Type 2 Diabetes Clinical Trial
Official title:
Impact of High Milk Product and Calcium Intake During Weight Loss on Markers of Insulin Resistance
Verified date | January 2010 |
Source | University of Calgary |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
The purpose of this study is to determine if increased intake of low-fat milk products and calcium as part of a calorie restricted diet helps achieve a healthier body weight and body composition and decrease blood glucose levels in people with insulin resistance or type 2 diabetes.
Status | Completed |
Enrollment | 49 |
Est. completion date | October 2009 |
Est. primary completion date | April 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Overweight and obese (BMI of 27 to 37 kg/m2) - Impaired glucose tolerance (fasting blood glucose >5.6 mmol/L) or - Type 2 diabetes treated with diet and exercise alone (no medications) - One or more of the following criteria for metabolic syndrome: 1. Hypertriglyceridemia (> 1.70 mmol/L) 2. Low high-density lipoprotein (HDL) cholesterol (< 1.04 mmol/L in men and < 1.30 mmol/L in women) 3. High blood pressure (> 130/85 mm Hg) 4. High waist circumference ( > 94 cm in men, > 80 cm in women) - Weight stable and no changes in exercise in past 3 months Exclusion Criteria: - Type 1 diabetes - Type 2 diabetes treated with oral hypoglycemic agents or insulin - HbA1c > 8% - myocardial infarction or have undergone a cardiovascular intervention within the past three months - Subjects taking fibrate or statins who have had a dose change within the 8 weeks prior to randomization - Liver or pancreas disease - Major gastrointestinal surgeries - Pregnant or lactating - Exhibit alcohol or drug dependence - Taking drugs influencing appetite - Have a milk allergy or lactose intolerance - Following a diet or exercise regime designed for weight loss - Have a body weight greater than 350 lb (weight limit for DEXA instrument) - Chronic use of bulk laxatives, antacids or calcium supplements |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Faculty of Kinesiology, Roger Jackson Centre for Health and Wellness Research | Calgary | Alberta |
Lead Sponsor | Collaborator |
---|---|
University of Calgary |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Weight loss | 12 weeks | No | |
Secondary | Insulin and glucose response | 12 weeks | No | |
Secondary | Inflammatory Markers | 12 weeks | No |
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