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Enrolling by invitationNCT06129877Updated May 7, 2026

CHAMP App Feeding Difficulties Repository

An observational study in Feeding and Eating Disorders of Childhood, Gastrostomy and Feeding Disorder of Infancy and Childhood, sponsored by Children's Mercy Hospital Kansas City. Enrolling by invitation at 1 site in United States. Open to participants aged 1 Month to 18 Years. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Children's Mercy Hospital Kansas City · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
1,000
Ages
1 Month to 18 Years
Sex
All
01

Study summary

This repository will consist of home monitoring data, videos, and images of patients with feeding difficulties for asynchronous remote patient monitoring of manually entered data sent by parents to the healthcare team using the CHAMP App for children with feeding difficulties. This information will be collected under a research protocol and this repository is for future research applications.

Read the detailed description

Around 25% of children are reported to have some degree of feeding issues of whom 3-10% have more severe feeding disorders1. Many of these feeding issues and difficulties can also lead to a need for supplemental nutrition in a child's diet due to the impact on growth. Those requiring supplemental nutrition may find themselves having to be fed using tube feedings (TF), which carries its own set of obstacles and factors to consider. While feeding problems have been estimated to occur in 25%-35% of children observed as exhibiting normal growth, that number may spike to 85% in those with GI-related growth disorders2. This highlights the need to ensure treatment plans and programs are in place to assist this patient population.

At Children's Mercy Hospital, GI specialists care for children who have a variety of conditions, caring for the whole child and addressing physical, mental, emotional, and social aspects. By using a combined approach, and promoting research that seeks to improve care, significant improvements in children's health have been reported. One specialty this has been evident in at Children's Mercy is the cardiac patient population. There have been improvements in growth, feedings, and timeliness of interventions seen with the use of CHAMP® App in the single ventricle population (a statistically significant difference in the frequency of growth failure, with no patients having growth failure during CHAMP use)3-4. By harnessing the experience and knowledge gained through the CHAMP® App research study, there is a great potential for children suffering from GI conditions to also benefit from this form of remote patient management and monitoring, especially when it comes to treating children with supplemental nutrition needs. There are no known Gastroenterology- Feeding mobile health software platforms with a dedicated research repository in pediatrics.

02

Conditions studied

  • Feeding and Eating Disorders of Childhood
  • Gastrostomy
  • Feeding Disorder of Infancy and Childhood

Keywords

  • mHealth
  • Software Platform
  • asynchronous remote monitoring
03

In context

Feeding and Eating Disorders of Childhood

30 studies on the registry are indexed under Feeding and Eating Disorders of Childhood; 3 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 294 across 10 observational studies indexed under Feeding and Eating Disorders of Childhood.

Browse Feeding and Eating Disorders of Childhood studies →

Lead sponsor

Children's Mercy Hospital Kansas City is the lead sponsor of 209 studies on the registry; 22 are open to participants now.

Of its 18 completed or terminated interventional studies of FDA-regulated products, 14 (78%) have results posted.

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

04

Who can participate

Ages eligible
1 Month to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children with feeding difficulties and/or malnutrition

Inclusion criteria

  • Patients enrolling in this research repository must also be enrolled in an applicable study (STUDY00002775, STUDY00003221) wherein they have consented to use CHAMP App
  • Parent-Legally authorized representative can read one of the eleven languages that the CHAMP App is available in.

Exclusion criteria

Exclusion Criteria:

  • All patients and parents/Legally authorized representative not meeting the above specified criteria
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Interventions

  • DeviceCHAMP App

    CHAMP App software platform will have been used in other research studies to be included in the Feeding difficulties repository

06

What researchers measure

Primary outcomes

  1. Feeding difficulty management

    Percent of patients eating all calories by mouth at the end of asynchronous remote monitoring period for feeding management

    Time frame: 12 months

07

Study locations

1 site
  • Children's Mercy Kansas City
    Kansas City, Missouri 64108, 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 May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06129877
Lead sponsor
Children's Mercy Hospital Kansas City
Collaborators
The Gerber Foundation
Responsible party
Lori Erickson (Principal Investigator, Children's Mercy Hospital Kansas City) — Principal investigator
First posted
Nov 13, 2023
Start date
Nov 9, 2023
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
May 7, 2026

Study contacts

Lori Erickson, PhD
principal investigator · Director, Remote Health Solutions Children's Mercy

Oversight

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

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