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NCT06407284Not yet recruiting

Brighter Bites/Legacy Produce Rx Program

Brighter Bites & Legacy Community Health Produce Rx: Evaluating the Feasibility and Effectiveness of a School-based Clinical Nutrition Program With Produce Prescription

Source: ClinicalTrials.gov · Last updated 10 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to assess the effectiveness of the produce prescription program at improving weight status and obesity-related health outcomes of participants, to examine the impacts of the program on household food insecurity and nutrition security, to examine the impacts of the program on participating adolescents' dietary behavioral outcomes, their home nutrition environment and feeding practices and to examine the impacts of the program in reducing healthcare use and associated costs

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
600 (estimated)
First submitted
6 May 2024
Start date
15 Jan 2025
Primary completion date
30 Jun 2026
Lead sponsor
The University of Texas Health Science Center, Houston
Diseases
Obesity
NCT number
NCT06407284

What you commit to

  • Study type: Interventional
  • Planned participants: 600
  • From 15 Jan 2025 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • currently participating in Brighter Bites
  • with a family member/sibling currently participating in Brighter Bites

Who the study is looking for

  • Must be a patient at one of the four Legacy Community Health School-based clinics in Galena Park, Texas
  • BMI greater than or equal to 85th percentile
  • reside within a 10-mile radius of Houston Food Bank
  • Medicaid recipients or low-income uninsured
  • parents must be able to read and write in English or Spanish to complete surveys
  • patient and parents must confirm their willingness to complete the participant's well-child visit for the entire period of the study (approximately one year).

Age in the registry: 12 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Texas Health Science Center at Houston
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.