Feasibility of a Diabetes Self-Management Program With Continuous Glucose Monitoring for Adults With Type 2 Diabetes
Starting soon · Not applicable
Conditions studied: Type 2 Diabetes
In brief
The purpose of this study is to determine if combining a virtual diabetes self-management program (DECIDE®) with continuous glucose monitoring (CGM) is practical and well-received by adults with type 2 diabetes. Twenty participants will attend the 9-week, virtual DECIDE Self-Management Program. They will receive CGM sensors to wear during the 22-week study to track their blood sugar. Participants will complete questionnaires at three time points -- at baseline, 1 week after the DECIDE Program ends, and 3 months after the DECIDE Program ends. They will also complete a blood draw to measure hemoglobin A1C at baseline and 3 months after the intervention ends. Additionally, they will complete a brief interview after the program ends to gather insights into participants' experiences with the program. The study aims to examine whether this integrated approach will be both feasible and acceptable, potentially leading to better diabetes management and improved health outcomes.
Key facts
- Study ID
- NCT07743307
- Run by
- Northwell Health
- People needed
- 20
- Starts
- 2026-08-01
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-08-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Aged 18 years or older
- Diagnosis of type 2 diabetes
- Suboptimal hemoglobin A1C (8.0% or greater) based on a laboratory result in the past 3 months
- Access to and capability of using a smart cellular device
- Smart cellular device compatible with the Freestyle Libre CGM smartphone application
- Capable of giving informed consent
You may not qualify if…
- Currently using CGM
- Non-English speaking
- Unavailable to attend the virtual DECIDE group
- Unavailable for follow-up
- Currently pregnant
- Currently on dialysis
Where it is running
- Northwell Heath — Manhasset, New York, United States
Full record on ClinicalTrials.gov
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