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Alternate Day Fasting, Exercise, and NAFLD

Primary Purpose

Non-Alcoholic Fatty Liver Disease, Obesity

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Alternate day fasting
Exercise
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-Alcoholic Fatty Liver Disease

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

INCLUSION CRITERIA:

  • Age between 18 to 65 years old
  • BMI between 30.0 and 59.9 kg/m2
  • NAFLD (hepatic steatosis ≥ 5% confirmed by MRI-PDFF)
  • Sedentary (<20 min, 2x/week of light activity at 3-4 metabolic equivalents (METs) for 3 mo prior to study)

EXCLUSION CRITERIA:

  • Have chronic liver disease other than NAFLD (hepatitis B or C, primary biliary cirrhosis, sclerosing cholangitis, autoimmune hepatitis, hemochromatosis, Wilson's disease, α1-antitrypsin deficiency)
  • Consume excessive amounts of alcohol women: 70 g of ethanol (5 alcoholic drinks per week) and men 140 g of ethanol (10 drinks per week) in the past 6 months)
  • Have a history of known cardiovascular, pulmonary or renal disease
  • Diagnosed T1DM or T2DM
  • Are not weight stable for 3 months prior to the beginning of study (weight gain or loss > 4 kg)
  • Are claustrophobic or have implanted metallic/electrical devices (e.g. cardiac pacemaker, neuro-stimulator)
  • Are taking drugs that induce steatosis (e.g. corticosteroids, estrogens, methotrexate, Ca channel blockers)
  • Are taking drugs that benefit NAFLD (e.g. betaine, pioglitazone, rosiglitazone, metformin, or gemifibrozil)
  • Are taking drugs that influence study outcomes (weight loss medications)
  • Are perimenopausal or have an irregular menstrual cycle (menses that does not appear every 27-32 days)
  • Are pregnant, or trying to become pregnant
  • Are smokers

Sites / Locations

  • University of Illinois Chicago

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

Alternate day fasting

Exercise

Combination alternate day fasting plus exercise

Control

Arm Description

These participants will consume 600 kcal on the "fast day" and eat ad libitum at home on alternating "feed days".

These participants will participate in a supervised aerobic exercise program 5 times per week, 40-60 min per session, 60-85% HRmax.

These participants will consume 600 kcal on the "fast day" and eat ad libitum at home on alternating "feed days". They will also participate in a supervised aerobic exercise program 5 times per week, 40-60 min per session, 60-85% HRmax.

Controls will be instructed to maintain their weight throughout the trial, and not to change eating or physical activity habits.

Outcomes

Primary Outcome Measures

Change in hepatic steatosis
Hepatic steatosis will be measured by magnetic resonance imaging (MRI-PDFF)

Secondary Outcome Measures

Change in body weight
Measured by digital scale
Change in lean mass
Measured by dual-energy x-ray absorptiometry (DXA)
Change in fat mass
Measured by dual-energy x-ray absorptiometry (DXA)
Change in visceral fat mass
Measured by dual-energy x-ray absorptiometry (DXA)
Change in Alanine Aminotransferase (ALT)
Measured by a commercial lab (Medstar, Inc)
Change in Aspartate Aminotransferase (AST)
Measured by a commercial lab (Medstar, Inc)
Change in fasting glucose
Measured by a commercial lab (Medstar, Inc)
Change in fasting insulin
Measured by a commercial lab (Medstar, Inc)
Change in insulin sensitivity
Measured by Quantitative insulin sensitivity check index (QUICKI)
Change in insulin resistance
Measured by Homeostatic model assessment (HOMA)
Change in plasma lipid levels
Measured by a commercial lab (Medstar, Inc)
Change in HbA1c
Measured by a commercial lab (Medstar, Inc)
Change in blood pressure
Measured by a blood pressure cuff
Change in heart rate
Measured by a blood pressure cuff
Dietary intake
Measured by a 7-day food record
Physical activity
Measured by an activity monitor (Fitbit Alta)
Hepatokine - Fetuin-A (ng/ml)
Measured by ELISA
Hepatokine - FGF-21 (ng/ml)
Measured by ELISA
Hepatokine - Selenoprotein P (ng/ml)
Measured by ELISA
Sleep quality and duration
Measured by Pittsburgh Sleep Quality Index (PSQI). The PSQI is a 19-item self-report questionnaire that measures sleep quality in the past month, resulting in a total score of 0-21. Scores above 5 indicate poor sleep quality.
Insonmia severity
Measured by the Insomnia Severity Index (ISI). The ISI is a 7-item self-report questionnaire that rates each item by a 5-point Likert scale, resulting in a total score of 0-28. Scores are stratified into the following categories: no clinically significant insomnia (0-7); subthreshold insomnia (8-14); moderate severity insomnia (15-21); and severe insomnia (22-28).
Risk of obstructive sleep apnea
Measured using the 10-item self-report Berlin Questionnaire which estimates % occurrences of sleep apnea

