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Preventing Obesity Using Novel Dietary Strategies

Primary Purpose

Cardiovascular Diseases, Heart Diseases, Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Four Diets Differing in Macronutrient Composition
Diets Low in Saturated Fat
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Only accepting participants in the Boston, Massachusetts or Baton Rouge, Louisiana area Between the ages of 30 - 70 Willing to modify eating pattern according to instructions Overweight or obese and in good health with a BMI of 25-40 Committed to a long-term weight loss and maintenance program Willing to attend multiple weight loss group sessions Willing to increase activity level Exclusion Criteria: Pregnant, planning to become pregnant, or are breastfeeding Unwilling to participate in the schedule of group sessions and individual visits Unstable or recent onset of heart disease or any other serious illness Cannot change diet due to medical or other reasons Planning to leave the area prior to the anticipated end of participation Current participation in another clinical trial with an intervention that affects weight change Have diabetes that is treated with insulin or hypoglycemic oral medicines Diagnosis of psychiatric or emotional problems within 6 months of study Currently have an eating disorder Have hypothyroidism Have an unstable weight

Sites / Locations

  • Pennington Biomedical Reseach Center, Louisiana State University
  • Harvard University School of Public Health

Outcomes

Primary Outcome Measures

Change in body weight (measured at Year 2)

Secondary Outcome Measures

Body fat
BMI
Waist circumference
Visceral fat
Hepatic and skeletal muscle
Psychological factors from diet
Major cardiovascular risk factors
Prevalence of the metabolic syndrome (measured at Year 2)

Full Information

First Posted
November 13, 2003
Last Updated
January 29, 2013
Sponsor
Brigham and Women's Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00072995
Brief Title
Preventing Obesity Using Novel Dietary Strategies
Official Title
Preventing Overweight Using Novel Dietary Strategies (Pounds Lost)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
December 2007 (Actual)
Study Completion Date
December 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test the effectiveness for weight loss and weight maintenance of four diets differing in macronutrient composition: moderate in fat (40 percent energy) with two different protein levels (15 percent and 25 percent), and low in fat (20 percent energy), also with 15 percent and 25 percent protein levels. The study is only accepting participants in the Boston, Massachusetts or Baton Rouge, Louisiana area. For further enrollment information in Boston or Baton Rouge, see Eligibility Criteria or Design Narrative.
Detailed Description
BACKGROUND: Obesity is a growing problem whose importance is reflected in the resources that are expended each year by a large section of the population on weight reduction drugs and therapies. Although numerous weight loss diets are available, there is little agreement in the scientific literature or the lay press as to the amount of fat, protein, and carbohydrates that would comprise the most efficacious diet for weight loss and long term weight loss retention. Reliable information about the effectiveness of low calorie diets with differing macronutrient composition is clearly needed and of paramount importance to inform the choice of a weight reduction diet. DESIGN NARRATIVE: The study tests the effectiveness for weight loss and weight maintenance of four diets differing in macronutrient composition: moderate in fat (40% energy) with two different protein levels (15% and 25%), and low in fat (20% energy), also with 15% and 25% protein levels. The moderate-fat diet will be patterned after a Mediterranean diet. All four dietary approaches will be low in saturated fat, and will involve reduction in total energy intake. Each diet is deemed practical and suitable for public health recommendations, and each would be expected to have a favorable effect on cardiovascular disease risk factors. All participants will receive a state-of-the-art behavioral therapy program standardized across the two centers in Boston and Baton Rouge. An estimated 800 men and women, age 30-70 years, body mass index (BMI) 25-40 kg/m2, will be randomized among the 4 dietary treatments. The primary outcome variable will be change in total body weight from baseline to 2 years. Secondary outcomes related to obesity are body fat, BMI, waist circumference, visceral fat, and hepatic and skeletal muscle fat. Other outcomes are psychological factors (diet satisfaction, satiety, food craving, dietary restraint, disinhibition and hunger, and quality of life); major cardiovascular risk factors (blood pressure, low density lipoprotein [LDL] cholesterol, high density lipoprotein [HDL] cholesterol, and triglycerides); prevalence of the metabolic syndrome; blood glucose, insulin, and hemoglobin A1C; emerging cardiovascular risk factors (apolipoprotein B, VLDL and LDL particles with apolipoprotein C-III, lipoprotein[a]); microalbuminuria; and bone mineral content. The primary results will be straightforwardly applicable to public health and clinical guidelines for obesity and will increase our understanding of the biology of obesity and weight loss. The study is only accepting participants in the Boston, Massachusetts or Baton Rouge, Louisiana area. For Boston participants, contact: 617-998-1047 or www.poundslost.org. For Baton Rouge participants, contact: schoensj@pbrc.edu or 225-763-2623.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Heart Diseases, Obesity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Enrollment
811 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Four Diets Differing in Macronutrient Composition
Intervention Type
Behavioral
Intervention Name(s)
Diets Low in Saturated Fat
Primary Outcome Measure Information:
Title
Change in body weight (measured at Year 2)
Secondary Outcome Measure Information:
Title
Body fat
Title
BMI
Title
Waist circumference
Title
Visceral fat
Title
Hepatic and skeletal muscle
Title
Psychological factors from diet
Title
Major cardiovascular risk factors
Title
Prevalence of the metabolic syndrome (measured at Year 2)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Only accepting participants in the Boston, Massachusetts or Baton Rouge, Louisiana area Between the ages of 30 - 70 Willing to modify eating pattern according to instructions Overweight or obese and in good health with a BMI of 25-40 Committed to a long-term weight loss and maintenance program Willing to attend multiple weight loss group sessions Willing to increase activity level Exclusion Criteria: Pregnant, planning to become pregnant, or are breastfeeding Unwilling to participate in the schedule of group sessions and individual visits Unstable or recent onset of heart disease or any other serious illness Cannot change diet due to medical or other reasons Planning to leave the area prior to the anticipated end of participation Current participation in another clinical trial with an intervention that affects weight change Have diabetes that is treated with insulin or hypoglycemic oral medicines Diagnosis of psychiatric or emotional problems within 6 months of study Currently have an eating disorder Have hypothyroidism Have an unstable weight
Facility Information:
Facility Name
Pennington Biomedical Reseach Center, Louisiana State University
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70808
Country
United States
Facility Name
Harvard University School of Public Health
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

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Preventing Obesity Using Novel Dietary Strategies

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