COMPLETED

Comparing the Effectiveness of Two Produce Prescription Approaches On Fruit and Vegetable Intake and Food Security, While Exploring Implementation Outcomes Such as Reach, Implementation, Sustainability, and Cost

Conditions

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 produce prescription program is one type of food is medicine (FIM) programs, where healthcare providers "prescribe" fruits and vegetables (F\&V) to patients with low household incomes, experience food insecurity, and one or more diet-related diseases. NutriConnect seeks to compare the effectiveness of two produce prescription approaches on F\&V intake and food security: credit to Rewards account (NutriConnect Credit) vs. produce box delivery (NutriConnect Delivery), while exploring implementation outcomes such as reach, sustainability, implementation, and cost.

Official Title

NutriConnect: Enhancing Health and Food Security Through Sustainable Solutions and Partnerships

Quick Facts

Study Start:2024-03-25
Study Completion:2025-10-23
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06263751

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 to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Adults (\>= 18 years)
  2. 2. Received care at either medical floors or observation unit at the Bares Jewish Hospital (BJH), and discharged to home.
  3. 3. Being screened positive for food or financial insecurity.
  4. 4. Have elevated cardiovascular risk, i.e., self-reported diabetes, hypertension, hyperglycemia, or calculated BMI meeting obesity.
  1. 1. Does not have competence to provide informed consent.
  2. 2. Is under suicide watch.
  3. 3. Is in police custody.
  4. 4. In hospice or palliative care.
  5. 5. Not have a stable home.
  6. 6. Is pregnant.

Contacts and Locations

Principal Investigator

Jing Li, MD, DrPH, MS
PRINCIPAL_INVESTIGATOR
Washington University School of Medicine

Study Locations (Sites)

Barnes Jewish Hospital
St Louis, Missouri, 63110
United States

Collaborators and Investigators

Sponsor: Washington University School of Medicine

  • Jing Li, MD, DrPH, MS, PRINCIPAL_INVESTIGATOR, Washington University School of Medicine

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 Date2024-03-25
Study Completion Date2025-10-23

Study Record Updates

Study Start Date2024-03-25
Study Completion Date2025-10-23

Terms related to this study

Additional Relevant MeSH Terms

  • Food Insecurity