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Adds glucose monitors to text message diabetes education for type 2 diabetes

Tests text message diabetes education with continuous glucose monitors in adults with type 2 diabetes.

Key facts

Who runs it
Scripps Whittier Diabetes Institute
Where
San Diego, United StatesSee the site
Trial code
Registry title
Enhancing Digitally Delivered Diabetes Education With Real-Time CGM
Status
Recruiting
People taking part
140 people, planned
Started
3 Apr 2025
Expected to end
30 Apr 2027
Type of study
Interventional, 2 groups
Treatments tested
  • Dulce Digital Text Messaging Intervention
  • CGM Device
Record updated
6 March 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with type 2 diabetes who do not use insulin or a CGM. They get diabetes text messages, and some also wear a CGM for 6 months.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Type 2 diabetes with an A1c between 7.5% (58 mmol/mol) and 12.0% (108 mmol/mol) in the last 90 days.
Earlier treatment
Must not be using insulin therapies. Must not be using a CGM now.
Biomarker or test result
A1c between 7.5% (58 mmol/mol) and 12.0% (108 mmol/mol) in the last 90 days.

Main reasons for not taking part

  • Using insulin therapies
  • Pregnant
  • Currently using a CGM
  • Taking part in another diabetes-related study

The registry criteria, word for word

Show all 10 criteriaShow less

Who can take part

  • Diagnosed with type 2 diabetes
  • Are not currently using a CGM
  • Are not using insulin therapies
  • Speak English, Spanish or Arabic
  • Have A1c between 7.5% and 12.0% in last 90 days
  • Have a cellphone that can receive/send text messages and counts steps

Who cannot take part

  • Are using insulin therapies
  • Are currently using a CGM
  • Are currently participating in another diabetes-related study
  • Are pregnant

Where in United States

  • Scripps Whittier Diabetes InstituteSan Diego, United StatesContact: Athena Philis-Tsimikas, MDTaking people

About the trial

What the trial wants to find out

The current research study will add continuous glucose monitoring devices to the evidence-based text messaging diabetes education program for patients with type 2 diabetes for 6 months. Results on the effectiveness of this intervention will be compared for non-insulin using patients.

The 2 groups in the trial

  • CGM GroupTreatment being tested

    Participants will be provided continuous glucose monitors (Dexcom G7) to monitor blood glucose for the entire duration of this study (i.e., one new device every 10 days for a total of 18 devices to last up to 6 months).

    Treatment: Dulce Digital Text Messaging Intervention and CGM Device

  • Usual Care Blood Glucose Monitoring GroupOther group

    Participants will use standard blood glucose monitoring devices that are covered by health insurance.

    Treatment: Dulce Digital Text Messaging Intervention

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Enhancing Digitally Delivered Diabetes Education With Real-Time CGM: A Comparative Study in People With Type 2 Diabetes
Plain-language title
Adds glucose monitors to text message diabetes education for type 2 diabetesGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
6 March 2026