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Nutritional Restriction and Activity Thermogenesis



Nutritional Restriction and Activity Thermogenesis

For Condition: Obesity
Status: Recruiting
Sponsor(s): National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) ,
Synopsis: These studies will provide us with enormous insight regarding how obese patients adapt energetically during negative energy balance. We will gain fundamental information regarding the metabolic implications of combining food restriction with a walking program compatible to that advocated by statutory agencies. These studies will lead to improved understanding of the energetic adaptation that occurs during negative energy balance and how best to treat patients with obesity.
Details:
Eligibility:
Study Type:
  Interventional, Diagnostic, Randomized
Minimum Age/Maximum Age: 25 Years/55 Years
Genders: Both
Protocol Entry Criteria: Ninety sedentary subjects, aged 25-55, who live <10 miles from Rochester will be recruited. This age range has been selected to enable us to study individuals at the peak age-range of obesity and over-weight prevalence and to avoid issues of menopause. Subjects will not be eligible for consideration if they take two or more bouts of exercise/week or participate in sports for more than 2 hours/week. Subjects with predicted weight maintenance energy requirements of <2000 kcal/day will have been excluded at screening. This is because when we come to underfeeding by 1000 kcal/day, we want to avoid feeding any volunteer <1000 kcal/day, for safety & compliance reasons. (A) LEAN: 30 (15F,15M) lean subjects; BMI <25 kg/m2. Each lean subject will be individually matched for height (+3cm) and age (+3 years) to an obese subject so as to establish comparable groupings for body size. Subjects will have been weight-stable for six months (B) OBESE: 30 (15F,15M) obese subjects; BMI 30-35 kg/m2. Subjects will have been weight-stable for six months (C) POST-OBESE: 30 (15F,15M) patients will have had a previous BMI >30 kg/m2 and a weight loss sufficient to achieve a BMI of <26 kg/m2 maintained for at least 2 months (with weight fluctuation during this period of <1 kg) (94). We will attempt to match these subjects to the obese subjects as described above.
Total Enrollment: 90

Location and Contact Information:

Mayo Clinic *Recruiting*
Rochester,  Minnesota,  55905
United States
Recruiting James  Levine 507-255-8076


Additional Information:
Study ID Numbers:
  R01-DK 063226-01; 
Study Start Date: June 2003
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00065338

Other Obesity Studies:
1. Treatment of Binge Eating Disorder

2. The Effects of Overfeeding on Obesity-Prone (OP) and Obesity-Resistant (OR) Women

3. Prevention of weight gain

4. The use of the Internet to facilitate weight loss and maintenance.

5. Obesity Prevention in African American School Children

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