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CompletedNCT06870526FOODBOXUpdated Feb 3, 2026

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

An interventional study of Food box delivery in Food Insecurity, sponsored by Cornell University. Completed at 1 site in United States. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2026-02-03.

Sponsored by Cornell University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
27
Allocation
Not applicable
Ages
21 Years and older
Sex
All
01

Study summary

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.
Read the 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.

02

Conditions studied

  • Food Insecurity

Keywords

  • Grocery
  • Food delivery
03

In context

Lead sponsor

Cornell University is the lead sponsor of 96 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
27 participants (actual)

Study arms

  • 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.

    Behavioral: Food box delivery

Interventions

  • BehavioralFood box delivery

    * 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.

06

What researchers measure

Primary outcomes

  1. Feasibility of the FOODBOX pilot

    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.

    Time frame: 12 weeks

Secondary outcomes

  1. Food Security

    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).

    Time frame: 12 weeks

Other outcomes

  1. Fruit and Vegetable Intake

    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.

    Time frame: 12 weeks

07

Study locations

1 site
  • Bronx Health REACH
    New York, New York 10035, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06870526
Lead sponsor
Cornell University
Collaborators
New York University
Responsible party
Sponsor
First posted
Mar 11, 2025
Start date
May 13, 2025
Primary completion
Sep 30, 2025
Completion
Sep 30, 2025
Last update
Feb 3, 2026

Study contacts

Angela Trude, PhD
principal investigator · New York University
Roger Figueroa Baotista, PhD
principal investigator · Cornell University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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