New program aims to keep kids with feeding tubes out of the ER
NCT ID NCT07383272
First seen Jun 25, 2026 · Last updated Sep 03, 2026 · Updated 4 times
Summary
This study tests a new education program for parents of children who just got a feeding tube (like a G-tube or NG-tube). The program teaches parents how to care for the tube, get supplies, and handle problems. Researchers want to see if this helps parents feel more confident and reduces unplanned trips to the ER or clinic. The study will compare families who get the extra education to those who receive usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- education program on feeding tube care
- What this could lead to
- If successful, this could lead to a standard discharge protocol that helps parents feel more prepared and reduces emergency visits for children with feeding tubes.
- What could go wrong
- This is a small, early-stage study with only 20 participants, so results may not apply to all hospitals or families. The education program may not significantly change outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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May 2028
An estimate. End dates often move.
- 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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Up to 17 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Patients must be within the age range of 0 to 17 years. * Patients who have recently had an enteral feeding tube placed (G-tube, J-tube, GJ-tube, or NG-tube). * The patient must be hospitalized at the time of the study and scheduled for discharge within the study period (before discharge). * A legal guardian must be available to participate in the study, complete questionnaires, and engage in the educational sessions. * Both the pediatric patient and their caregiver must be willing to participate in the study, including completing surveys and receiving educational materials. Exclusion Criteria: * Patients who have had an enteral tube (G-tube, J-tube, GJ-tube, or NG-tube) for more than a short period (e.g., those who have had tubes in place for more than 3 months) may be excluded, as the study is focused on newly placed feeding tubes. * Patients aged 18 years or older are excluded from the study, as the project targets pediatric patients specifically. * If the caregiver (or the child, where applicable) has significant cognitive or language barriers that would prevent them from understanding the educational content or completing the surveys, they may be excluded. * Families who do not speak English may be excluded. * Patients with significant comorbidities or unstable clinical conditions that would make participation in the discharge education protocol impractical will be excluded. This includes, but is not limited to, patients with severe respiratory failure requiring nitric oxide therapy, hemodynamic instability requiring blood pressure medications (e.g., vasopressors), or other acute medical conditions requiring active intensive care. Patients who are stable and preparing for discharge, even after a prolonged NICU or PICU stay, will not be excluded. * Only legal guardian can enroll child. * Patients whose caregivers are unable or unwilling to adhere to study protocols (e.g., participating in follow-up assessments or completing questionnaires) may be excluded to ensure consistency and reliable data collection.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Illinois at Chicago (UI Health)
Chicago, Illinois, 60612, United States
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