How Quickly Can the Effects of Excessive Caloric Intake on Insulin Resistance be Reversed?
Primary Purpose
Obesity
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
high caloric intake
reduced caloric intake
Sponsored by
About this trial
This is an interventional other trial for Obesity focused on measuring insulin resistance, obesity, caloric intake
Eligibility Criteria
Inclusion Criteria: Healthy non-obese men and women -
Exclusion Criteria: Subjects with diabetes or a history of obesity surgery or with more than modest health problems
-
Sites / Locations
- Temple University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
high caloric intake
reduced caloric intake
Arm Description
Volunteers will receive 3 meals and 3 snacks over a 24 hour period which will contain ~ 6,000 calories. Main meals will consist of ~ 1,500 calories and snacks will contain ~ 500 calories.
On days 5 and 6 subjects will receive 3 meals only and each meal will contain ~ 333 calories for a total of 1,000/ 24 hours.
Outcomes
Primary Outcome Measures
Changes in insulin resistance
Insulin resistance will be determined by measuring changes in insulin-stimulated total body glucose uptake during euglycemic hyperinsulinemic clamping
Changes in oxidative stress
24 hour urine collections analyzed for isoprostane content
Changes in energy expenditure
Changes in energy expenditure will be assessed with a metabolic cart (indirect calorimetry)
Changes in weight
Subjects will be weighed daily
Changes in body composition
Body composition will be determined by bioelectric impedance analysis
Secondary Outcome Measures
Changes in blood glucose levels
Daily blood samples will be analyzed to determine glucose levels of glucose.
Changes in blood levels of insulin
Daily blood samples will be analyzed to determine insulin levels
Changes in blood levels of free fatty acids
Daily blood samples will be analyzed to determine free fatty acid levels
Changes in blood ketone levels
Daily blood samples will be analyzed to determine ketone levels
Changes in glucagon levels
Daily blood samples will be analyzed to determine glucagon levels
Full Information
NCT ID
NCT02505958
First Posted
July 21, 2015
Last Updated
July 25, 2022
Sponsor
Temple University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT02505958
Brief Title
How Quickly Can the Effects of Excessive Caloric Intake on Insulin Resistance be Reversed?
Official Title
How Quickly Can the Effects of Excessive Caloric Intake on Insulin Resistance be Reversed?
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 2014 (undefined)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Temple University
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Objective: To show that a 1-2 day reduction of caloric intake can reduce the insulin resistance produced by several days of overnutrition. Approach: Healthy volunteers will be admitted to the Clinical Research Center and undergo a baseline euglycemic-hyperinsulinemic clamp study to assess their insulin resistance. Subjects will then start on an overnutrition program for 4 days consisting of 3 meals and 3 snacks containing ~6,000 Kcal/24hours. A second clamp study will be performed on day 5 to demonstrate the overnutrition induced increase in insulin resistance. Starting on day 5 the subject's caloric intake will be reduced to ~1,000 Kcal for 2 days (day 5 and 6). After that on the morning of day 7, a third hyperinsulinemic-euglycemic clamp will be performed to determine whether the reduced caloric intake did reduce insulin resistance and the volunteer will be discharged from the Clinical Research Center.
Detailed Description
Study volunteers will be admitted to the Clinical Research Center at Temple University Hospital. After an overnight fast, body composition will be determined non-invasively by bioimpedance analysis (4) and a 4 h euglycemic-hyperinsulinemic clamp (using only FDA-approved regular insulin) as previously described (5) will be performed during which serum samples will be obtained for measurement of glucose, insulin, free fatty acids, ketone bodies and lipids. Oxidative stress ( 6) will be measured by 24 hour urine collections (analyzed for isoprostane content via 8-isoprostaglandin-F2alpha throughout the study period. Respiratory gas exchange rates (7) will be determined at hourly intervals (with a metabolic cart (True One, Parvo Utah) during the clamp studies and once a day on Days 2 through 6. After that, (at about 1:00 in the afternoon on Day 1) the volunteers will be started on a diet program for 4 ½ days, consisting of 3 meals and 3 snacks over a 24 hour period and containing ~ 6000 Kcal/24 h. The main meals (containing ~ 1500 Kcal/meal) will be served at ~ 8:00 in the morning (breakfast), 1:00 in the afternoon (lunch) and approximately 7:00 in the evening (dinner), the snacks (~ 500 Kcal/each) at approximately 11:00 in the morning, 4:00 in the afternoon and 11:00 in the night. On days 5 and 6, volunteers will receive 3 meals, each will contain ~333 calories. Each morning blood samples will be obtained to measure glucose insulin, free fatty acids and ketone bodies. Daily 24 h urine collections will be obtained each day. In the morning of Days 5 and 7, all procedures described for Day 1 will be repeated. In the afternoon of Day 7, the volunteers will be discharged from the hospital.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
insulin resistance, obesity, caloric intake
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
high caloric intake
Arm Type
Other
Arm Description
Volunteers will receive 3 meals and 3 snacks over a 24 hour period which will contain ~ 6,000 calories. Main meals will consist of ~ 1,500 calories and snacks will contain ~ 500 calories.
Arm Title
reduced caloric intake
Arm Type
Other
Arm Description
On days 5 and 6 subjects will receive 3 meals only and each meal will contain ~ 333 calories for a total of 1,000/ 24 hours.
Intervention Type
Other
Intervention Name(s)
high caloric intake
Intervention Description
Volunteers will be started on a diet program for 4 ½ days, consisting of 3 meals and 3 snacks over a 24 hour period and containing ~ 6000 Kcal/24 h.
Intervention Type
Other
Intervention Name(s)
reduced caloric intake
Intervention Description
On days 5 and 6, volunteers will received 3 meals (~333 calories each) totaling ~ 1,000 calories/24 hours.
Primary Outcome Measure Information:
Title
Changes in insulin resistance
Description
Insulin resistance will be determined by measuring changes in insulin-stimulated total body glucose uptake during euglycemic hyperinsulinemic clamping
Time Frame
baseline, day 4 and day 7
Title
Changes in oxidative stress
Description
24 hour urine collections analyzed for isoprostane content
Time Frame
baseline, day1, day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in energy expenditure
Description
Changes in energy expenditure will be assessed with a metabolic cart (indirect calorimetry)
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in weight
Description
Subjects will be weighed daily
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in body composition
Description
Body composition will be determined by bioelectric impedance analysis
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
Secondary Outcome Measure Information:
Title
Changes in blood glucose levels
Description
Daily blood samples will be analyzed to determine glucose levels of glucose.
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in blood levels of insulin
Description
Daily blood samples will be analyzed to determine insulin levels
Time Frame
Baseline, day1 day2, day 3, day 4, day 5, day 6, day 7
Title
Changes in blood levels of free fatty acids
Description
Daily blood samples will be analyzed to determine free fatty acid levels
Time Frame
Baseline, day1 , day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in blood ketone levels
Description
Daily blood samples will be analyzed to determine ketone levels
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
Title
Changes in glucagon levels
Description
Daily blood samples will be analyzed to determine glucagon levels
Time Frame
baseline, day 1, day 2, day 3, day 4, day 5, day 6, day 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy non-obese men and women -
Exclusion Criteria: Subjects with diabetes or a history of obesity surgery or with more than modest health problems
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ajaykumar Rao, MD
Organizational Affiliation
Temple University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Temple University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19140
Country
United States
12. IPD Sharing Statement
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How Quickly Can the Effects of Excessive Caloric Intake on Insulin Resistance be Reversed?
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