Poor glycemic control is the fundamental driver of diabetes-related complications, and while CGM adoption has increased in the management of type 2 diabetes, evidence linking frequency of use to measurable clinical outcomes has remained scant. This large-scale study fills that gap by analyzing real-world data to establish a clear relationship between CGM usage patterns and HbA1C outcomes over 12 months.
This retrospective, propensity score–matched, cross-sectional study used Optum deidentified Market Clarity Data, including insurance claims and electronic medical records collected from January 1, 2019, through December 31, 2023. The dataset included clinical information for 6 months before each participant's index date and 12 months of follow-up.
The study population included 9,258 adults aged 18 years or older with type 2 diabetes and baseline HbA1C levels between 7.0% and 15.0%. The participants were stratified into five groups based on the frequency of CGM use during the 12-month postindex period:
Control group (no CGM use): 4,629 patients
Frequency 1 (≥1 to ≤90 days): 1,081 patients
Frequency 2 (>90 to ≤180 days): 523 patients
Frequency 3 (180 to ≤270 days): 540 patients
Frequency 4 (>270 days): 2,485 patients
Change in HbA1C was analyzed relative to the frequency of CGM use compared to no CGM use by using mixed-model statistical methods.
Results
The mean (SD) age of participants was 55.9 (10.6) years, with 45.4% female (4,207 patients). 
The primary outcome-change in HbA1C levels-showed a strong positive correlation between higher CGM use and greater improvement in glycemic control.
At 12 months, the high-frequency CGM group (frequency 4) had the greatest HbA1C reduction of −1.52 percentage points (95% CI, −1.73 to −1.32), compared with a reduction of only −0.63 percentage points (95% CI, −0.80 to −0.45) in the no CGM group.
Early improvements were evident at approximately 3 months, where all CGM user groups demonstrated significantly greater HbA1C reductions than controls:
Frequency 1: −0.59 percentage points (95% CI, −0.96 to −0.21)
Frequency 2: −0.57 percentage points (95% CI, −1.10 to −0.05)
Frequency 3: −0.79 percentage points (95% CI, −1.25 to −0.34)
Frequency 4: −0.91 percentage points (95% CI, −1.12 to −0.70)
Control group: −0.28 percentage points (95% CI, −0.47 to −0.09)
Most notably, there was no additional improvement beyond 6 months for CGM users in both frequency 2 and 3 groups, suggesting that partial or intermittent use does not confer continued benefits. 
By contrast, patients in frequency 1 and frequency 4 groups had sustained glycemic improvements over the entire follow-up period. 
The combination of frequent CGM use with a GLP-1 RA yielded even greater glycemic benefit, with a mean HbA1C treatment difference of −1.13 percentage points (95% CI, −1.46 to −0.80) compared with non-CGM users.
The present study found that frequent continuous glucose monitoring was associated with significantly better HbA1C outcomes in adults with type 2 diabetes compared with infrequent or no CGM use. The findings reinforce that continuous and consistent CGM use is necessary to achieve long-term glycemic stability and that clinicians should foster adherence and review CGM utilization on a regular basis to optimize therapeutic outcomes.
Reference:
Hirsch IB, Garg SK, Repetto E, et al. Continuous Glucose Monitoring Frequency and Glycemic Control in People With Type 2 Diabetes. JAMA Netw Open. 2025;8(10):e2539278. doi:10.1001/jamanetworkopen.2025.39278 
Disclaimer: This website is primarily for healthcare professionals. The content here does not replace medical advice and should not be used as medical, diagnostic, endorsement, treatment, or prescription advice. Medical science evolves rapidly, and we strive to keep our information current. If you find any discrepancies, please contact us at corrections@medicaldialogues.in. Read our Correction Policy here. Nothing here should be used as a substitute for medical advice, diagnosis, or treatment. We do not endorse any healthcare advice that contradicts a physician's guidance. Use of this site is subject to our Terms of Use, Privacy Policy, and Advertisement Policy. For more details, read our Full Disclaimer here.
NOTE: Join us in combating medical misinformation. If you encounter a questionable health, medical, or medical education claim, email us at factcheck@medicaldialogues.in for evaluation.