Actively Recruiting

Phase Not Applicable
Age: 7Years - 12Years
All Genders
Healthy Volunteers
ID06861868

Early Brain Development and Child Nutrition and Obesity Study on Childhood Obesity Risk

Led by Johns Hopkins University · Updated on 2026-05-07

210

Participants Needed

4

Research Sites

N/A

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

N

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating why some children develop obesity by studying eating behaviors, genetic and environmental factors, and brain development. This project, RESONATE, extends a larger study called RESONANCE and focuses on children aged 7 to 12 years. The goal is to understand how early brain development and appetite-related behaviors contribute to obesity risk during middle childhood, a critical time for long-term metabolic health. The study involves a single group of participants who undergo various assessments including meal tests, behavioral tasks, and functional MRI scans. These tests measure food intake, responses to food-related cues, cognitive control, and brain activity related to appetite. Data collected will also include measures of weight and body fat to examine how brain function and behavior relate to obesity development. Participants will take part in tests such as eating from a buffet meal, snack intake when not hungry, and MRI tasks that observe brain responses to food and control stimuli. Researchers will track calorie consumption, body mass index, reward responses, and cognitive control during these activities. The study aims to link these findings with early-life risk factors to better understand obesity mechanisms, supporting the future creation of targeted preventive interventions.

CONDITIONS

Brief Title

Brain and Behavior Influences on Obesity Development From Infancy Through Childhood

Who Can Participate

Age: 7Years - 12Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be from the RESONANCE cohort
  • Participants must be between 7 and 12 years old during the study period
  • Participants must have no food allergies
Not Eligible

You will not qualify if you...

  • In utero exposure to alcohol, cigarettes, or illicit substances
  • First trimester fetal ultrasound abnormalities
  • Complicated pregnancy, such as pre-eclampsia
  • Complicated delivery including APGAR scores less than 8 or neonatal intensive care unit admission
  • History of neurological disorders like epilepsy
  • History of psychiatric disorders such as anxiety or depression requiring medication
  • History of developmental disorders including autism spectrum disorder or dyslexia
  • Contraindications for MRI such as metal in the body or claustrophobia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo tests including fMRI tasks and meal tests to assess brain function, eating behavior, and weight.

1 visit (in-person)

Long-term Monitoring

Duration - Up to several years until study completion

Participants' brain development, appetitive behaviors, and obesity risk factors are observed over time to understand their impact on obesity development.

Follow-up visits timing may vary depending on study schedule

Trial Site Locations

Total: 4 locations

1

Hugo W. Moser Research Institute at Kennedy Krieger, Inc.

Baltimore, Maryland, United States, 21205

Active, Not Recruiting

2

Johns Hopkins University School of Medicine

Baltimore, Maryland, United States, 21287

Active, Not Recruiting

3

Rhode Island Hospital

Providence, Rhode Island, United States, 02903

Actively Recruiting

4

University of Washington

Seattle, Washington, United States, 98109

Active, Not Recruiting

Loading map...

Research Team

S

Susan Carnell, PhD

V

Viren D'Sa, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

Similar Trials

Nutritional Approach for the Transformation and Reduction of...

Metabolic Syndrome

Actively Recruiting

1 location

A Double-Blind, Randomized Placebo-Controlled Study to Evalu...

Obesity and Overweight

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here