Stanford Pediatric Healthy Weight Index for Obesity & Overweight

This study is developing a simple way to measure how well the body uses insulin and overall heart and metabolic health in children and teenagers with obesity. It uses a Remote Monitoring Program where participants wear continuous glucose monitors and fitness trackers. Researchers will collect data from these devices, along with lab tests, to understand how activity and glucose levels relate to metabolic problems. You may be able to join if you are 10 to 18 years old, have Class 2 or 3 obesity, and are already in the Adolescent Bariatric Program at Stanford Children's, eligible for either bariatric surgery or GLP1 Receptor Agonist Therapy. The study aims to see how much body mass index (BMI), body weight, and fasting glucose levels change over about 4 months. The current recruitment status is unclear.

Study design
This is an interventional study with a planned enrollment of 120 participants. It is a prospective cohort study, meaning participants are followed over time.
What's involved
You would wear a continuous glucose monitor and a wearable fitness device for the duration of the study. Monitoring will occur at three time points: before treatment, during early treatment, and 3 months after treatment or dose stabilization.
Compensation
Not stated in the trial record.
Follow-up
Primary endpoints are measured from baseline through study completion, which is an average of 4 months.

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NCT07316816

Stanford Pediatric Healthy Weight Index

Recruiting
NAAges 10–18InterventionalDiagnostic
Stanford University
~120 participants
Updated 2026-01-05 on ClinicalTrials.gov
What's tested:Remote Monitoring Program

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent Reduction in BMI
Measured over baseline through study completion, an average of 4 months
+6 more outcomes measured
Obesity & Overweight
1 sites across 1 states
California1

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Eligibility criteria

Inclusion

Class 2 and 3 obesity
Patient in the Adolescent Bariatric Program at Stanford Children's that is eligible for either laparoscopic sleeve gastrectomy or GLP1 Receptor Agonist Therapy
Willingness to wear a CGM and physiological monitor for the duration of the study.

Exclusion

Hypothalamic and syndromic obesity
BMI \> 55
Plan to undergo bariatric surgical procedure other than sleeve gastrectomy
Prior bariatric surgical procedure
Active GLP treatment (within past 3 months)
Unable to read, understand, or complete the informed consent in English or Spanish
  • Percent Reduction in BMIbaseline through study completion, an average of 4 months

    assessment of change in BMI from pre-intervention to post-intervention

  • Body Weightbaseline through study completion, an average of 4 months

    Change in body weight (kg)

  • Fasting Glucosebaseline through study completion, an average of 4 months

    change in fasting glucose levels from pre-intervention to post-intervention

  • Fasting Insulinbaseline through study completion, an average of 4 months

    change in fasting insulin levels from pre-intervention to post-intervention

  • HbA1cbaseline through study completion, an average of 4 months

    change in HbA1c levels from pre-intervention to post-intervention

  • Lipid Panelbaseline through study completion, an average of 4 months

    changes in lipid panel levels from pre-intervention to post-intervention

  • Liver Enzymesbaseline through study completion, an average of 4 months

    changes in liver enzymes from pre-intervention to post-intervention