- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00852475
Comparative Effects of 2 Diets in Veterans With the Metabolic Syndrome (MUFAPUFA)
Comparative Effects of Two Popular Diets in Veterans With the Metabolic Syndrome
The purpose of the study is to examine the effects of 2 commonly used diets, a Mediterranean monounsaturated fatty acid enriched (MUFA) or AHA polyunsaturated (PUFA) enriched diet combined with the VA Managing Overweight/Obesity for Veterans Everywhere (MOVE!) program so as to determine which one is superior in reducing cardiometabolic risk factors associated with Metabolic Syndrome. The risk factors considered include lipids and lipoproteins, inflammatory markers such as CRP and adiponectin, endothelium-dependent flow-mediated vasodilatation (FMD) and the postprandial lipid responses to a meal.
Cardiometabolic risk factors will be determined by measuring several cardiovascular risk associated parameters including:
Biochemical measurements of lipids and inflammatory markers, body composition and VO2max (Specific Objective 1, Descriptive).
Postprandial response to a meal challenge and endothelial vasoreactivity (FMD) assessed by BART (Specific Objective 2, Physiological).
Determination of the effects on postheparin lipases and transfer protein activity, visceral adipose tissue (VAT) and homeostasis model assessment-estimated insulin resistance (HOMA-IR) (Specific Objective 3, Mechanistic)
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maryland
-
Baltimore, Maryland, United States, 21201
- VA Maryland Health Care System, Baltimore
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Presence of 3 or more of the following):
- Waist circumference >102 cm in men or >88 cm women
- Treated Hypertension or Untreated Blood pressure >130/85 and < 160/100 mm Hg
- Treated Hyperglycemia or Untreated Fasting blood glucose (FBG) >100 mg/dL (based on 2006 guidelines)
- Treated Hyperlipidemia or Untreated Triglycerides > 150 mg/dL
- HDL-C < 40 mg/dL men < 50 mg/dL women
Exclusion Criteria:
- Decompensated heart failure (NYHA Class IV);
- Severe Pulmonary disease (Unable to walk on a treadmill at 2.5 mph or greater);
- Chronic renal insufficiency (Cr > 2.5 mg/dL)
- Treated diabetes mellitus with FBG > 180 mg/dL or HbA1C >9g %
- Hematologic or malignant disorders
- Treated SBP >160 mmHg and/or DBP > 95 mmHg ;
- Treated TG > 250 mg/dL
- Use of systemic vasodilators (e.g., nitrates)
- Morbid Obesity (BMI > 50 kg/m2)
- Endocrine (thyroid) or metabolic disorders (unless treated and under control)
- Alcohol consumption greater than (2) 4-ounce glasses of table wine, (2) 12-oz bottles of beer or 2 shots of spirits in men or women
- Active IV drug abuse within the past 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: MUFA
Assignment to monounsaturated enriched diet with exercise.
This represents the MUFA MOVE! program
|
MUFA MOVE!diet and exercise program
|
|
Active Comparator: PUFA
Assignment to polyunsaturated enriched diet with exercise.
This represents the PUFA MOVE! program
|
PUFA MOVE! diet and exercise program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Weight Changes in Veterans With MetS.
Time Frame: 6 months from Baseline
|
6 months from Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Endothelium-dependent FMD Assessed by the Brachial Artery Reactivity Test (BART) at Rest .
Time Frame: 6 months from Baseline
|
Ultrasonographic imaging of the brachial artery (BART) was used to assess endothelium-dependent flow-mediated vasodilation (FMD) in participants at rest.
To do this,the blood pressure cuff is inflated to 200 mm Hg and kept inflated for 5 minutes.
On immediate release of the cuff, the brachial artery was imaged within 1 minute after cuff release.
|
6 months from Baseline
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Michael Miller, MD, VA Maryland Health Care System, Baltimore
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CARA-030-08F
- HP-00040456 (Other Identifier: Univ. of MD School of Med IRB)
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