πŸ›οΈ Verified NIH Record β€’ Updated 2024-12-06

Using Wearable Sensors To Understand Low Blood Sugar in Type 1 Diabetes (NCT06727071)

Assessment of Impaired Counterregulatory Hormones and Cardiovascular Risk Using Modern Wearable Sensors in People Living With Type 1 Diabetes.

🟑 Not Yet Recruiting Observational / Diagnostic 🩺 Clinical Procedure Protocol Sponsor: University of California, San Diego

🩺 Plain-English Summary (8th-Grade Level)

This is a single-site study using wearable sensor technology (CGM and smartwatch) to better explain low blood sugars in patients living with type 1 diabetes. Up to 20 participants with T1D will wear a continuous glucose monitor (CGM) and a smartwatch to collect information about hypoglycemia (low blood sugar), heart rate variability (HRV), and sleep for 4 weeks. The main goal is to create a hypoglycemia risk score using wearable sensor metrics that can be easily applied to all patients with T1D to identify those at greater risk of hypoglycemia.

Who can join: Review the eligibility criteria below.

Location: University of California, San Diego - ACTRI β€” La Jolla, California

Age range: 18 Years to 75 Years

πŸ§ͺ Interventions in This Study

  • Hyperglycemic clamp (PROCEDURE)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • University of California, San Diego - ACTRI β€” La Jolla, California

πŸ“ž Contact the Study Coordinator

Phone: (858) 246-2169

Email: t1dresearch@health.ucsd.edu

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

πŸ’° 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 Β§ 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.

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—