Use of Continuous Glucose Monitors in Children and Adolescents With Obesity (NCT06254768)

🧪 Interventions in This Study

• Continuous glucose monitor (DEVICE)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• Pediatric Endocrinology Division, University of California — Los Angeles, California

📞 Contact the Study Coordinator

Phone: (917) 741-4080

Email: schimatapu@mednet.ucla.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

• 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
• Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
• Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

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• The Family Stress Study - Chronic Stress and Child Adiposity: Testing a Bio-behavioural Model — Guelph, Ontario
• Phentermine/Topiramate in Adolescents With Type 2 Diabetes and Obesity — Minneapolis, Minnesota
• Childhood Obesity Treatment Designed for Low Income and Hispanic Families — Aurora, Colorado
• Growing Healthy Children and Families in Rural Arkansas — Little Rock, Arkansas

Explore by condition: All Pediatric Obesity clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Contact the study coordinator using the phone/email above.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.