MedTrace Logo

Disordered Eating Risk in Pediatric Obesity Treatment Using a Digi-Physical Tool

NCT06807489 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 312

Last updated 2026-04-30

No results posted yet for this study

Summary

The goal of this observational study is to evaluate the risk of developing disordered eating behavior or an eating disorder among children and adolescents with obesity who have used a digi-physical treatment tool with daily measurements conducted at home.

The primary outcomes are to:

* Evaluate the proportion of patients exhibiting documented signs of disordered eating behaviors during or after treatment (e.g., caloric restriction, skipping meals, binge eating).
* Evaluate the proportion of patients diagnosed with an eating disorder (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder) during or after treatment.

Patients at Martina Childrens Hospital, Stockholm, Sweden, who have been treated with the digi-physical treatment tool will be included and their patient records will be reviewed for eating disorder diagnosis or a disturbed eating behavior.

Conditions

  • Childhood Obesity
  • Disordered Eating
  • Binge Eating Disorder
  • Anorexia Nervosa
  • Bulimia Nervosa

Interventions

DEVICE

Digi-physical treatment tool

A digital treatment tool named Evira will be used to provide the treatment.

Sponsors & Collaborators

Principal Investigators

  • Pernilla Danielsson Liljeqvist, Associate Professor · Karolinska Institutet

Eligibility

Min Age
6 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-01
Primary Completion
2025-05-08
Completion
2025-12-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06807489 on ClinicalTrials.gov