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CompletedNCT04331444Updated Oct 12, 2023

Steno2tech - Continuous Glucose Monitoring and Type 2 Diabetes.

An interventional study of CGM and training course in Type 2 Diabetes Treated With Insulin, sponsored by Steno Diabetes Center Copenhagen. Completed at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-10-12.

Sponsored by Steno Diabetes Center Copenhagen · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
96
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The overall objective of this research study is to examine the effectiveness of the use of CGM vs. SMBG in persons with insulin-treated type 2 diabetes on glycemic variables and patient reported outcomes on treatment satisfaction, health behavior and wellbeing. The independent effect of peer-support will also be studied.

Read the detailed description

The prevalence of type 2 diabetes is increasing. Although medical treatment options have increased, still less than a third obtain their optimal glycemic goal. The use of continuous glucose monitoring (CGM) in persons with type 1 diabetes has shown to be the most important driver for improvement in glycemic control-even more than insulin-pump therapy-but the use of technology in type 2 diabetes are not yet reimbursed and has been investigated in very few studies.

The study will be a single center, prospective, randomized, open-labelled, three-armed study with the randomization 2:1:2 in group A with CGM, group B with CGM and peer-support, group C as a control group with SMBG. The study will run for 12 months and will include 100 adult participants with insulin-treated type 2 diabetes, treated at the outpatient clinic at Steno Diabetes Center Copenhagen. Recruitment will begin in August 2020 and end in May 2022. Final 12-month follow-up is anticipated to be in July 2023.

The study is investor-initiated. The primary investigator (Nanna Lind, PhD. Student) will be responsible for execution of this study under guidance by the sponsor Kirsten Nørgaard. Results will be published in international peer-reviewed journals.

Our study will provide evidence of the effectiveness of the use of CGM in the treatment for type 2 diabetes, potentially shaping clinical guidelines for SMBG frequency and timing as well as use of technology in type 2 diabetes with an impact on both healthcare and healthcare costs.

02

Conditions studied

  • Type 2 Diabetes Treated With Insulin

Keywords

  • Type 2 diabetes
  • Continuous glucose monitoring
  • Insulin-treated
  • RCT
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 96 is above the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Steno Diabetes Center Copenhagen is the lead sponsor of 111 studies on the registry; 22 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Type 2 diabetes according to clinical definitions
  • Treated with insulin injections at least once daily on top of diet and exercise recommendations. Insulin therapy has been used for at least 12 months. Can be additionally treated with one or more different oral antidiabetic drugs (except sulfonylurea), and/or glucagon-like-peptide 1 (GLP-1) analogues
  • Attending the outpatient clinic at Steno Diabetes Center Copenhagen for at least 12 months
  • Age ≥ 18 years
  • HbA1c > 58 mmol/mol (7.5%) at two consecutively measurements over at least 3 months
  • Willing to use possible interventions; to perform self-monitoring of blood glucose (SMBG) as requested by the investigators AND to use CGM continuously without calibration for a 12-month period.
  • Willing to intensify non-medical and medical treatment to achieve better glucose control.

Exclusion criteria

Exclusion Criteria:

  • Inability to understand the patient information and give informed consent
  • Not speaking and understanding Danish
  • Treatment with sulfonylurea (SU) during the last 3 months before study start
  • New antidiabetic treatment the last three months
  • Use of systematic corticosteroids
  • Visual impairment
  • Severe skin allergy for adhesive tape to the patch of CGM or other skin condition that inhibits the use of a CGM device
  • Comorbidity which does not allow lowering of HbA1c to 53 mmol/mol (7.0%)
  • Hypoglycemic unawareness
  • Impaired renal disease with eGFR \< 45 ml/min/1.73m2
  • Conditions that impact the stability of a HbA1c measurement (chronic liver disease, haemoglobinopathy, anemia etc.)
  • Known or suspected alcohol or drug abuse
  • Already using Flash glucose monitoring (Libre) or CGM
  • Enrolled in another clinical study
  • Pregnancy, intend to become pregnant, breastfeeding or not using adequate contraceptive methods
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
96 participants (actual)

Study arms

  • Experimental
    Group A, CGM

    Addition of a calibration free real-time CGM in 12 months in persons with type 2 diabetes treated with insulin. The participants will participate in a training course that will include the influence of different food items and exercise on glucose levels, how to measure SMBG correctly. Furthermore, participants in group A (intervention) will, in similarity to the HCPs, receive a CGM-education and training session led by the study investigator and will be interactive and hands-on, using case studies. The training session will include spoken and written instructions on how to insert and wear the CGM device and how to interpret the CGM information to better understand the relation between participants blood glucose and their diabetes self-management.

