Feasibility of Online-supported Delivery Bringing Optimal Nutrition to Diverse Low-income Households With Children (FOODBOX)

January 30, 2026 updated by: Cornell University

Program Evaluation of FOODBOX: "Feasibility of Online-supported Delivery Bringing Optimal Nutrition to Diverse Low-income Households With Children

The goal of this study is to find ways to help families with children who have limited incomes get better access to healthy and culturally appropriate foods. The study will test a program called "medically tailored grocery box delivery," which sends boxes of healthy groceries to families based on their specific health needs.

The study aims to answer:

  1. Can this grocery delivery program improve families' access to healthy foods and support better eating habits?
  2. Will families use the groceries provided, and how effective is the program overall?

To answer these questions, researchers will:

  • Work with the community to design the grocery program and make sure the foods meet families' cultural preferences.
  • Test how well the program can be carried out in real-world settings.
  • Compare how the program affects families' access to healthy food, eating habits, and use of the grocery boxes.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The overarching goal of this project is to address nutrition insecurity among diverse low-income households with children by designing and piloting an intervention strategy grounded in Food Is Medicine (FIM). Leveraging existing online grocery technology, this project seeks to enhance nutrition security through a "medically tailored grocery box delivery" program. We aim to: 1) conduct formative research with a community engagement process to inform the intervention design and ensure foods are culturally acceptable and appropriate; 2) apply implementation strategies to assess the extent to which the intervention can be implemented in the intended setting exactly as evaluated; 3) compare preliminary efficacy of the program on nutrition security, dietary intake, and redemption rate.

Target Population: The study will be conducted in low-income, diverse neighborhoods of New York City, specifically in the South Bronx. Selection of the community was based on the highest poverty levels, chronic disease prevalence, and ethnic diversity. The target population includes households with young children (< age 10) at risk for food insecurity, primarily English or Spanish speakers, participating in SNAP or meeting income criteria < 130% FPL), and access to online ordering through a smartphone or computer.

Approach: Recruitment will be conducted at Bronx Health REACH, a community-based organization located in the South Bronx that serves residents of low-income and SNAP-eligible participants. SNAP-Ed provider and researchers will build the grocery box using Instacart. We will interview the provider to elicit barriers and opportunities for improvement and scalability of the program in other community settings. The formative research plan for the pilot study includes the incorporation of two focus groups at the beginning and end of the intervention, each comprising 10-12 participants. The pilot study will partner with Instacart, utilizing Instacart Care Carts for the "medically tailored grocery delivery" in which researchers order and deliver groceries on behalf of participants. Although families are not able to modify the order, they select when and where they want the grocery box delivered.

A total of 30 households will be selected for the program and will receive the grocery box for 12 weeks. Participants will receive groceries that contain fresh, frozen, or canned fruits, vegetables, legumes, whole grains, and low-sugar low-fat snacks. Evaluation of the intervention will encompass a comprehensive assessment of household nutrition security and dietary intake among children and caregivers. Pre- and post-assessments will evaluate household nutrition security, and diet intake among children and their caregivers using 24-hour recalls and veggie meter assessments. Additionally, SNAP-ED providers will be interviewed to gather insights into their experiences with program delivery and the utilization of Instacart for grocery box orders. A benchmark (i.e., minimum acceptable values) will be set a priori for feasibility (i.e., recruitment, randomization, intervention fidelity, and retention rates) and acceptability following the RE-AIM framework. Instacart data will track orders, deliveries, and confirmations to assess redemption rates. Acceptability will be assessed as participant satisfaction with the intervention materials. To evaluate preliminary efficacy, linear mixed-effects models with random effects to account for repeated caregiver measures will be used.

Study Type

Interventional

Enrollment (Actual)

27

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New York
      • New York, New York, United States, 10035
        • Bronx Health REACH

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Reside in low-income neighborhoods of the South Bronx, New York City.
  • Have children under the age of 10 in the household.
  • Primarily English or Spanish speakers.
  • Participating in the Supplemental Nutrition Assistance Program (SNAP) or meeting income criteria (< 130% of the Federal Poverty Level).
  • Have access to online ordering through a smartphone or computer.

Exclusion Criteria:

  • Households residing outside the designated low-income neighborhoods of the South Bronx.
  • No children under the age of 10 in the household.
  • Unable to communicate in English or Spanish.
  • Not participating in SNAP or not meeting income criteria.
  • Lack access to online ordering through a smartphone or computer.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: FoodBox
Participants will receive a grocery box for 12 weeks. Participants will receive groceries that contain fresh, frozen, or canned fruits, vegetables, legumes, whole grains, and low-sugar low-fat snacks.
  • Time Needed: 12 weeks (duration of intervention)
  • Description: Participants will receive grocery boxes containing a selection of food items tailored to their cultural and nutritional needs. They will be asked to utilize the groceries provided and provide feedback on the quality and quantity of items received. The pilot study will partner with Instacart, utilizing Instacart Care Carts for the "medically tailored grocery delivery" in which researchers order and deliver groceries on behalf of participants. Although families are not able to modify the order, they select when and where they want the grocery box delivered.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of the FOODBOX pilot
Time Frame: 12 weeks

Grocery Box Delivery and Usage: Participants will receive grocery boxes containing a selection of fresh, frozen, or canned fruits, vegetables, legumes, whole grains, and low- sugar, low-fat snacks. Information regarding the receipt and utilization of grocery boxes will be collected, including delivery confirmation, redemption rates, and feedback on the quality and quantity of food items received.

Participant Feedback and Satisfaction: Participants will have opportunities to provide feedback on the intervention materials, delivery process, and overall satisfaction with the program. This feedback may be collected through surveys, interviews, or focus groups conducted at various points during the intervention period.

12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Food Security
Time Frame: 12 weeks
We will use the 18-item USDA Household Food Security Module to assess food security of families. This is a three-stage design with screeners. Screening keeps respondent burden to the minimum needed to get reliable data. Most households in a general population survey are asked only three questions (five if there are children in the household).
12 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fruit and Vegetable Intake
Time Frame: 12 weeks
Participants will undergo dietary intake assessments to evaluate their consumption of fruits and vegetables. In addition, participants will be assessed using a Veggiemeter by the research team, a device designed to measure vegetable intake.
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Angela Trude, PhD, New York University
  • Principal Investigator: Roger Figueroa Baotista, PhD, Cornell University

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 Major Dates

Study Start (Actual)

May 13, 2025

Primary Completion (Actual)

September 30, 2025

Study Completion (Actual)

September 30, 2025

Study Registration Dates

First Submitted

January 17, 2025

First Submitted That Met QC Criteria

March 10, 2025

First Posted (Actual)

March 11, 2025

Study Record Updates

Last Update Posted (Actual)

February 3, 2026

Last Update Submitted That Met QC Criteria

January 30, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • IRB0010546

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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