A hospital handout may do more than discharge — it could fight hunger at home
NCT ID NCT04171999
First seen Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time
Summary
This trial tests whether giving caregivers of hospitalized children a personalized list of community resources — covering food, housing, transportation, and more — along with a brief explanation, can improve their confidence in finding help and their satisfaction with hospital discharge. About 660 English- or Spanish-speaking caregivers from 27 Chicago-area zip codes will take part. The goal is to see if this simple, low-cost intervention can ease the burden of food insecurity and related social needs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a tailored list of community resources for food insecurity and other health-related social needs, delivered with a brief educational script
- What this could lead to
- If effective, this low-cost intervention could become a standard part of hospital discharge planning, helping families better manage food insecurity and related needs.
- What could go wrong
- The trial is relatively small and tests a behavioral intervention, so results may not generalize to all hospitals or regions. Caregiver self-reports may not reflect actual resource use or long-term food security.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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660 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Sep 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Native English or Spanish speaker * Living in 1 of 27 zip codes in the study's target region * Self-identify as a primary caregiver of a child \<18 years old hospitalized in a large urban children's hospital * Ability to send and receive text messages * Access to a mobile phone and agrees to receive text messages from the study Exclusion Criteria: * Previous participation in a CRx research study. * Caregivers of newborns in the hospital * Patient hospital stay is less than 24 hours * Patient hospital stay is 30 days or more * Patient has an eating disorder as indicated in the EMR
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Chicago
Chicago, Illinois, 60637, United States
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Other studies related to the condition(s) this trial covers.
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