Activity and Metformin Intervention in Obese Adolescents

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's60 enrolled

Overview

The purpose of this study is to assess the sustainability of a two-year intervention aimed at improving body mass index (BMI) and metabolic and vascular health in obese youth. The study will compare lifestyle changes with diet and exercise alone with changes in lifestyle in combination with metformin medication. An initial intensive exercise program will also be compared with a standard exercise program. Hypothesis: Metformin therapy in combination with intensive lifestyle intervention in obese children and adolescents will be associated with reduced rate of weight gain, improved BMI, body composition, physical activity, physical fitness, insulin sensitivity, blood lipid profiles, adipocytokines and vascular function.

This study will assess the sustainability of a two-year intervention and the degree of improvement in body mass index (BMI) and reduction in risk factors for type 2 diabetes and diabetes related cardiovascular disease, as well as evaluating the additive effect of metformin (as GlumetzaTM 500 mg Extended Release Tablets) and comparing an initial intensive exercise program with a standard exercise program. The study will recruit obese youth who are at risk for type 2 diabetes and cardiovascular disease.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

Conditions

Obesity Type 2 Diabetes

Interventions

Metformin and standard exerciseDRUG

Metformin 1500 mg daily for 2 years

Metformin Intensive exerciseDRUG

Metformin 1500 mg daily for 2 years

Placebo Standard exerciseBEHAVIORAL

Standard exercise

Intensive exerciseBEHAVIORAL

Placebo Intensive exercise

Eligibility

Sex: ALLMin age: 10 YearsMax age: 16 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Obese adolescents defined as BMI greater than the 95th percentile for age and gender * Metformin naive subjects Exclusion Criteria: * Elevated fasting plasma glucose ≥ 6.0 mmol/L * 2 hour plasma glucose ≥ 11.1 mmol/L after a standard glucose load * A1C \> 6.0% * Medication other than "over the counter" drugs, oral contraceptive pill or thyroid hormone replacement * Smoking * Pregnancy * Renal insufficiency (serum creatinine \> the upper limit of normal) * Hepatic dysfunction (\> 1.5 times the upper limit of normal for AST and ALT) * Latex Allergy * Hypersensitivity to metformin or its ingredients * Breast feeding * Subjects with a history of lactic acidosis * Abnormal creatinine clearance * HIV, HBV, and HCV infections * Drug and alcohol abuse * Severe mental disorders * Subjects who are planning radiologic exams involving in i.v. injection of iodinated contract materials * Participation in another clinical trial * Significant history or presence of cardiovascular, pulmonary, gastrointestinal, immunologic, endocrine, neurologic disorders * Malignant diseases * Previous exposure to any pharmaceutical antidiabetic agent

Activity and Metformin Intervention in Obese Adolescents

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes