Tracking glucose tolerance in patients with type 2 diabetes using technology

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to enhance the management of type 2 diabetes through a participatory e-health approach that utilizes continuous glucose monitors (CGM) and other health tracking devices. By collecting real-time health data from patients, the study will develop an easy-to-use tool for tracking metabolic status and analyze the relationship between lifestyle changes and glucose levels. The focus is on sedentary individuals with type 2 diabetes who are not on insulin treatment, promoting lifestyle interventions to improve their health outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Non-insulin treated T2D diagnosis (not treated at all or only with metformin);
* Physically inactive (less than 150 minutes/week of moderate physical activity);
* Age between 40 and 70;
* HbA1c below 8.5%.

Exclusion Criteria:

* Diabetes diagnosis less than 3 years before the study initiation;
* Pregnancy;
* Symptomatic heart disease, e.g. history of myocardial infarction, coronary bypass, stenting procedure, angina, or any ischemic cerebrovascular event;
* Use of a medication that significantly impacts glucose metabolism (oral steroids);
* Use of a medication that significantly lowers heart rate (beta blockers, reserpine, guanethidine, methyldopa, clonidine, cimetidine, digitalis, calcium channel blockers, amiodarone, antiarrhythmic drugs, or lithium);
* Atrial fibrillation;
* Use of an electronic pacemaker.

Where it's running

• Istituti Clinici Scientifici Maugeri di Pavia
  Pavia, Pavia, Italy Recruiting

Study contacts

• Study coordinator: Enea Parimbelli
• Email: enea.parimbelli@unipv.it
• Phone: +39 0382 9895981

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.