Full Information

First Posted
June 28, 2019
Last Updated
February 18, 2023
Sponsor
University of Illinois at Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT04004403
Brief Title
Alternate Day Fasting, Exercise, and NAFLD
Official Title
Alternate Day Fasting Combined With Exercise for the Treatment of Non-alcoholic Fatty Liver Disease (NAFLD)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
September 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Chicago

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Approximately 65% of obese individuals have non-alcoholic fatty liver disease (NAFLD), and this condition is strongly related to the development of insulin resistance and diabetes. Innovative lifestyle strategies to treat NAFLD are critically needed. The proposed research will demonstrate that alternate day fasting (ADF) combined with exercise is an effective non-pharmacological therapy to treat NAFLD.
Detailed Description
Nonalcoholic fatty liver disease (NAFLD) is characterized by an accumulation of fat in the liver (not resulting from excessive alcohol consumption). Approximately 65% of obese individuals have NAFLD, and this condition is strongly related to the development of insulin resistance and type 2 diabetes. While certain pharmacological agents have been shown to reduce liver fat (i.e. thiazolidinediones), there is mounting concern regarding the safety and weight-gaining effects of these compounds. In light of this, recent research has focused on non-pharmacological lifestyle therapies to reduce hepatic steatosis, such as daily calorie restriction combined with aerobic exercise. Evidence from clinical trials suggest that this combination is an effective lifestyle therapy improve liver fat content and hepatic insulin sensitivity. More recently, it's been shown that intermittent fasting may produce even greater improvements in hepatic steatosis and hepatic insulin sensitivity, when compared to conventional calorie restriction. For instance, intrahepatic lipid accumulation was lower and insulin sensitivity was higher in mice fasted every other day, when compared to mice who were energy restricted every day. Moreover, data from human trials show that adults with obesity experience greater decreases in insulin and insulin resistance with intermittent fasting versus daily restriction. These findings suggest that intermittent fasting may be a more effective diet therapy to reduce hepatic steatosis and improve insulin sensitivity, when compared to daily calorie restriction. Although these findings are very promising, these data still require confirmation by a randomized controlled clinical trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Alcoholic Fatty Liver Disease, Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alternate day fasting
Arm Type
Experimental
Arm Description
These participants will consume 600 kcal on the "fast day" and eat ad libitum at home on alternating "feed days".
Arm Title
Exercise
Arm Type
Experimental
Arm Description
These participants will participate in a supervised aerobic exercise program 5 times per week, 40-60 min per session, 60-85% HRmax.
Arm Title
Combination alternate day fasting plus exercise
Arm Type
Experimental
Arm Description
These participants will consume 600 kcal on the "fast day" and eat ad libitum at home on alternating "feed days". They will also participate in a supervised aerobic exercise program 5 times per week, 40-60 min per session, 60-85% HRmax.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Controls will be instructed to maintain their weight throughout the trial, and not to change eating or physical activity habits.
Intervention Type
Other
Intervention Name(s)
Alternate day fasting
Intervention Description
The diet involves consuming 600 kcal on the "fast day" and eat ad libitum at home on alternating "feed days".
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
The exercise intervention involves supervised aerobic exercise program 5 times per week, 40-60 min per session, 60-85% HRmax.
Primary Outcome Measure Information:
Title
Change in hepatic steatosis
Description
Hepatic steatosis will be measured by magnetic resonance imaging (MRI-PDFF)
Time Frame
Change from week 1 to week 12
Secondary Outcome Measure Information:
Title
Change in body weight
Description
Measured by digital scale
Time Frame
Change from week 1 to week 12
Title
Change in lean mass
Description
Measured by dual-energy x-ray absorptiometry (DXA)
Time Frame
Change from week 1 to week 12
Title
Change in fat mass
Description
