GluToTrackGlucose Tolerance Tracking in Non-Insulin Treated Type 2 Diabetes Patients
Physical activity intervention
Behavior+5
+ Diabetes Mellitus
+ Diabetes Mellitus, Type 2
Basic Science Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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
Istituti Clinici Scientifici Maugeri di Pavia
Pavia, ItalyOpen Istituti Clinici Scientifici Maugeri di Pavia in Google Maps