RECRUITING

Enhancing the Effectiveness of Home-delivery Based Produce Prescription Program Implementation Strategies

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

Harris Health System is currently participating, along with two other partners, GoldiFresh Inc., and Brighter Bites, in a cross-sector collaborative home delivery-based Produce Prescription Program (PPRx) pilot initiative that provides consistent access to healthy food plus nutrition education to Medicaid-eligible pregnant women in Harris County, TX, deemed to be at high risk of adverse pregnancy or birth outcomes. The objectives of this study are two-fold: (a) to examine utilization of food basket contents and improvements in diet quality in this home delivery based PPRx program, and (b) to evaluate if and the extent to which utilization of food basket contents outcomes improves with support from an interactive AI-based conversational agent to convert food into healthy meals.

Official Title

Enhancing the Effectiveness of Home-delivery Based Produce Prescription Program Implementation Strategies

Quick Facts

Study Start:2024-07-26
Study Completion:2025-11-25
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06114199

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 44 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * receiving prenatal care at high-risk obstetric clinics
  2. * \<= 20 weeks medically-confirmed viable pregnancy
  3. * designated as high risk \[Age\>=35 years, or obese or overweight (BMI\>=25.0 at pre pregnancy self-report), or prior history of pregnancy hypertension or gestational diabetes\]
  4. * within the zip code delivery radius
  1. * women who were medically recommended bed rest through pregnancy
  2. * substance users

Contacts and Locations

Study Contact

Nalini Ranjit, PhD
CONTACT
(512) 391-2527
Nalini.Ranjit@uth.tmc.edu

Principal Investigator

Nanlini Ranjit, PhD
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Nanlini Ranjit, PhD, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

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 Date2024-07-26
Study Completion Date2025-11-25

Study Record Updates

Study Start Date2024-07-26
Study Completion Date2025-11-25

Terms related to this study

Additional Relevant MeSH Terms

  • Nutritional Deficiency in Pregnancy