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Clinical Trials/NCT00299273
NCT00299273TerminatedNot Applicable

Exploratory Feasibility Study: High Fat/Protein Diet in the Treatment of Obesity

Rockefeller University1 site in 1 country8 target enrollmentStarted: March 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
8
Locations
1
Primary Endpoint
Visceral adipose tissue

Study Overview

Brief Summary

The purpose of this study is to examine the effects of a low calorie high fat/protein diet on body fat and body composition in overweight and obese subjects. The investigators will also test the effects of this diet on secondary outcomes such as: fluid and electrolyte balance, cholesterol, inflammation, sugar and insulin metabolism, fat hormones, blood pressure and feelings of fullness.

Detailed Description

Participation in this study requires 2 screening visits to the outpatient clinic, and if participants qualify, 10 inpatient study weeks.

Subjects will be admitted to the Rockefeller University Hospital for the 10 week in-patient phase of the study. The first 2 weeks consist of a weight stabilization period, during which subjects will be required to eat an average American diet. This is followed by the 6 week weight loss period where subjects will be put on a low calorie high fat/protein diet. During the weight loss period, calories will be cut by 50% compared to the weight stabilization period. This will be followed by a 2 week weight maintenance period during which calories will be added to the diet to maintain the new weight. Appropriate adjustments will be made to keep the subject's weight stable.

During the entire inpatient study, subjects will consume one multivitamin per day (Centrum, always complete, from A to Zinc) and one iron supplement per day. In addition, unlimited access to zero calorie liquids (water/diet soda) will be available and subjects will be encouraged to maintain their usual activity level.

Females of reproductive age need to make sure that they do not become pregnant during the inpatient study. Urine will be tested for pregnancy once during each phase of the study.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
25 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Body mass index (BMI) of 30 to 34.9 or
  • •BMI of 25 to 29.9 and a waist circumference > 88cm (35in)
  • •Pre-menopausal-

Exclusion Criteria

  • •High Blood Pressure
  • •High Cholesterol
  • •Liver disease
  • •Kidney disease
  • •HIV positive
  • •Hepatitis B/C positive

Arms & Interventions

Low calorie high fat/protein diet

Experimental

Low calorie high fat/protein diet

Intervention: Low calorie high fat/protein diet (Behavioral)

Outcomes

Primary Outcomes

Visceral adipose tissue

Time Frame: after 6 weeks

Secondary Outcomes

  • Body composition, fluid and electrolyte balance, lipids/lipoprotein metabolism, markers of inflammation, glucose and insulin metabolism, fat hormones, blood pressure and measures of satiety.(after 6 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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