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Effectiveness of Atkins Diet for Weight Loss

This study is ongoing, but not recruiting participants.

Sponsored by: National Center for Research Resources (NCRR)
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00006193
  Purpose

Dr. Atkins' New Diet Revolution has sold over 10 million copies and has been on the New York Times best seller list for 158 weeks. This and other low-carbohydrate diets, such as the ZONE, Sugar Busters, and the Carbohydrate Addicts Diet, have attracted much popular attention but little scientific evaluation. Given the widespread use of these diets, it seems prudent to evaluate them both for safety and efficacy. Therefore, the purpose of the study is to compare the effectiveness of two different weight control programs over the course of 52 weeks. These two programs are 1) the Atkins' New Diet Revolution, a low-carbohydrate, high-protein diet, and 2) Brownell's LEARN Program, a high carbohydrate, low fat diet based on behavior modification. Specifically, this study will compare short-term changes in weight, food intake, blood chemistries and mood in adult males (n=10) and females (n=10) who are randomized to either the Atkins' Diet or the LEARN Program for a period of one year. During this year, they will be under medical supervision. We will examine the effect of the two weight loss plans on changes in lipids, blood pressure, insulin sensitivity and ketones, and eating behavior. This is a feasibility study and thus the data will ultimately be used to design a large randomized trial with adequate statistical power.


Condition Intervention
Obesity
Behavioral: diet

MedlinePlus related topics:   Obesity    Weight Control   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized
  Eligibility
Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

- BMI 25-40 kg/m2 inclusive

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00006193

Locations
United States, Missouri
Washington University    
      St. Louis, Missouri, United States, 63110

Sponsors and Collaborators
  More Information


Study ID Numbers:   NCRR-M01RR00036-0761, M01RR00036
First Received:   September 7, 2000
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00006193
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Body Weight
Signs and Symptoms
Obesity
Weight Loss
Nutrition Disorders
Overweight
Overnutrition

ClinicalTrials.gov processed this record on November 20, 2008




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