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Efficacy of the digital therapeutic glucura combined with CGM in the treatment of type 2 diabetes: a randomised controlled trial over 6 months

In brief

Adding Glucura to intermittent CGM lowered HbA1c by 0.46 percentage points

In a 6-month trial of 327 adults with non-insulin-treated type 2 diabetes, HbA1c fell 0.80 percentage points with Glucura plus intermittent continuous glucose monitoring, versus 0.30 points with monitoring and standard care; weight loss was also greater. Both groups used monitoring every three months, and the open-label, manufacturer-funded study leaves longer-term benefit and durability uncertain.

Journal
Diabetologia (Q1)
Published
1 October 2026
Study design
Randomized controlled trial
Evidence level
Level 1, High (CEBM 1b)
Authors
Guido Freckmann, Inke R König, Hanna Grube, Maren Vens, Oliver Witt, Vanessa Kappelmeier, et al.
PMID
42820970
DOI
10.1007/s00125-026-06880-6

Why clinicians should know about it

  • Picked for Family Practice (paper of the day, 2 October 2026): Greater HbA1c reduction with digital therapeutic plus CGM

Abstract

AIMS/HYPOTHESIS: CGM is increasingly recommended for non-insulin-treated type 2 diabetes according to the ADA Standards of Care 2026. However, its clinical benefit in high-quality standard care remains limited. This study evaluated whether addition of the digital therapeutic glucura, which delivers personalised lifestyle intervention and self-management guidance, improves glycaemic outcomes beyond CGM and standard care. METHODS: The study was a 6-month, multicentre, open-label RCT conducted at 24 sites in Germany (ID: DRKS00032537). Adults (≥18 years) with non-insulin-treated type 2 diabetes (HbA1c 53-97 mmol/mol [7.0-11.0%], BMI≥25 kg/m2) receiving standard care were randomly assigned (1:1) by centralised stratified block randomisation to glucura or a control app. Participants and study personnel were not masked to group assignment. Both groups used intermittent CGM every 3 months during the study. CGM sensors were not used prior to the study. The primary endpoint was the change in HbA1c from baseline to 6 months. Secondary outcomes included weight change and patient-centric measures. RESULTS: Of 327 randomised participants (intervention: n=165; control: n=162), 320 were analysed (ITT population). The standalone CGM control group improved HbA1c levels by 3.3 mmol/mol (0.30 percentage points); however, the intervention group showed greater reductions of 8.7 mmol/mol (0.80 percentage points) with an adjusted difference of -5 mmol/mol (-0.46 percentage points; 95% CI -7, -3 mmol/mol; p=0.00003). Within the intervention group, more participants achieved HbA1c targets (<53 mmol/mol [<7.0%]: 55% vs 31%, OR 3.38, exploratory p=0.0002; <48 mmol/mol [<6.5%]: 27% vs 7%, OR 6.63, exploratory p=0.0001). The mean weight loss was also greater in the intervention group (4.11% vs 1.79%, p<0.0001). Significant improvements in mental health and diabetes-related distress were also observed. The positive effects were consistent across all subgroups. No device-related serious adverse events were observed. CONCLUSIONS/INTERPRETATION: In non-insulin-treated type 2 diabetes, CGM plus standard care yielded less metabolic benefit than CGM combined with glucura. The combination of glucura and CGM also translated into improvements beyond glycaemic management. Trial registration German Clinical Trials Register DRKS00032537 Funding The study was funded by Perfood Laboratories GmbH.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.