecurity Using Structured Incentives

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

The overarching aim of this proposal is to test the efficacy and cost-effectiveness of CVD-FIT, a novel, multi-component intervention that includes three components: 1) monthly income supplementation; 2) weekly structured incentive for the purchase of healthy food options; and 3) evidence-based telephone delivered CVD risk reduction education and skills training in African Americans with food insecurity.

Official Title

Cardiovascular Risk Reduction for Adults With Food Insecurity Using Structured Incentives (CVD-FIT)

Quick Facts

Study Start:2025-05-01
Study Completion:2030-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06818669

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * self-report as African American/non-Hispanic Black
  2. * screen positive for food insecurity over the past 12-months using a food insecurity risk tool developed through completion of the research team's current NIH funded R01 (R01MD013826)
  3. * at risk for CVD defined as age ≥40 years and having a clinical diagnosis of diabetes, or hypertension, or hyperlipidemia, or being overweight/obese (defined as a BMI\>25), or being a current smoker
  4. * able to communicate in English.
  1. * Mental confusion on interview suggesting significant dementia
  2. * Participation in other cardiovascular disease clinical trials
  3. * Alcohol or drug abuse/dependency based on screening using CAGE questionnaire
  4. * Active psychosis or acute mental disorder based on self-report
  5. * Life expectancy \<12 months.

Contacts and Locations

Study Contact

Rebekah J Walker, PhD
CONTACT
716-829-5741
rbwalker@buffalo.edu
Jocelyn Stooks, MPH
CONTACT
716-829-2364
jstooks@buffalo.edu

Study Locations (Sites)

University at Buffalo
Buffalo, New York, 14203
United States

Collaborators and Investigators

Sponsor: State University of New York at Buffalo

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 Date2025-05-01
Study Completion Date2030-03

Study Record Updates

Study Start Date2025-05-01
Study Completion Date2030-03

Terms related to this study

Keywords Provided by Researchers

  • Food Insecurity
  • Financial Incentives

Additional Relevant MeSH Terms

  • Cardiovascular Diseases