    Device: CGM · Behavioral: training course

  • Experimental
    Group B, CGM + peer-support

    Addition of a calibration free real-time CGM in 12 months in persons with type 2 diabetes treated with insulin plus 3 sessions of peer-support in groups of 6 participants. The participants will participate in a training course that will include the influence of different food items and exercise on glucose levels, how to measure SMBG correctly. Furthermore, participants in group B (intervention incl. peer-support) will, in similarity to group A, receive a CGM-education and training session. The training and CGM-course for participants in group B are similar to the course for group A with the addition of three peer-support sessions. The approach will be participatory and adaptable to allow flexibility in the content of the peer-support sessions and involving customized use of participatory methods i.e. dialogue tools and exercises.

    Device: CGM · Behavioral: training course · Behavioral: Peer-support

  • Active comparator
    Group C, SMBG

    Standard self-monitoring of blood glucose according to standard guidelines, in 12 months. The participants will participate in a training course that will include the influence of different food items and exercise on glucose levels, how to measure SMBG correctly.

    Behavioral: training course

Interventions

  • DeviceCGM

    Using the CGM during the entire study period of 12 months.

    Also known as: Continuous glucose monitoring

  • Behavioraltraining course

    The participants in the three groups will attend a three-hour training course with different content depending on the group allocation. The aim of this training course is to ensure that the participants have the knowledge, support and confidence to work collaboratively with their HCPs to increase TIR and decrease HbA1c.

  • BehavioralPeer-support

    The peer-support will be facilitator-led by the primary investigator with peer exchange in group sessions (3 sessions over the study period, 3 hours per session) with 6-8 participants in every group.

    Also known as: Group sessions

06

What researchers measure

Primary outcomes

  1. Difference between change in TIR (3.9-10 mmol/l) in percent, assessed via blinded CGM device, between CGM group (A) and SMBG group (C)

    Percent

    Time frame: from baseline to 12 months

Secondary outcomes

  1. Difference between change in HbA1c between the CGM group (A) and the SMBG group (C)

    mmol/mol

    Time frame: from baseline to 12 months

  2. Difference between change in mean sensor glucose concentration measured by 2 weeks blinded CGM between the CGM group (A) and the SMBG group (C)

    mmol/l

    Time frame: from baseline to 12 months

  3. Difference between change in time below range (TBR) (< 3.9 mmol/l, < 3.0 mmol/l), in percent, measured by 2 weeks blinded CGM between the CGM group (A) and the SMBG group (C)

    Percent

    Time frame: from baseline to 12 months

  4. Difference between change in time above range (TAR) (>10 mmol/l, > 13.9 mmol/l), in percent, measured by 2 weeks blinded CGM, between the CGM group (A) and the SMBG group (C)

    Percent

    Time frame: from baseline to 12 months

  5. Difference between change in glycemic variability (SD, Coefficient of variance and others), measured by 2 weeks blinded CGM between the CGM group (A) and the SMBG group (C)

    Percent

    Time frame: from baseline to 12 months

  6. Difference between change in number of severe hypoglycemic episodes between the CGM group (A) and the SMBG group (C)

    number

    Time frame: from baseline to 12 months

  7. Difference between change in insulin dose between the CGM group (A) and the SMBG group (C)

    units

    Time frame: from baseline to 12 months

  8. Difference between change in BMI between the CGM group (A) and the SMBG group (C)

    weight and height will be combined to report BMI in kg/m\^2

    Time frame: from baseline to 12 months

  9. Difference between change in antidiabetic medicine between the CGM group (A) and the SMBG group (C)

    (new medication, change in doses, discontinuation of medicine)

    Time frame: from baseline to 12 months

  10. Difference between change in patients related outcome measures on general wellbeing, between the CGM group (A) and the SMBG group (C)

    measured by the questionnaire WHO-5

    Time frame: from baseline to 12 months

  11. Difference between change in patients related outcome measures on diabetes-related distress, between the CGM group (A) and the SMBG group (C)

    measured by the Diabetes Distress Scale

    Time frame: from baseline to 12 months

  12. Difference between change in patients related outcome measures on hypoglycemia fear between the CGM group (A) and the SMBG group (C)

    measured by the short form Hypoglycemia Fear Survey

    Time frame: from baseline to 12 months

  13. Difference between change in patients related outcome measures on diabetes treatment satisfaction between the CGM group (A) and the SMBG group (C)

    measured by the Diabetes Treatment Satisfaction Quenstionnaire

    Time frame: from baseline to 12 months

  14. Difference between change in patients related outcome measures on satisfaction with glucose monitor between the CGM group (A) and the SMBG group (C)

    measured by the Glucose Monitoring Satisfaction Scale

    Time frame: from baseline to 12 months

  15. Difference between change in health behavior regarding exercise between the CGM group (A) and the SMBG group (C)

    measured by the Swedish National Board of Health and Welfare questionnaire for Physical Activity

