The goal of this single-blind randomized placebo-controlled trial is to test the effects of an oral ketone supplement on appetite, cognition, metabolism, and cardiovascular function in individuals with obesity and insulin resistance. The main question\[s\] it aims to answer are: * Does taking the ketone supplement reduce appetite and improve cognition? * How does the ketone supplement alter metabolism and cardiovascular function? Participants will be asked to consume a randomly assigned ketone ester supplement or a placebo and testing will be done to see how the supplement affects the following compared to a placebo: * appetite, * cognition, * metabolism * cardiovascular function Researchers will compare individuals with obesity and insulin resistance to individuals with normal weight and no insulin resistance to see if the ketone supplement affects groups differently.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
Oral ingestion of a ketone supplement combined with a flavoring agent and diluted in water
Oral ingestion of cellulose combined with a flavoring agent and diluted in water
University of Southern Mississippi - School of Kinesiology and Nutrition
Hattiesburg, Mississippi, United States
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: Baseline (pre-ingestion)
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 30 minutes post ingestion
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 45 minutes post ingestion
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 60 minutes post ingestion
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 75 minutes post ingestion
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 90 minutes post ingestion
Blood pressure
Blood pressure responses (systolic and diastolic) to sympathoexcitation
Time frame: 105 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: Baseline (pre-ingestion)
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 30 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 45 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 60 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 75 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 90 minutes post ingestion
Heart Rate
Heart rate responses to sympathoexcitation
Time frame: 105 minutes post ingestion
Heart Rate Variability
Index of cardiac autonomic control
Time frame: Baseline (pre-ingestion)
Heart Rate Variability
Index of cardiac autonomic control
Time frame: 45 post ingestion
Cardiac Baroreflex Sensitivity
Changes in cardiac interval relative to changes in systolic blood pressure
Time frame: 105 minutes post ingestion
Hunger - Visual Digital Analog Scale (0-100)
Changes in subjective rating of hunger
Time frame: Baseline, 30, 45, 60, 75, 90, 105, 120 minutes post ingestion
Fullness - Visual Digital Analog Scale (0-100)
Changes in subjective rating of fullness
Time frame: Baseline, 30, 45, 60, 75, 90, 105, 120 minutes post ingestion
Desire to eat - Visual Digital Analog Scale (0-100)
Changes in subjective rating of desire to eat
Time frame: Baseline, 30, 45, 60, 75, 90, 105, 120 minutes post ingestion
Prospective consumption of food - Visual Digital Analog Scale (0-100)
Changes in subjective rating of prospective consumption of food
Time frame: Baseline, 30, 45, 60, 75, 90, 105, 120 minutes post ingestion
Thirst - Visual Digital Analog Scale (0-100)
Changes in subjective rating of thirst
Time frame: Baseline, 30, 45, 60, 75, 90, 105, 120 minutes post ingestion
Stroop Test - Digital Cognitive Function Test
Changes in Stroop score
Time frame: Baseline, 75 minutes
Go/No-go Test - Digital Cognitive Function Test
Changes in Go/No-go score
Time frame: Baseline, 75 minutes
Task Switching Task - Digital Cognitive Function Test
Changes in Task Switching Task score
Time frame: Baseline, 75 minutes
Number Back Test - Digital Cognitive Function Test
Changes in Number Back Test score
Time frame: Baseline, 75 minutes
Digit Span Test - Digital Cognitive Function Test
Changes in Digit Span Test score
Time frame: Baseline, 75 minutes
Prefrontal Cortex Oxygenation
Near-infrared spectroscopy
Time frame: Baseline, 90 minutes post ingestion
Peripheral Blood Flow
Doppler Ultrasound of Femoral Artery
Time frame: Baseline, 30, 60 and 90 minutes post ingestion
Peripheral Vascular Conductance
Blood flow normalized to blood pressure (mL/min/mmHg)
Time frame: Baseline, 30, 60 and 90 minutes post ingestion
Blood ketones
Ketone body level from capillary blood
Time frame: Baseline, 30, 60, 90, 120 minutes post ingestion
Blood glucose
Blood glucose level from capillary blood
Time frame: Baseline, 30, 60, 90, 120 minutes post ingestion
Oxygen Consumption from Respiratory Gases
Amount of oxygen consumed using indirect calorimetry
Time frame: Baseline and continuous for 120 minutes
Carbon Dioxide Produced from Respiratory Gases
Amount of carbon dioxide produced using indirect calorimetry
Time frame: Baseline and continuous for 120 minutes
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