Actively Recruiting
FRESH-EATS Project
Led by University of South Florida · Updated on 2025-07-08
48
Participants Needed
1
Research Sites
71 weeks
Total Duration
On this page
Sponsors
U
University of South Florida
Lead Sponsor
N
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this randomized controlled trial is to determine the feasibility of the FRESH-EATS project in children ages 8-12 and their parents/caregivers residing in low-income, predominantly minority neighborhoods. The main questions it aims to answer are: Is the FRESH-EATS intervention feasible to implement and well-received by parent-child dyads? Does the FRESH-EATS multilevel multicomponent intervention improve dietary behaviors of children and their parents/caregivers compared to the comparison group? We hypothesize that this innovative community-derived, multilevel-multicomponent intervention is feasible to implement and has the potential to improve dietary behaviors of participants (children ages 8-12 and their parents/caregivers). Researchers will compare the FRESH-EATS intervention group to the Lagged Intervention Control Group (LICG) to see if the FRESH-EATS intervention leads to better dietary behaviors and health outcomes. Participants in the FRESH-EATS intervention group will: * Attend educational sessions on healthy eating and cooking. * Participate in family workshops that address access to healthy food. * Receive food deliveries and information about local food resources. * Engage in community garden activities.
CONDITIONS
Official Title
FRESH-EATS Project
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Speak English
- Be a parent or caregiver aged 18 years or older
- Live in the targeted neighborhood
- Have a child aged 8 to 12 years old
You will not qualify if you...
- Parents/caregivers or children who have participated in a similar intervention within the past 6 months
- Do not speak English
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of South Florida
Tampa, Florida, United States, 33620
Actively Recruiting
Research Team
H
Heewon L. Gray, PhD, RDN
CONTACT
M
Marilyn Stern, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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