- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02296034
Blood Glucose Variability in Obese Youth Participating in a Lifestyle Modification Program
Study Overview
Status
Conditions
Detailed Description
Healthy lifestyle intervention programs aim to increase exercise and teach youth and about healthier dietary options, in hopes of avoiding obesity complications such as diabetes, and addressing the root causes of obesity. The program entitled Bright Bodies: A Lifestyle Intervention Program for Obese Youth, has been tested rigorously, showing significant improvements in body mass index and insulin resistance at both 1 and 2 years after the program and reversal of early abnormalities in glucose metabolism. While abnormalities on standardized oral glucose tolerance testing are well described in obese youth, this test may not reflect the "real life" glycemia changes in obese children. Understanding early glycemic changes in obese youth is important to better identify those at risk and strategize effective treatment plans, to avoid progression to prediabetes and diabetes. Thus the use of a continuous glucose monitor (CGM) may be a helpful adjunct to understanding the disease and therapy approaches in these patients.
A CGM is a device inserted under the skin on the abdomen which monitors glucose levels every 5 minutes, recording this information. CGM is commonly worn by kids with type 1 diabetes. The study will allow collection of information on glucose variability in much greater detail than can be seen from intermittent fingerstick glucose values or from an oral glucose tolerance test. Given the widespread epidemic of obesity and its complications, the ability to illustrate glycemic variability in obese youth is key to delineating risk categories and optimizing treatment. While lifestyle modification programs can be effective in improving measures of insulin sensitivity and OGTT results, their effect on real life glucose values has not been described. Hence the current study, aims to describe day-to-day glycemic variation in obese youth using CGM.
All enrolled subjects will wear a CGM for up to 7 days prior to initiation of the Bright Bodies program, and for up to 7 days at the end of the program. Additionally subjects will complete a food record and report exercise during both study periods. The study periods will take place during the 2 months prior to and the 2 months after completing the Bright Bodies program. The study will be explained to volunteers who meet eligibility criteria and informed consent/assent will be obtained. Demographic data will be recorded. Medical history will be obtained and a brief physical exam may be performed. Height, weight, BMI, percent body fat, fat mass, and fat free mass will be measured.
After enrollment subjects will meet with study personnel and learn how to keep a food record, with intermittent phone contact by study personnel to optimize food record compliance. They will also be asked to record exercise and any medications taken. A blinded CGM will be inserted at the beginning of each study period. Subjects will be educated regarding the CGM, including the requirement to measure blood glucose levels with a glucometer 3 times a day, at least every 12 hours (ideally on waking in the morning before eating, before dinner, and before bedtime), to calibrate the sensor. Subjects will be given a glucometer to obtain fingerstick blood sugar values and receive instruction regarding its use.
During the follow up visits the CGM will be removed, and the CGM and glucometer will be downloaded and collected. The food record will be collected.
Study Type
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Obese (BMI >95 percentile for age based on CDC growth charts)
- Willing to wear a CGM initially before and after the Bright Bodies program
- Willing to check fingersticks 3 times a day while wearing the CGM
- Willing to keep a food record before and after the Bright Bodies program
- Be in good general health without other acute or chronic illness that in the judgment of the investigator could interfere with the study or jeopardize subject safety
- Able to give consent (permission from parents and subject assent will be required)
- Female subjects of reproductive potential must be abstinent or consistently using appropriate family planning methods
Exclusion Criteria:
- Presence of any medical or psychiatric disorder that may interfere with subject safety or study conduct
- Prior participation in the Bright Bodies program.
- Diagnosis of diabetes
- Participation in a concurrent lifestyle modification (exercise/nutrition) program
- Use of any medications known to effect blood glucose levels, including oral or other systemic glucocorticoid therapy
- Subjects using herbal supplements will be excluded, due to the unknown effects of these supplements on glucose control
- Female subjects who are pregnant, lactating, or unwilling to be tested for pregnancy
- Subjects and/or parents who are not proficient in speaking/understanding the English language
- Subjects who discontinue participation in the Bright Bodies program during the study period will be excluded from follow-up monitoring
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in blood glucose pre and post meal
Time Frame: 4 months
|
Change in blood glucose from meal time to 2-4 hours afterwards, before and after Bright Bodies program
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in mean number of calories consumed
Time Frame: 4 months
|
Change in mean number of calories consumed before and after Bright Bodies program
|
4 months
|
Change in Glucose exposure
Time Frame: 4 months
|
Change in glucose exposure as measured by the area under the curve before and after Bright Bodies program
|
4 months
|
Change in food consumption breakdown
Time Frame: 4 months
|
Change in the percent of kcals from total fat, sugar, and protein of food consumed before and after Bright Bodies program
|
4 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: MIchelle Van Name, Yale University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1409014604
- K12DK094714 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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