    Time frame: from baseline to 12 months

  16. Difference between change in health behavior regarding diet between the CGM group (A) and the SMBG group (C)

    measured by the Danish Perceived Dietary Adherence questionnaire

    Time frame: from baseline to 12 months

  17. Difference between change in health behavior regarding anti-diabetic medication adherence between the CGM group (A) and the SMBG group (C)

    measured by the Danish Medical Adherence Scale

    Time frame: from baseline to 12 months

  18. Difference between change in TIR, assessed by 2 weeks blinded CGM device, and HbA1c between the CGM groups (without peer-support group A and with peer-support group B)

    Percent

    Time frame: from baseline to 12 months

  19. Difference between change in general wellbeing between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the questionnaire WHO-5

    Time frame: from baseline to 12 months

  20. Difference between change in diabetes-related distress between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Diabetes Distress Scale

    Time frame: from baseline to 12 months

  21. Difference between change in hypoglycemia fear between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the short form Hypoglycemia Fear Survey

    Time frame: from baseline to 12 months

  22. Difference between change in glucose monitoring satisfaction between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Glucose Monitoring Satisfaction Scale

    Time frame: from baseline to 12 months

  23. Difference between change in diabetes treatment satisfaction between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Diabetes Treatment Satisfaction Quenstionnaire

    Time frame: from baseline to 12 months

  24. Difference between change in health behavior regarding exercise between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Swedish National Board of Health and Welfare questionnaire for Physical Activity

    Time frame: from baseline to 12 months

  25. Difference between change in health behavior regarding diet between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Danish Perceived Dietary Adherence questionnaire

    Time frame: from baseline to 12 months

  26. Difference between change in health behavior regarding anti-diabetic medication adherence between the CGM groups (without peer-support group A and with peer-support group B)

    measured by the Danish Medical Adherence Scale

    Time frame: from baseline to 12 months

  27. Difference in mean number of days of CGM use between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    days

    Time frame: from baseline to 12 months

  28. Difference in HbA1c baseline between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    mmol/mol

    Time frame: from baseline to 12 months

  29. Difference in age between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    in years

    Time frame: from baseline to 12 months

  30. Difference in diabetes duration between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    in years

    Time frame: from baseline to 12 months

  31. Difference in C-peptide between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    pmol/l

    Time frame: from baseline to 12 months

  32. Difference in education level between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    Percent

    Time frame: from baseline to 12 months

  33. Difference in social status between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    measured by civil status and occupation

    Time frame: from baseline to 12 months

  34. Difference in ethnicity between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    white/non-white

    Time frame: from baseline to 12 months

  35. Difference in medicine used between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    Time frame: from baseline to 12 months

  36. Difference in change in health behavior regarding to diet between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    measured by the Danish Perceived Dietary Adherence questionnaire

    Time frame: from baseline to 12 months

  37. Difference in change in health behavior regarding to exercise between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    measured by the Swedish National Board of Health and Welfare questionnaire for Physical Activity

    Time frame: from baseline to 12 months

  38. Difference in change in health behavior regarding to medication adherence between individuals achieving TIR> 70% vs TIR< 70% within the CGM groups (group A+B)

    measured by the Danish Medical Adherence Scale

    Time frame: from baseline to 12 months

  39. Correlation between mean number of SMBG/day and time points for SMBG in the study period and improvement in HbA1c, in TIR, in TBR, in TAR within the control group C

    Time frame: from baseline to 12 months

  40. Difference between number of participants using CGM vs. not using CGM increasing 5 % or more in TIR

    number

    Time frame: from baseline to 12 months

Other outcomes

  1. Evaluating which blood glucose measured by SMBG best reflect TIR

    (fasting, pre-prandial or postprandial)

    Time frame: from baseline to 12 months

07

Study locations

1 site
  • Steno Diabetes Center Copenhagen
    Gentofte, Hovedstaden 2820, Denmark
08

References and documents

Publications

  • Lind N, Lindqvist Hansen D, Saetre Rasmussen S, Norgaard K. Real-time continuous glucose monitoring versus self-monitoring of blood glucose in adults with insulin-treated type 2 diabetes: a protocol for a randomised controlled single-centre trial. BMJ Open. 2021 Jan 15;11(1):e040648. doi: 10.1136/bmjopen-2020-040648. PubMed 33452188 ↗

Individual participant data

Plan to share: No — Study results, positive, negative and inconclusive findings, will be presented at national and international scientific meetings and published in at least three scientific papers in international scientific peer-reviewed journals and through the PhD thesis. After conclusion of the study, a final report will be generated and sent to the Regional Scientific Ethics Committee (RVK). The study protocol will furthermore be published at www.clinicaltrial.gov.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04331444
Lead sponsor
Steno Diabetes Center Copenhagen
Responsible party
Nanna Lind (RN, MSc. in nursing, Steno Diabetes Center Copenhagen) — Principal investigator
First posted
Apr 2, 2020
Start date
Aug 1, 2020
Primary completion
Jul 1, 2023
Completion
Jul 1, 2023
Last update
Oct 12, 2023

Study contacts

Nanna Lind, RN MSc
principal investigator · Steno Diabetes Center Copenhagen

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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