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Enhancing Digitally Delivered Diabetes Education With Real-Time CGM

Enhancing Digitally Delivered Diabetes Education With Real-Time CGM: A Comparative Study in People With Type 2 Diabetes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06296550
Enrollment
140
Registered
2024-03-06
Start date
2025-04-03
Completion date
2027-04-30
Last updated
2026-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Type 2

Keywords

Diabetes, CGM, Diabetes Education

Brief summary

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.

Detailed description

The current research study seeks to investigate the impact of incorporating Continuous Glucose Monitoring (CGM) into the evidence-based text messaging diabetes education program, Dulce Digital, focusing on individuals with Type 2 Diabetes (T2D) who are not on insulin therapy. This innovative approach stems from the rationale that real-time continuous glucose monitoring (CGM) can offer valuable insights into glycemic control, thereby enhancing diabetes self-management. In standard care, individuals with T2D, particularly those not on insulin, may not routinely have access to CGM devices. The CGM device, an integral part of recommended diabetes therapy, is FDA approved for use in all people with diabetes. However, reimbursement for CGM devices varies by health plans, and currently, Centers for Medicare & Medicaid Services (CMS) does not reimburse for their use in non-insulin-using diabetes, except in cases of repeated severe hypoglycemia. Despite this, the investigators hypothesize that there are both clinical and financial benefits to providing a CGM device during diabetes self-management education for individuals with non-insulin-using T2D. This study aims to determine if adding a CGM device for this patient category yields significant benefits, contributing to the understanding of the potential advantages and informing future diabetes care practices.

Interventions

OTHERDulce Digital Text Messaging Intervention

Text-based education support program: * Participants will receive text messages about diabetes and how to take care of diabetes and health. Participants will receive 2-3 messages every day for first 3 months, and then will slowly decrease over the last 3-months. * Participants will also receive text messages that will ask them to test their blood sugar and text back blood sugar reading.

Participants will be provided continuous glucose monitors (Dexcom G7) to actively 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). In addition, participants will attend an information session (group or individual; in-person or virtual) that will provide instructions on using continuous glucose monitors.

Sponsors

Scripps Whittier Diabetes Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
HbA1c6 monthsMeasures participants A1c using lab results provided from healthcare provider.

Secondary

MeasureTime frameDescription
CGM Metric Time in Range6 monthsMeasures the percentage of time a participant's blood glucose levels stay within the target range using CGM device.
CGM Metric Time above Range6 monthsMeasures the percentage of time a participant's blood glucose levels exceed the target range using CGM device.
CGM Metric Time Below Range6 monthsMeasures the percentage of time a participant's blood glucose levels fall below the target range using CGM device.
Summary of Diabetes Self Care Activities (SDSCA) Survey6 monthsSummary of Diabetes Self Care Activities Survey measures frequency and consistency of diabetes self-care activities during the past 7 days. Possible scores range from 0 (0 Days to 7 (7 Days). Higher scores indicate better compliance with diabetes self-care.
Diabetes Distress Scale6 monthsThe Diabetes Distress Scale measures four critical dimensions of diabetes distress for participants: emotional, burden, regimen distress, interpersonal distress and physical distress. Possible scores range from 1 (Not a Problem) to 6 (A Very Serious Problem) with higher scores indicating higher levels of diabetes-related distress.

Countries

United States

Contacts

CONTACTKallie Brown, PhD
brown.kallie@scrippshealth.org858-258-3555
CONTACTAthena Philis-Tsimikas, MD
philis-Tsimikas.athena@scrippshealth.org877-944-8843
PRINCIPAL_INVESTIGATORAthena Philis-Tsimikas, MD

Scripps Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026