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NCT06638099 · ClinicalTrials.gov registry record · NA

Increasing CGM Use Among Patients With T2D

A NA study of Diabetes Mellitus, Type 2 and Diabetes, sponsored by San Diego State University.

Recruiting
Registry status
NA
Development phase
318
Enrollment target
2
Study locations

NCT06638099: Recruiting NA study of Diabetes Mellitus, Type 2 and Diabetes, sponsored by San Diego State University.

NCT06638099 is a NA study of Diabetes Mellitus, Type 2 and Diabetes that is actively recruiting participants, run by San Diego State University. The registered enrollment target is 318 participants, below the 4,484-participant average among 348 other Diabetes Mellitus, Type 2 trials with a reported enrollment target (93% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06638099, a NA study of Diabetes Mellitus, Type 2 and Diabetes, is actively recruiting participants, sponsored by San Diego State University.

RECRUITING
Registry status
NA
Development phase
318 participants
Enrollment target
2
Study locations

Study Summary

Study Overview: This interventional study aims to assess whether training healthcare professionals (HCPs) increases the number of continuous glucose monitor (CGM) prescriptions for patients with Type 2 Diabetes in a Federally Qualified Health Center serving a predominantly Hispanic/Latino population. Research Questions: Does HCP training enhance CGM prescription rates in a primary care setting? Does receiving a CGM prescription lead to improved Type 2 Diabetes control, as measured by Hemoglobin A1c levels? What barriers do patients face when prescribed and using CGMs? Given the significant impact of CGMs on diabetes management, this project seeks to improve CGM utilization among eligible patients through a focused intervention for HCPs and evaluate diabetes outcomes for those who do and do not receive a CGM. Methodology: HCPs and staff from three clinics within the same healthcare system will undergo a brief, in-person training on current clinical guidelines and insurance eligibility for CGMs. A booster session will follow about one month later to reinforce learning and address any prescribing challenges. Training efficacy will be evaluated by comparing CGM prescription rates before and after training using electronic health records. HCPs will complete pre- and post-training surveys to assess changes in knowledge, beliefs, and prescribing practices related to CGMs. Additionally, a small subset of prescribers will participate in interviews about their experiences with CGM prescriptions four months post-training. Patient Recruitment and Surveys: Patients with Type 2 Diabetes will be recruited for surveys at baseline, and at 3 and 6 months. These surveys will gather information on their diabetes management experience, levels of diabetes distress, and whether CGM discussions occurred with their primary care provider. Participants who received CGM prescriptions will share their experiences and any barriers encountered. A subset will also be invited for interviews

Primary Outcome

Determine if the proportion of patients with T2D who are prescribed CGM increases following the intervention as compared to pre-intervention data

Interventions

  • BEHAVIORAL CGM Toolkit Prescriber Training

Study Locations (2)

California

  • Innercare Inc - El Centro
  • Innercare, Inc - El Centro

Trial Details

FieldValue
Enrollment Target 318 participants
Start Date 2024-11-04
Est. Completion 2026-06-30
Phase NA
San Diego State University

118 total trials

What NCT06638099 shows while recruiting

NCT06638099 is an interventional study that assigns participants to a tested intervention. The registered 318 participants enrollment target is mid-sized for trials with a published cap, below the 4,484-participant average among 348 other Diabetes Mellitus, Type 2 trials with a reported enrollment target (93% lower).

The record links to 4 conditions, with Diabetes Mellitus, Type 2 appearing as the primary indexed condition, and to 1 intervention - of which CGM Toolkit Prescriber Training is the first listed.

NCT06638099 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06638099 about?

NCT06638099 is a clinical study titled "Increasing CGM Use Among Patients With T2D". Study Overview: This interventional study aims to assess whether training healthcare professionals (HCPs) increases the number of continuous glucose monitor (CGM) prescriptions for patients with Type 2 Diabetes in a Federally Qualified Health Center serving a predominantly Hispanic/Latino populatio...

What is the current status of trial NCT06638099?

This trial is currently recruiting. It is a NA study. The enrollment target is 318 participants. The study started on 2024-11-04. Estimated completion is 2026-06-30.

What conditions does trial NCT06638099 study?

This clinical trial studies the following conditions: Diabetes Mellitus, Type 2, Diabetes, Diabetes Mellitus, Diabetes Mellitus Type 2 (T2DM).

What interventions are being tested in trial NCT06638099?

The interventions under investigation include: CGM Toolkit Prescriber Training (BEHAVIORAL).

Who is sponsoring clinical trial NCT06638099?

This trial is sponsored by San Diego State University, which has 118 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06638099 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Diabetes Mellitus, Type 2

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06638099's enrollment target sits among peer trials

318 117th of 348 higher than 232 of 348 other Diabetes Mellitus, Type 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Diabetes Mellitus, Type 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT06638099, the US trial registry maintained by the National Library of Medicine. NCT06638099 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.