Recruiting

GluToTrackGlucose Tolerance Tracking in Non-Insulin Treated Type 2 Diabetes Patients

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Physical activity intervention

Behavioral
Who is being recruted

Behavior+5

+ Diabetes Mellitus

+ Diabetes Mellitus, Type 2

From 40 to 70 Years
+11 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Basic Science Study

Interventional
Study Start: May 2025
See protocol details

Summary

Principal SponsorEnea Parimbelli
Study ContactEnea Parimbelli
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2025

Actual date on which the first participant was enrolled.

Diabetes, particularly Type 2 Diabetes (T2D), is a rapidly growing health issue worldwide. This study aims to support people with T2D who are not using insulin by helping them track how their bodies handle glucose. The focus is on how lifestyle changes, like exercise and diet, can not only manage but potentially reverse the progression of T2D. The study uses technology, such as continuous glucose monitoring (CGM) devices and smartphones, to provide real-time feedback and education. This approach can empower patients to better manage their condition and help healthcare providers monitor disease progression and treatment effectiveness. In the study, 20 participants aged between 40 and 70 years who are not physically active and do not use insulin will use wearable technology, including CGM devices and activity trackers. For one week, they will continue their usual sedentary lifestyle, and during the second week, they will increase their activity to at least 10,000 steps per day. This involves replacing sitting with light walking, totaling at least 150 minutes of activity per week. At the start and end of each week, participants will undergo a meal test to measure glucose, insulin, and C-peptide levels in their blood. This will help evaluate how the increased physical activity impacts their glucose tolerance, providing insights into the effectiveness of lifestyle changes in managing T2D.

Official TitleA Participatory Approach to Support Glucose Tolerance Tracking in Real-Life of Patients With Type 2 Diabetes
NCT06864546
Principal SponsorEnea Parimbelli
Study ContactEnea Parimbelli
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

20 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Basic Science Study

Basic science studies help researchers understand how the body works or how a disease develops. They don't test treatments, but they build the foundation for future therapies.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 40 to 70 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorDiabetes MellitusDiabetes Mellitus, Type 2Endocrine System DiseasesMetabolic DiseasesMotor ActivityNutritional and Metabolic DiseasesGlucose Metabolism Disorders

Criteria

4 inclusion criteria required to participate
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%.

7 exclusion criteria prevent from participating
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);

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Study participants will be monitored for two weeks with a CGM device and an activity tracker. During the first week, participants will follow their usual daily routine, while in the second week, subjects will be asked to engage in daily physical activity, consisting of walking

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Istituti Clinici Scientifici Maugeri di Pavia

Pavia, ItalyOpen Istituti Clinici Scientifici Maugeri di Pavia in Google Maps
Recruiting
One Study Center
GluToTrack | Glucose Tolerance Tracking in Non-Insulin Treated Type 2 Diabetes Patients | PatLynk