Clinical Decision Support With Continuous Glucose Monitoring Data for Managing Type 2 Diabetes (NCT07394075) | Clinical Trial Compass
By InvitationNot Applicable
Clinical Decision Support With Continuous Glucose Monitoring Data for Managing Type 2 Diabetes
United States150 participantsStarted 2026-03-04
Plain-language summary
The goal of this project is to see if an electronic health record (EHR)-based smart order set with continuous glucose monitoring data to provide decision support can improve blood sugar management in people with type 2 diabetes (T2D) using insulin.
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Type 2 diabetes
* A1c greater than 7.5%
* On insulin therapy
* Use CGM for glycemic monitoring
Exclusion Criteria:
* Pregnancy
* Use of insulin pump or automated insulin delivery system
* Active cancer (other than nonmelanoma skin cancer or low-grade prostate cancer being followed with observation)
* Cognitive barriers requiring assistance of a surrogate or caregiver for insulin management
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial uses continuous glucose monitors and a clinical decision support tool to help manage my Type 2 diabetes — can you explain how that decision support system would actually change the way my care is managed day-to-day compared to what we're doing now?
2Since the main thing being measured is something called the glucose management indicator percentage, what does that number reflect about my blood sugar control, and is it something you're already tracking for me?
3This study is enrolling by invitation only — am I being considered for it, and if so, what made you think it could be a good fit for my situation?
4Because this trial doesn't have a traditional phase number, what does that tell us about how much is already known about this approach's safety and effectiveness, and are there any risks I should be aware of before deciding?
5Would participating in this trial require me to wear a continuous glucose monitor full-time, and how often would I need to come in for appointments or interact with the care team as part of the study?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.