Type 2 Diabetes (T2D) Clinical Trials

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DiaMester: E-health Lifestyle Program for Improved Self-management and Remission of Type 2 Diabetes - a Pilot RCT

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This registration covers a pilot for a 3-armed parallel-group randomized controlled trial (RCT) that will evaluate the efficacy of DiaMester, a Norwegian e-health programme designed to improve self-management and induce clinically meaningful weight loss, and thereby potential remission in adults with type 2 diabetes (T2D).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Written informed consent

• Men and women aged ≥ 18 years

• Type 2 diabetes of duration 0-6 years (diagnosis based on 2 recorded diagnostic-level tests, HbA1c and/or blood glucose)

• HbA1c ≥ 48 mmol/mol at the last routine clinical check, within last 12 months if on diet alone

• HbA1c ≥ 43 mmol/mol if on treatment with oral hypoglycaemic agents or GLP-1 RA treatment

• Body Mass Index (BMI) \>27 kg/m2

• Stable body weight during the last 6 months with or without the use of weight-reducing drugs

• Self-reported desire to lose weight

• Owns a smartphone

Locations
Other Locations
Norway
Oslo University Hospital
RECRUITING
Oslo
Contact Information
Primary
Anne-Marie Aas, PhD
a.m.aas@medisin.uio.no
+47 47302912
Backup
Lise M Østli, MSc
l.m.ostli@medisin.uio.no
+47 97180196
Time Frame
Start Date: 2026-01-14
Estimated Completion Date: 2027-12
Participants
Target number of participants: 99
Treatments
Experimental: 1
E-health program with LCD
Experimental: 2
E-health program without LCD
No_intervention: 3
Standard care, but with continuous glucose monitoring (CGM) for 10 days at baseline and 1 year.
Related Therapeutic Areas
Sponsors
Collaborators: Abel Technologies AS, University of Oslo, Diabetes Wellness Norway, Norwegian Diabetes Association, University of Tromso, The Dam Foundation
Leads: Oslo University Hospital

This content was sourced from clinicaltrials.gov