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NCT Number: NCT00771108

Exercise Dose and Nonalcoholic Fatty Liver Disease

The purpose of this research is to provide a better understanding of how exercise (walking) affects non-alcoholic fatty liver disease (NAFLD) in overweight people. NAFLD, which is common in obese people, occurs when the liver has too much fat.

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Key information

About this study

Non-alcoholic fatty liver disease (NAFLD) affects about 33% of adults in the United States. The prevalence of NAFLD is four to five times higher in obese than lean persons and is associated with insulin resistance and the metabolic syndrome. Decreasing calorie intake and increasing physical activity has been recommended as primary therapy for NAFLD, but the independent effect of aerobic exercise is unknown. The current exercise guidelines for disease prevention and weight management range from 150 min/wk, recommended by the Centers for Disease Control and the American College of Sports Medicine, to 300 min/wk, recommended by the Institute of Medicine. However, it is not known whether aerobic exercise alone can improve NAFLD, and which recommended dose of exercise might have the most beneficial effects. The purpose of this proposal is to determine the effect of moderate intensity endurance exercise on: 1) hepatic fat content; 2) hepatic lipoprotein kinetics; and 3) plasma inflammatory markers. We hypothesize that aerobic exercise will decrease hepatic fat content, improve VLDL kinetics, and decrease inflammation in a dose-dependent fashion. The results from this study will help determine exercise guidelines for obese patients with NAFLD, and lay the groundwork for future studies evaluating the effects of exercise on metabolic diseases associated with obesity.

This proposal involves conducting a randomized controlled trial that will randomize obese subjects with NAFLD (> 10% hepatic fat content) to one of two groups: Group 1 (Control, no exercise) and Group 2 (Moderate Intensity Aerobic Exercise- 150 min/wk to 300 min/wk of supervised exercise performed at 45-55% of O2 max).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-65 with Nonalcoholic Fatty Liver Disease as determined by MRS

Exclusion criteria

  • Medical History
  • Diabetes
  • Heart Disease
  • Asthma/Lung disease
  • Injury that prevents exercise
  • Social history
  • Drinking
  • More than one drink per day
  • Binge drinking on the weekends (more than 3 or 4 drinks per weekend day)
  • Smoking
  • It's OK if they were a previous smoker, but they need to have quit more than 6 months ago
  • Exercise
  • They must exercise less than one hour per week
  • Medications: must be on stable regimen of ANY medication for at least 3 months
  • Beta-Blockers
  • Lipid/cholesterol lowering medications:
  • Oral hypoglycemics (anti-diabetes medications - some like metformin are indicated for pre-diabetes)
  • Hormone replacement therapy
  • If the woman is pre-menopausal, it is OK if she is on birth control as long as she has been on it over 3 months
  • Weight history
  • Weight <300 lbs
  • BMI 30 to 45
  • Weight stable - <10lbs weight loss or gain in the last 3 months

Treatment and study plan

Exercise

Behavioral

For 16 weeks subjects will exercise from 30-60 minutes five times a week.

Other names: walking

Primary outcomes

  1. The effect of aerobic exercise on: Intrahepatic fat content

    Time frame: 3 years

Secondary outcomes

  1. VLDL-triglyceride (TG) and VLDL-Apolipoprotein B (apoB) kinetics

    Time frame: 3 years

  2. Insulin action in liver (suppression of glucose production), muscle (stimulation of glucose uptake), and adipose tissue (suppression of lipolysis).

    Time frame: 3 years

  3. Plasma markers of inflammation

    Time frame: 3 years

  4. Potential cellular mechanisms responsible for changes in insulin action and inflammation

    Time frame: 3 years

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Registry information

Acronym: ED

Important dates

Study start
2006
Primary completion
2011
Study completion
2011
First posted
Oct 13, 2008
Registry last updated
Sep 7, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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