Testing a lifestyle program to prevent type 2 diabetes in Brazilian adults

Trial details

Who runs it

Beneficência Portuguesa de São Paulo

Trial code

NCT06426277

Record updated

25 June 2026

Original description

The aim of this multicenter, randomized controlled trial is to assess the effectiveness of the Brazilian Diabetes Prevention Program (delivered face-to-face or via e-health) in preventing type 2 diabetes (T2D) in at least 1,305 adults at high risk of T2D over a 3-year follow-up period. Our outcomes include the incidence of T2D, body weight (kg), BMI, glycemic biomarkers, use of antidiabetic drugs, the proportion of individuals achieving controlled glycemia or HbA1c levels without medication, diet quality, moderate-to-vigorous physical activity (min/week), prevalence of physical inactivity, sleep quality, perceived stress, alcohol consumption, smoking, and quality of life. In addition, social, cultural, educational, and geographical factors at the community level will be analyzed throughout the follow-up to determine their association with the incidence of T2D.Read full original descriptionShow less

Effectiveness of the Diabetes Prevention Program on the Incidence of Type 2 Diabetes Mellitus Among Brazilian Individuals: Randomized Clinical Trial (PROVEN-DIA Study)

The aim of this multicenter, randomized controlled trial is to assess the effectiveness of the Brazilian Diabetes Prevention Program (delivered face-to-face or via e-health) in preventing type 2 diabetes (T2D) in at least 1,305 adults at high risk of T2D over a 3-year follow-up period. Our outcomes include the incidence of T2D, body weight (kg), BMI, glycemic biomarkers, use of antidiabetic drugs, the proportion of individuals achieving controlled glycemia or HbA1c levels without medication, diet quality, moderate-to-vigorous physical activity (min/week), prevalence of physical inactivity, sleep quality, perceived stress, alcohol consumption, smoking, and quality of life. In addition, social, cultural, educational, and geographical factors at the community level will be analyzed throughout the follow-up to determine their association with the incidence of T2D.

Inclusion: Be 18 years or older (no maximum age for being eligible); Have a body mass index (BMI) between 18,5 and 34,9kg/m²; Have, at least, one electronic device (includes any of the following devices):; Computer; Laptop/notebook; Tablet; Smartphone; Have access to internet (broadband, 3G, 4G, 5G, among others) Without previous nutritional counseling (within the 6 months prior to recruitment/randomization/intervention) Without supervision by a Physical Education Professional (Personal Trainer) in the past 6 months; Living near the research center (at maximum 60 minutes); Diagnosis of prediabetes defined as two HbA1c measurements between 5.7% and 6.4% collected 7 to 90 days apart.

Exclusion: Continuous use of the following medications:; Corticosteroids other than topical, ophthalmic, or inhaled preparations Antineoplastic agents Psychoactive agents Other medications; Underlying disease likely to limit life expectancy and/or increase the risk of interventions influencing the risk of developing T2D; Diagnosis of Renal Disease; Diagnosis of Pulmonary Disease; Gastrointestinal Disease; Secondary prevention for Cardiovascular Disease; Endocrine Diseases; Uncontrolled Hypertension; Diagnosis of Polycystic Ovary Syndrome (self-reported); Patients undergoing treatment for Tuberculosis (except those using isoniazid [INH] as prophylaxis); Presence of diseases that may severely reduce life expectancy or the ability to participate in the study; Severe psychiatric disorders that, in the opinion of the clinical team, hinder participation in the program; Congestive Heart Failure (CHF) with a New York Heart Association Functional Class (NYHA) > 2; Participant from the pilot Randomized Clinical Trial (Brazilian Diabetes Prevention Program: Pilot Study (PROVEN-Dia), NCT05689658); Diagnosis of Diabetes Mellitus (including current or recent use, within three months, of glucose-lowering medication); Weight loss exceeding 10% in the last 6 months (except postpartum-related); Pregnant or breastfeeding women; Acute or chronic excessive alcohol consumption; Need for referral to a cardiologist according to the Physical Activity Readiness Questionnaire (PAR-Q); Current or recent participation (within the last six months) in another clinical trial that impacts the interventions and/or is associated with the study outcomes (in case of doubt, contact the coordinating center); Likely relocation away from the research collaborating center within the next 3 years; Another household member is a participant or a team member of the PROVEN-DIA study; Unwillingness to accept treatment assignment by randomization and/or refusal to participate in the study (signing the Informed Consent Form).

ClinicalTrials.gov NCT06426277