Obesity Trial, Recruiting NCT06861868 Sponsor: Johns Hopkins University Condition: Obesity
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Obesity Trial, Recruiting

NCT06861868
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are already part of the RESONANCE research cohort (an existing group of study participants) and who will be between 7 and 12 years old during the study period
  • People in that group who have no food allergies

Who may not be able to join:

  • People who were exposed to alcohol, cigarettes, or illegal substances before birth (while in the womb)
  • People who had abnormalities detected on an ultrasound scan during the first three months of pregnancy
  • People whose mother had a complicated pregnancy, such as pre-eclampsia (a condition involving high blood pressure during pregnancy)
  • People who had a difficult birth, including a low APGAR score (a measure of a newborn's health at birth) below 8, or who needed care in a neonatal intensive care unit (NICU) after birth
  • People with a history of neurological conditions (such as epilepsy), mental health conditions that required medication (such as anxiety or depression), or developmental conditions (such as autism spectrum disorder or dyslexia)
  • People who are unable to have an MRI scan, for example due to metal in the body or fear of enclosed spaces (claustrophobia)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Susan Carnell, PhD, Johns Hopkins University

Phone: 410-955-7192

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
2 December 2024
Est. completion
31 March 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Meal test intake as assessed by total kilocalories consumed; Weight/adiposity as assessed by BMI; Food-related reward as assessed by food-related delay discounting task; Food-related cognitive control as assessed by food-related go/no-go task; Functioning in brain appetite circuits as assessed by cue reactivity task; Functioning in brain appetite circuits as assessed by cognitive control task

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov