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NCT07218588Completed

Sanctuary Farm Prescription in Adolescents

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

The goal of this research study is to learn if an 8-week produce prescription program (in partnership with a local urban farm) can increase fruit and vegetable consumption in overweight teens and improve their blood pressure and weight. The main questions are: * Is a produce prescription program in overweight teens feasible? * Will a produce prescription with educational videos increase weekly fruit and vegetable intake? * Will a produce prescription with educational videos improve blood pressure and weight for height? Researchers will compare the teens' fruit and vegetable intake, blood pressure and weight for height before and after the produce prescription. Researchers will also see how feasible it is by measuring the number of produce prescriptions are picked up by the families and how many educational videos are viewed. Participants will: * complete questionnaires related to their diet and nutrition * measure their blood pressure and weight at the beginning and end of the study * obtain weekly produce prescriptions

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
16 Oct 2025
Start date
20 Nov 2025
Primary completion date
30 Jun 2026
Lead sponsor
Nemours Children's Clinic
Diseases
Obesity
NCT number
NCT07218588

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 20 Nov 2025 to the primary completion date, 30 Jun 2026
  • 3 sites 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.

Criteria the registry did not label

  • Inclusion
  • Patients seen at Nemours TJU Primary Care Clinic
  • Ages 12-17 years at enrollment
  • BMI \> or = 85th percentile
  • English Speaking
  • Willing to provide parental permission and ability to provide child assent for the study
    • Exclusion
  • Children with neurocognitive delays that would limit participation or ability to assent
  • Use of G-tube/J-tube
  • Food allergies that in the opinion of the investigators would interfere with ability to participate.

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

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
Thomas Jefferson University
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Nemours Children's Health
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Nemours Children's Hospital, DE
Coordinator of this site? Confirm its status
WilmingtonUnited StatesUnknown status

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