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OpenTrials
Active, Not Recruiting

NCT Number: NCT03968055

Remote Monitoring of CGM Data in Pediatric Patients With Newly Diagnosed Type 1 Diabetes (T1D)

To determine if increased targeted contact between patients and the care team can improve diabetes outcomes in the 1st year after diagnosis. We will be using the GluVue platform to remotely view continuous glucose monitor (CGM) data.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

6 month–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Lucile Packard Children's Hospital

Palo Alto, California, 94305, United States

About this study

Based on alerts from GluVue, care team members will proactively reach out to patients and their families for more frequent dose adjustments. We will assess if remote monitoring facilitates contact between the care team and patients and improves glycemic control.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All individuals within one month of T1D diagnosis seen at the Stanford Children's Diabetes Clinic
  • Individuals who plan to receive follow up care at the Stanford Children's Diabetes Clinic
  • Individuals who agree to CGM data integration into the electronic medical record (EMR) for remote monitoring
  • Age: birth to < 21 years of age

Exclusion criteria

  • Diabetes diagnosis other than T1D
  • Diagnosis of diabetes > 1 month prior to initial visit
  • Individuals with the intention of obtaining diabetes care at another clinic
  • Individuals who do not consent to CGM use, CGM data integration, or remote monitoring
  • Individuals > 21 years of age

Treatment and study plan

Integration with Epic

Other

Participants will have CGM data connected to our medical record through an already established pathway (Dexcom app on iOS device to Apple HealthKit to Epic MyChart to Epic)

Other names: GluVue Platform

Primary outcomes

  1. Contacts with the care provider

    Time frame: 1 year

    Prospective chart review to determine the number of contacts between the participant and care team due to remote monitoring

Secondary outcomes

  1. Hemoglobin A1c

    Time frame: 1 year

    Prospective chart review for lab values

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Official study title

The Use of Continuous Glucose Monitor Technology and Remote Monitoring to Change Clinical Outcomes Following New Diagnosis of Type 1 Diabetes in the Pediatric Population

Important dates

Study start
2019
Primary completion
2025
Study completion
2028
First posted
May 30, 2019
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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