Pediatric Feeding Disorder Evolution in Amiens University Hospital (EVOLTOA)

April 8, 2025 updated by: Centre Hospitalier Universitaire, Amiens
Pediatric feeding disorders (PFDss) affect children with age-inappropriate oral intakes lasting at least 2 weeks, associated with medical, nutritional, psychosocial or feeding skills dysfunction. Feeding is a complex function involving the digestive tract, and different structures. It evolves throughout the child's development. It involves the caregiver-child relationship. Dysfunction of one or more of these systems may be the cause of pediatric feeding disorders. PFDs affect 25% of children, 5% with severe forms. PFDs can have severe nutritional consequences. They often cause malnutrition, even undernutrition, and sometimes overweight.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

33

Contacts and Locations

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

Study Contact

Study Locations

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Children <18 years old with at least two pediatric gastroenterology PFDs consultations at CHUAP , with an inapropriate oral intakes for at least 2 weeks, Association with medical, nutritional, psychosocial or eating-skills dysfunction.

Description

Inclusion Criteria:

  • Children <18 years old
  • with at least two pediatric gastroenterology PFDs consultations at CHUAP ,
  • with an inapropriate oral intakes for at least 2 weeks,
  • Association with medical, nutritional, psychosocial or eating-skills dysfunction.

Exclusion Criteria:

  • anorexia nervosa

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 6 months
Frequency of children with Pediatric feeding disorders disappearance
6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 1 year
1 year
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 2 years
2 years
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 3 years
3 years
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 5 years
5 years
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 8 years
8 years
Frequency of children with Pediatric feeding disorders disappearance
Time Frame: 10 years
10 years

Collaborators and Investigators

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

Sponsor

Centre Hospitalier Universitaire, Amiens

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)

March 1, 2025

Primary Completion (Estimated)

May 1, 2025

Study Completion (Estimated)

May 1, 2025

Study Registration Dates

First Submitted

April 8, 2025

First Submitted That Met QC Criteria

April 8, 2025

First Posted (Actual)

April 15, 2025

Study Record Updates

Last Update Posted (Actual)

April 15, 2025

Last Update Submitted That Met QC Criteria

April 8, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PI2025_843_0019

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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