Measured by dual-energy x-ray absorptiometry (DXA)
Time Frame
Change from week 1 to week 12
Title
Change in visceral fat mass
Description
Measured by dual-energy x-ray absorptiometry (DXA)
Time Frame
Change from week 1 to week 12
Title
Change in Alanine Aminotransferase (ALT)
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in Aspartate Aminotransferase (AST)
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in fasting glucose
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in fasting insulin
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in insulin sensitivity
Description
Measured by Quantitative insulin sensitivity check index (QUICKI)
Time Frame
Change from week 1 to week 12
Title
Change in insulin resistance
Description
Measured by Homeostatic model assessment (HOMA)
Time Frame
Change from week 1 to week 12
Title
Change in plasma lipid levels
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in HbA1c
Description
Measured by a commercial lab (Medstar, Inc)
Time Frame
Change from week 1 to week 12
Title
Change in blood pressure
Description
Measured by a blood pressure cuff
Time Frame
Change from week 1 to week 12
Title
Change in heart rate
Description
Measured by a blood pressure cuff
Time Frame
Change from week 1 to week 12
Title
Dietary intake
Description
Measured by a 7-day food record
Time Frame
Change from week 1 to week 12
Title
Physical activity
Description
Measured by an activity monitor (Fitbit Alta)
Time Frame
Change from week 1 to week 12
Title
Hepatokine - Fetuin-A (ng/ml)
Description
Measured by ELISA
Time Frame
Change from week 1 to week 12
Title
Hepatokine - FGF-21 (ng/ml)
Description
Measured by ELISA
Time Frame
Change from week 1 to week 12
Title
Hepatokine - Selenoprotein P (ng/ml)
Description
Measured by ELISA
Time Frame
Change from week 1 to week 12
Title
Sleep quality and duration
Description
Measured by Pittsburgh Sleep Quality Index (PSQI). The PSQI is a 19-item self-report questionnaire that measures sleep quality in the past month, resulting in a total score of 0-21. Scores above 5 indicate poor sleep quality.
Time Frame
Change from week 1 to week 12
Title
Insonmia severity
Description
Measured by the Insomnia Severity Index (ISI). The ISI is a 7-item self-report questionnaire that rates each item by a 5-point Likert scale, resulting in a total score of 0-28. Scores are stratified into the following categories: no clinically significant insomnia (0-7); subthreshold insomnia (8-14); moderate severity insomnia (15-21); and severe insomnia (22-28).
Time Frame
Change from week 1 to week 12
Title
Risk of obstructive sleep apnea
Description
Measured using the 10-item self-report Berlin Questionnaire which estimates % occurrences of sleep apnea
Time Frame
Change from week 1 to week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
INCLUSION CRITERIA: Age between 18 to 65 years old BMI between 30.0 and 59.9 kg/m2 NAFLD (hepatic steatosis ≥ 5% confirmed by MRI-PDFF) Sedentary (<20 min, 2x/week of light activity at 3-4 metabolic equivalents (METs) for 3 mo prior to study) EXCLUSION CRITERIA: Have chronic liver disease other than NAFLD (hepatitis B or C, primary biliary cirrhosis, sclerosing cholangitis, autoimmune hepatitis, hemochromatosis, Wilson's disease, α1-antitrypsin deficiency) Consume excessive amounts of alcohol women: 70 g of ethanol (5 alcoholic drinks per week) and men 140 g of ethanol (10 drinks per week) in the past 6 months) Have a history of known cardiovascular, pulmonary or renal disease Diagnosed T1DM or T2DM Are not weight stable for 3 months prior to the beginning of study (weight gain or loss > 4 kg) Are claustrophobic or have implanted metallic/electrical devices (e.g. cardiac pacemaker, neuro-stimulator) Are taking drugs that induce steatosis (e.g. corticosteroids, estrogens, methotrexate, Ca channel blockers) Are taking drugs that benefit NAFLD (e.g. betaine, pioglitazone, rosiglitazone, metformin, or gemifibrozil) Are taking drugs that influence study outcomes (weight loss medications) Are perimenopausal or have an irregular menstrual cycle (menses that does not appear every 27-32 days) Are pregnant, or trying to become pregnant Are smokers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Krista Varady, PhD
Organizational Affiliation
University of Illinois Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Illinois Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared.

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Alternate Day Fasting, Exercise, and NAFLD

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