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NCT06082830Completed

Helping Educate and Advance Learning Through Healthy Bite-Sized Eating Strategies

Digital Intervention to Improve Diet Quality in Adolescents With Overweight or Obesity

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

The goal of this clinical trial is to compare the effectiveness of a mobile health intervention in adolescents (14-17 years) with overweight or obesity. The main question\[s\] it aims to answer are: 1) is a digital-based diet quality intervention for adolescents with overweight or obesity feasible and 2) is there preliminary effectiveness in improving diet quality? Participants will: 1. Complete three-day 24-hour dietary recalls 2. Collect urine samples 3. Wear a continuous glucose monitor, sleep tracker, and physical activity tracker Researchers will compare control and intervention groups to see if diet quality and meal timing traits improve as assessed by 24-hour dietary recalls, a novel urine biomarker, and continuous glucose monitoring (CGM).

Status (registry)
Completed
Study type
Interventional
Enrollment
15 (actual)
First submitted
9 Oct 2023
Start date
1 Oct 2024
Primary completion date
14 Jun 2025
Lead sponsor
Children's Hospital of Philadelphia
Diseases
Obesity
NCT number
NCT06082830

What you commit to

  • Study type: Interventional
  • Participants enrolled: 15
  • From 1 Oct 2024 to the primary completion date, 14 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Regularly taking medications that may result in weight loss, appetite stimulation or suppression, and/or fluctuations in fluid status.

Other illness

  • History of an eating disorder diagnosis (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder, avoidant restrictive food intake disorder).
  • History of a condition that may alter dietary intake (e.g., diabetes, Celiac's disease, phenylketonuria, cystic fibrosis).

Other

  • Currently being followed by a registered dietitian.
  • Pregnant or lactating females.
  • Have a parent, guardian, or family member that works for the Division of Gastroenterology, Hepatology, and Nutrition at CHOP.

Who the study is looking for

  • Aged 14-17 years old.
  • At risk for diet quality that is poor or needs improvement (HEI score \< 80) determined by participants baseline 24-hour diet recall data.
  • Body mass index between the 85th and 99th percentile for age and sex on at least two occasions at least six months apart in the medical record in the last five years.
  • Have access to a phone capable of receiving text messages.

Age in the registry: 14 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Children's Hospital of Philadelphia
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.