Institute of Sport Science and Innovations
Kaunas, Lithuania
NCT Number: NCT06147557
The goal of this prospective interventional study is to examine if repeated brief hot stimuli affects glucose metabolism and substrate oxidation in young non-obese adults. Young adult participants were asked to participate in fourteen 5-min procedures involving whole body passive heating at 45°C water.
The main question it aims to answer is: "Does repeated brief noxious heat stimuli is sufficient to improve glucose tolerance, insulin sensitivity, and fat oxidation in young non-obese adults?"
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Notify Me18 year–35 year
All sexes
Interventional
Not applicable
Kaunas, Lithuania
No studies yet addressed whether brief heat stimuli could be viable time-efficient alternative approach in order to improve glucose metabolism and fat oxidation. Consequently, we aimed to examine the ability of brief noxious heat stimuli to improve glucose tolerance, insulin sensitivity, and fat oxidation in young adults. Non-obese males and females completed fourteen 5-min sessions involving whole body passive heating at 45°C water. Changes in catecholamines, cytokines, substrate oxidation, resting energy expenditure, glucose tolerance and insulin response were assessed.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
14 heat sessions, during each session subjects were fully immersed in a 45°C water bath for 5 minutes.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
The venous plasma adrenaline and noradrenaline concentrations (in ng/mL) were measured using enzyme-linked immunosorbent assay kits and a Spark multimode microplate reader
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
The venous serum interleukin-6 and tumor necrosis factor alpha concentrations (in pg/mL) were measured using enzyme-linked immunosorbent assay kits and a Spark multimode microplate reader
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
The venous glucose concentration (in mmol/L) was measured using a Glucocard X-mini plus meter.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
The venous serum insulin concentrations (in μIU/mL) were measured using enzyme-linked immunosorbent assay kits (Cat. No. E-EL-H2237, Elabscience, China) and a Spark multimode microplate reader (Tecan, Austria).
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Indices for insulin sensitivity/resistance assessment were computed using the homeostatic model assessment for insulin resistance, quantitative insulin-sensitivity check index (QUICKI), and the Matsuda insulin sensitivity index were calculated.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Oxygen consumption (VO2) and carbon dioxide (VCO2) output on a breath-by breath basis using a stationary MetaLyzer® 3B spiroergometry system (Cortex Biophysik GmbH) was measured at rest, and the respiratory quotient (RQ=VCO2/VO2) was computed to determine substrate utilisation.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Oxygen consumption (VO2) and carbon dioxide (VCO2) output on a breath-by breath basis using a stationary MetaLyzer® 3B spiroergometry system (Cortex Biophysik GmbH) was measured at rest, and the fat oxidation (FATox; g/min) was calculated by using the equation: FATox = 1.67 × VO2 - 1.67 × VCO2,
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Oxygen consumption (VO2) and carbon dioxide (VCO2) output on a breath-by breath basis using a stationary MetaLyzer® 3B spiroergometry system (Cortex Biophysik GmbH) was measured at rest, and the carbohydrate oxidation (CARBox; g/min) was calculated by using the equation: CARBox = 4.55 × VCO2 - 3.21 × VO2
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Oxygen consumption (VO2) and carbon dioxide (VCO2) output on a breath-by breath basis using a stationary MetaLyzer® 3B spiroergometry system (Cortex Biophysik GmbH) was measured at rest, and the resting energy expenditure (REE; kcal/day) was calculated by using the Weir equation: REE = (3.941(VO2) + 1.106(VCO2)) × 1440.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Body mass (in kg) was evaluated using Tanita Body Composition Analyzer.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Fat mass (in kg) was evaluated using Tanita Body Composition Analyzer.
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Fat mass (in %) was evaluated using Tanita Body Composition Analyzer
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Fat free mass (in kg) was evaluated using Tanita Body Composition Analyzer
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Fat free mass (in %) was evaluated using Tanita Body Composition Analyzer
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Body mass index (in kg/m2) was evaluated using Tanita Body Composition Analyzer
Time frame: Pre-condition, post-condition (after 14 days), and after 1 month recovery
Oxygen consumption and carbon dioxide output (in mL/min) on a breath-by breath basis using a stationary MetaLyzer® 3B spiroergometry system (Cortex Biophysik GmbH) was measured at rest.
Lithuanian Sports University
Other
Effect of Repeated Brief Passive Heat Therapy on Metabolism in Healthy Young Adults
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