Exercise Program Combined or Not With Nutritional intErvention in Adults With tyPe 2 Diabetes (PEP-2)
Overweight, Obesity, Type 2 Diabetes

About this trial
This is an interventional prevention trial for Overweight focused on measuring overweight, obesity, type 2 diabetes, caloric restriction, exercise program, epicardial fat
Eligibility Criteria
Inclusion Criteria:
- Body mass index (BMI) 27-40 kg/m2
- Type 2 diabetes diagnosed since at least 3 months
- High risk of cardiovascular disease : Framingham global cardiovascular risk score for 10 years > 15% or 2 or more of the following risk factors: age > 50years, dyslipidemia or treatment, high blood pressure or treatment, pathologic microalbuminuria or established proteinuria, currently smoking, family history of early cardiovascular disease (< 60 years), inactivity or high waist circumference according to IDF criteria
- HbA1c : 6.0-10.0%
- Stable weight for last 3 months (±3kg) reported or documented
- Stable treatment for diabetes. 4 weeks: blood pressure and dyslipidemia medications. 3 months: glitazones and weight loss drugs the treatment that will be maintained at the same dose during the study; insulin will have been introduced since 4 months at least and previous month dose should be stable defined as a 10% variation or less of total daily units.
Exclusion Criteria:
- Pregnancy, breastfeeding
- Type 1 diabetes
- Secondary diabetes (e.g cystic fibrosis, steroid induced, etc.)
- Recurrent, hypoglycemia without precursor signs or severe hypoglycemia occurred ≥ 2 times for last 12 months
- Renal failure , creatinine clearance < 40 ml/min (MDRD)
- Severe retinopathy or neuropathy that can contra-indicate exercise or expose patient to high risk of complications (e.g wound)
- NYHA classification class III or IV of cardiac insufficiency
- Established coronaropathy
- Non stable ventricular or supra-ventricular arrythmia
- Severe limb atherosclerosis or previous amputation
- Recent (< 12 months) diagnosis of cancer excepted thyroid and skin
- Major mental disease
- Drugs with established effects on weigh such as megace®
Sites / Locations
- Institut de recherches cliniques de Montréal (IRCM)
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Active Comparator
Active Comparator
Optimized usual care
Diet intervention alone
diet intervention and exercise program
participants will attend one visit with the dietician (30mn) and the physical activity specialist (30mn) when they will be given Canadian guidelines pamphlets for physical activity and food consumption. They will also receive a phone call once a month to discuss about issues in guidelines following.
Participants will attend one visit with the physical activity specialist (30mn) when they will receive the physical activity guidelines. Monthly phone call will be make to discuss about issues in physical activity guidelines following.These individuals will also be enrolled in a supervised caloric restriction program. They will have to visit the dietician once a week for the first months and then twice a month for 3 months. The diet intervention will focus on a low fat diet. At each session participants will be weighed and taken the blood pressure.
Participants will attend diet intervention as described for group 2. They will also follow a supervised exercise program three days per week for 4 months. The exercise training is an interval high intensity aerobic (85-90% heart rate reserve) program with resistance exercises (15RM, 2-3 repetitions). Each session will last one hour. At the end of month 1, 2, and 3, all participants will receive the SWA armband for 7 days to record physical activity and estimate energy expenditure. At the end of Month 4, all participants will attend a study visit for repeat baseline testing.