Insulin Resistance Clinical Trial
Official title:
The Influence of Breakfast on Hormone Responses and Cognitive Performance, as Assessed by CTET in Lean and Obese Adolescent Males
Verified date | August 2023 |
Source | Albert Einstein College of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to see what effect skipping breakfast versus consuming breakfast has on cognitive performance and the hormones responsible for glucose homeostasis in lean and obese adolescent males. The subjects will be tested on their ability to maintain attention when given several tasks called continuous temporal expectancy tasks (CTET) and electrophysiological signals using electroencephalogram (EEG) will be monitored. These two study groups will be randomized to one of two orders: (A,B) or (B,A) where A = breakfast intervention and B = no breakfast. There will be a washout period of 7 days in between study visits.
Status | Completed |
Enrollment | 17 |
Est. completion date | January 1, 2019 |
Est. primary completion date | January 1, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 13 Years to 18 Years |
Eligibility | Inclusion Criteria: 1. Healthy males 2. No history of neurological or psychiatric illness, including major depressive disorder and attention deficit disorder. 3. Normal or corrected vision using the Snellen chart 4. Normal hearing 5. BMI greater than or equal to 95th percentile according to the Center for Disease Control and Prevention (CDC) growth charts 6. HbA1C less than or equal to 5.6% 7. Hemoglobin level of greater or equal to 12g/dL Exclusion Criteria: 1. History of chronic illness and chronic use of medications that affect cognitive or glucose metabolism 2. History of substance, nicotine or alcohol dependence as assessed by CRAFFT (CAR, RELAX, ALONE, FORGET, FRIENDS, TROUBLE) questionnaire 3. History of eating disorder as assessed by the SCOFF questionnaire. 4. Developmental delay 5. Hearing and vision problems as assessed by the Snellen chart 6. Previous history of bariatric surgery 7. Currently taking supplements or medications indicated for weight loss 8. Previous history of head injury associated with loss of consciousness for several minutes 9. History of Epilepsy 10. Allergy to any of the foods used for the test breakfasts The inclusion and exclusion criteria for lean subjects will be identical to that of obese subjects with the exception that the lean subjects will be less than or equal to the 85th percentile for BMI, according to CDC growth charts. |
Country | Name | City | State |
---|---|---|---|
United States | Montefiore Medical Center of Albert Einstein College of Medicine | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
Albert Einstein College of Medicine | Montefiore Medical Center, New York State Department of Health |
United States,
Jakubowicz D, Wainstein J, Ahren B, Landau Z, Bar-Dayan Y, Froy O. Fasting until noon triggers increased postprandial hyperglycemia and impaired insulin response after lunch and dinner in individuals with type 2 diabetes: a randomized clinical trial. Diabetes Care. 2015 Oct;38(10):1820-6. doi: 10.2337/dc15-0761. Epub 2015 Jul 28. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The measurement of glucose will be euglycemic during the breakfast study visit | Area under the curve of glucose from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of C-peptide will be steady during the breakfast study visit | Area under the curve of C-peptide from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of insulin will be steady during the breakfast study visit | Area under the curve of insulin from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of free fatty acids will be steady during the breakfast study visit | Area under the curve of free fatty acids from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of glucagon-like peptide will be steady during the breakfast study visit | Area under the curve of glucagon- like peptide from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of glucagon will be steady during the breakfast study visit | Area under the curve of glucagon from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient | |
Primary | The measurement of CTET will be better during the breakfast study visit | Area under the curve of CTET from time 0min to 420 min. | 0min to 420 min during both during the treatment and control visits over the one year study period. Each study visit will be conducted on 2 separate days with a washout period of at least 1 week in between the study visits for each patient |
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