The Effects of Exercise on Appetite Regulation in Overweight/Obese Individuals
Primary Purpose
Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise
Diet
Sponsored by
About this trial
This is an interventional basic science trial for Obesity
Eligibility Criteria
Inclusion Criteria:
- all ethnic groups and both genders;
- age: 21-45 yrs;
- BMI: 27-35;
- weight stable within +/- 5 percent in the last 6 months;
- sedentary (less than 1 hour of planned physical activity by self-report).
Exclusion Criteria:
- history of cardiovascular disease (CVD), diabetes mellitus, uncontrolled hypertension, untreated thyroid disease, renal disease, hepatic disease, or any other medical condition affecting weight or energy metabolism;
- unable to effectively exercise due to cardiac, pulmonary, neurologic or orthopedic reasons;
- unable to pass screening graded exercise treadmill test;
- currently smoking;
- medications affecting weight, Energy Intake (EI) or Energy Expenditure (EE) in the last 6 months;
- weight loss or weight gain of >5 percent in past 6 months;
- currently pregnant, lactating or less than 6 months post-partum;
- bariatric surgery;
- major psychiatric disorder, presence of alcohol or substance abuse, current depression by history and/or a score >21 on the he Center for Epidemiologic Studies Depression Scale (CES-D), history of eating disorders and/or a score of >20 on the EATS-26;
- contraindication to MRI
Sites / Locations
- Univeristy of Colorado
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Physical Intervention
Nutritional Intervention
Arm Description
A supervised exercise program
A supervised diet program
Outcomes
Primary Outcome Measures
fMRI Response to Visual Food Cues
The neuronal response will be assessed by functional magnetic resonance imaging (fMRI) in response to visual food cues
Blood oxygen dependent signal (BOLD) response in exposure to visual food cues will be measured during a fMRI scan and the difference between responses in those who lose weight vs. those who do not lose weight will be compared.
Secondary Outcome Measures
Full Information
NCT ID
NCT02047721
First Posted
January 15, 2014
Last Updated
October 20, 2020
Sponsor
University of Colorado, Denver
Collaborators
American Diabetes Association
1. Study Identification
Unique Protocol Identification Number
NCT02047721
Brief Title
The Effects of Exercise on Appetite Regulation in Overweight/Obese Individuals
Official Title
The Effects of Exercise on Appetite Regulation in Overweight/Obese Individuals
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
June 19, 2019 (Actual)
Study Completion Date
June 19, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
American Diabetes Association
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In this study the Investigators are examining the effects of a 12-week exercise program (intervention) on measures of appetite and food intake regulation in overweight to mildly obese healthy adults. The Investigators hypothesize that individuals who lose a significant amount of weight in response to the intervention will show a reduction in the brain response to food cues as measured by functional magnetic resonance imaging (fMRI) when compared to those who do not lose weight. These changes in neuronal activity will be associated to physiologic and behavioral measures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
69 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Physical Intervention
Arm Type
Experimental
Arm Description
A supervised exercise program
Arm Title
Nutritional Intervention
Arm Type
Experimental
Arm Description
A supervised diet program
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
The intervention gradually increases EE from 150-200 kcal/day 5 days per week to a target of 400 kcal/d 5 days per week and will last a total of 12 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Diet
Intervention Description
A supervised diet program which has been successfully implemented by our group with a goal being to reduce energy intake by ~2000 kcal/week.
Primary Outcome Measure Information:
Title
fMRI Response to Visual Food Cues
Description
The neuronal response will be assessed by functional magnetic resonance imaging (fMRI) in response to visual food cues
Blood oxygen dependent signal (BOLD) response in exposure to visual food cues will be measured during a fMRI scan and the difference between responses in those who lose weight vs. those who do not lose weight will be compared.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
all ethnic groups and both genders;
age: 21-45 yrs;
BMI: 27-35;
weight stable within +/- 5 percent in the last 6 months;
sedentary (less than 1 hour of planned physical activity by self-report).
Exclusion Criteria:
history of cardiovascular disease (CVD), diabetes mellitus, uncontrolled hypertension, untreated thyroid disease, renal disease, hepatic disease, or any other medical condition affecting weight or energy metabolism;
unable to effectively exercise due to cardiac, pulmonary, neurologic or orthopedic reasons;
unable to pass screening graded exercise treadmill test;
currently smoking;
medications affecting weight, Energy Intake (EI) or Energy Expenditure (EE) in the last 6 months;
weight loss or weight gain of >5 percent in past 6 months;
currently pregnant, lactating or less than 6 months post-partum;
bariatric surgery;
major psychiatric disorder, presence of alcohol or substance abuse, current depression by history and/or a score >21 on the he Center for Epidemiologic Studies Depression Scale (CES-D), history of eating disorders and/or a score of >20 on the EATS-26;
contraindication to MRI
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristina Legget, PhD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
Univeristy of Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Effects of Exercise on Appetite Regulation in Overweight/Obese Individuals
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