Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07361640

DiaMester Pilot RCT: E-health Lifestyle Program for Type 2 Diabetes

Led by Oslo University Hospital · Updated on 2026-01-23

99

Participants Needed

1

Research Sites

98 weeks

Total Duration

On this page

Sponsors

O

Oslo University Hospital

Lead Sponsor

U

University of Tromso

Collaborating Sponsor

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

DiaMester Pilot RCT: E-health Lifestyle Program for Type 2 Diabetes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent
  • Men and women aged 63; 18 years
  • Diagnosis of type 2 diabetes for 0-6 years based on 2 recorded diagnostic-level tests (HbA1c and/or blood glucose)
  • HbA1c 63; 48 mmol/mol at last routine check within 12 months if on diet alone
  • HbA1c 63; 43 mmol/mol if on oral hypoglycaemic agents or GLP-1 RA treatment
  • Body Mass Index (BMI) over 27 kg/m2
  • Stable body weight during last 6 months with or without weight-reducing drugs
  • Self-reported desire to lose weight
  • Owns a smartphone
Not Eligible

You will not qualify if you...

  • Current insulin use
  • More than 5% weight change or started weight-reducing drugs within last 6 months (including orlistat, bupropion-naltrekson, fenteramin-topiramat, semaglutid, tirzepatid, liraglutid, dulaglutid)
  • Recent routine HbA1c 63; 108 mmol/mol
  • Recent eGFR less than 30 ml/min/1.73 m2
  • Known cancer
  • Myocardial infarction within previous 6 months
  • Severe heart failure (New York Heart Association grade 3 or equivalent)
  • Pregnancy, considering pregnancy, or exclusively breastfeeding
  • Substance abuse (drugs, alcohol)
  • Diagnosed or suspected eating disorders
  • Learning difficulties or unable to understand, speak, and read Norwegian or English
  • Hospitalization for depression or current use of antipsychotic drugs
  • Currently participating in another clinical research trial

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Oslo University Hospital

Oslo, Norway, 0424

Actively Recruiting

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Research Team

A

Anne-Marie Aas, PhD

CONTACT

L

Lise M Østli, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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