Relation of Obesity With Frequency of Meals (MST 0557)

Sponsor
Rockefeller University (Other)
Overall Status
Completed
CT.gov ID
NCT00229255
Collaborator
Cornell University (Other)
22
1
2
51
0.4

Study Details

Study Description

Brief Summary

The purpose of this study is to test the relationship between frequency of meals and hepatic fat content and insulin sensitivity. We, the researchers at Rockefeller University, hypothesize that low plasma insulin levels (as achieved by periods of fasting) will prevent insulin resistance and reduce hepatic lipid content. In contrast, frequent, carbohydrate-rich meals will predispose to hepatic steatosis (non-alcoholic) and insulin resistance.

This is a 6 week inpatient study.

Condition or Disease Intervention/Treatment Phase
  • Other: high frequency of meals
  • Other: twice a day meals
N/A

Detailed Description

The hypothesis will be tested by studying two groups of normal subjects who will receive a defined weight maintenance diet: one group will be given meals twice a day and other group will be given eight meals (snacks) per day. At the beginning of the study period and after 4 weeks following the specified frequency of meals, the study subjects will have their whole body insulin sensitivity and hepatic fat content measured by the euglycemic-hyperinsulinemic clamp and MRI of the liver, respectively.

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Relation of Obesity With Frequency of Meals (MST 0557)
Study Start Date :
Mar 1, 2005
Actual Primary Completion Date :
Jun 1, 2009
Actual Study Completion Date :
Jun 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: high frequency meals group

High carbohydrate diet i.e. 65% carbohydrate, 15% protein, 20% fat for 4 weeks.

Other: high frequency of meals
high carbohydrate diet i.e. 65% carbohydrate, 15% protein, 20% fat for 4 weeks.

Active Comparator: twice-a -day meals

high carbohydrate diet i.e. 65% carbohydrate, 15% protein, 20% fat for 4 weeks

Other: twice a day meals
high carbohydrate diet i.e. 65% carbohydrate, 15% protein, 20% fat for 4 weeks.

Outcome Measures

Primary Outcome Measures

  1. We will determine total body insulin sensitivity with the help of the hyperinsulinemic-euglycemic clamp. We will also assess hepatic steatosis by conducting MRI scans on our subjects. [days 8,9,11 41 and 42]

Secondary Outcome Measures

  1. Weight, waist and hip circumference, fasting glucose and insulin, serum ketones, lipids and lipoproteins including VLDL and apolipoprotien B100, liver function tests, serum adiponectin (marker for insulin resistance), and measures of hunger. [days 1-42]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Healthy individuals

  2. Age between 18-45 years

  3. Body mass index (BMI) between 18.5 - 24.9

Exclusion Criteria:
  1. Diabetes mellitus

  2. Chronic drug treatment for any medical condition like hypertension or hyperlipidemia, hyperthyroidism or taking weight control medications.

  3. Inability to give informed consent.

  4. Inability to give contact information including permanent residence or provide evidence of stable living environment for the study period.

  5. Active weight reduction of more than 7 pounds in the last 3 months.

  6. History of bleeding or blood clotting disorders.

  7. Pregnancy or breast-feeding in the women.

  8. History of anaphylaxis or anaphylactoid-like reaction as a result of food allergies.

  9. HIV or hepatitis B and C positive subjects.

  10. Subjects with hemoglobin < 8.5 gm/dl.

  11. Abnormal liver function test (ALT, AST, alkaline phosphate, LDH, GGT or total bilirubin).

  12. Serum creatinine or BUN greater than the upper limit of the normal, serum albumin less than 3.5g/dl, or proteinuria 1+ or greater.

  13. History of alcohol intake of more than 40 g/day.

  14. Contraindications to magnetic resonance imaging (MRI) including pacemakers, surgical clips, metallic implants, neuromuscular- skeletal stimulators and internal orthopedic screws or rods.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rockefeller University Hospital New York New York United States 10021

Sponsors and Collaborators

  • Rockefeller University
  • Cornell University

Investigators

  • Principal Investigator: Markus Stoffel, MD, PHD, Rockefeller University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rockefeller University
ClinicalTrials.gov Identifier:
NCT00229255
Other Study ID Numbers:
  • MST-0557
First Posted:
Sep 29, 2005
Last Update Posted:
Jun 1, 2012
Last Verified:
May 1, 2012
Keywords provided by Rockefeller University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2012