Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06818669

Cardiovascular Risk Reduction for Adults With Food Insecurity Using Structured Incentives

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University at Buffalo

Buffalo, New York, 14203, United States

Location status: Recruiting

Location contact

Rebekah J Walker, PhD

CONTACT

[email protected]

716-829-5741

About this study

Study Overview: 200 African American adults at risk for CVD with food insecurity will be randomized 1:1 to CVD-FIT or enhanced usual care (CVD risk reduction education). Each patient will be followed for 12 months, with study visits at baseline, 3, 6, and 12 months. The primary outcome will be 10-year CVD risk using the Pooled Cohort Equation at 12 months post-randomization while the secondary outcomes will be quality of life at 12 months post-randomization and cost-effectiveness of the CVD-FIT intervention compared to enhanced usual care.

Patient Randomization. A permuted block randomization method will be used to assign subjects to intervention or control. All subjects who are randomized will be entered into the study database and analyzed according to CONSORT guidelines.

Description of the CVD-FIT Intervention: The CVD-FIT intervention will incorporate 1) $100 monthly income supplementation; 2) $50 weekly structured incentive for the purchase of healthy food options; and 3) evidence-based telephone delivered CVD risk reduction education and skills training.

Enhanced Usual Care Control Group: Participants randomized to the enhanced usual care group will receive the same mailed education and health educator delivered education and skills training sessions as the CVD-FIT intervention group.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • self-report as African American/non-Hispanic Black
  • 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)
  • 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
  • able to communicate in English.

Exclusion criteria

  • Mental confusion on interview suggesting significant dementia
  • Participation in other cardiovascular disease clinical trials
  • Alcohol or drug abuse/dependency based on screening using CAGE questionnaire
  • Active psychosis or acute mental disorder based on self-report
  • Life expectancy <12 months.

Treatment and study plan

CVD-FIT

Behavioral

The structured incentive will include monthly supplemental income plus weekly reimbursement for the purchase of healthy food options. Education for CVD risk reduction will include mailed education and telephone calls with a trained health educator.

Enhanced Usual Care

Behavioral

Education for CVD risk reduction will include mailed education and telephone calls with a trained health educator.

Primary outcomes

  1. 10-Year CVD Risk

    Time frame: baseline, 3-months, 6-months, and 12-months post randomization

    10-year CVD risk will be measured by the Pooled Cohort risk reduction equation recommended for race- and sex- specific risk calculation for African Americans 40 to 79 years of age.

  2. CVD Risk - PREVENT

    Time frame: baseline, 3-months, 6-months, and 12-months post randomization

    CVD Risk will be measured using the PREVENT equation

Secondary outcomes

  1. Physical and Mental Health Related Quality of Life

    Time frame: baseline, 3-months, 6-months, and 12-months post randomization

    Quality of Life will be measured using the SF-12 questionnaire and reported as physical health related and mental health related scores (score ranges from 0 to 100 with higher numbers indicating better quality of life)

Study contacts

Contact information is provided by the study sponsor or research team.

Jocelyn Stooks, MPH

CONTACT

[email protected]

716-829-2364

Rebekah J Walker, PhD

CONTACT

[email protected]

716-829-5741

Sponsors and collaborators

Lead sponsor

State University of New York at Buffalo

Other

Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

Registry information

Official study title

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

Acronym: CVD-FIT

Important dates

Study start
2025
Primary completion
2030
Study completion
2031
First posted
Feb 10, 2025
Registry last updated
Feb 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.