MedPath

Acquiring and Targeting Heat Exposures Necessary for Action

Not Applicable
Recruiting
Conditions
Heat Intolerance
Heat Stress
Fatigue; Heat
Interventions
Other: Acute and Chronic Exercise-Heat Stress
Dietary Supplement: Antioxidant Berry Supplementation
Dietary Supplement: Placebo (non-juice) Supplementation
Registration Number
NCT05678738
Lead Sponsor
University of Connecticut
Brief Summary

The purpose of this research study is to better understand ways that women and men differ physiologically, cognitively, physically, and cellularly to better prescribe helpful interventions that will prevent injury and risk of conditions like exertional heat illnesses or heatstroke. The main questions this project aims to answer are:

1. What is the relative stress contributing to performance differences between women and men during intense exercise in extremely hot and humid environments in response to exertional heat stress?

2. What is the relative contribution of responses in adipose tissue, cardiovascular tissue, gut microbiota, and musculoskeletal tissue on heat tolerance in women (vs. men) to exertional heat stress?

3. What is the impact of adding an antioxidant juice consumption regime and will it assist in enhancing performance during an acute bout of exercise-heat stress before and after heat acclimation?

Subjects enrolled and approved for participation will perform:

1. a heat acclimation protocol which includes the completion of 5 days of prescribed exercise-heat exposure

2. two separate acute exercise-heat exposures for the assessment of thermotolerance and the investigation of potential enhancements in thermoregulatory performance that may occur after the completion of a 5-day heat acclimation protocol

3. a subset of subjects enrolled and approved for participation who opt in to antioxidant berry supplement consumption will either consume the active or placebo product throughout their participation.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Participants will be healthy men and women, aged 18-50 years, who speak and read the English language fluently. This is required because some of the cognitive tests test grammatical reasoning and offer directional cues recorded as audio files in English. VO2max tests will provide evidence of level of aerobic fitness required to participate in this study. The investigators will use ≥45 ml·kg-1·min-1 for male participants, ≥40 ml·kg-1·min-1 for female participants as our threshold for inclusion.
  • The target composition of our subject sample is 50% men and 50% women.
  • No difficulties with vision, hearing, or ability to read a computer screen and operate a computer keyboard and mouse.
Exclusion Criteria
  • unable to visit the laboratory on the required, consistent schedule and consecutive required days (Days 2 and 3, Days 12 and 13)
  • any contraindications to participating in exercise lasting 60-120 minutes daily during a period of 2 consecutive days, 5 days within an 8-day period, and 2 additional days (if subjects elect to participate in the entire study, all options), screening will include resting blood pressure to exclude pre-hypertensive or hypertensive participants (resting BP > 120 mmHg and 80mmHg systolic and diastolic, respectively)
  • any contraindications to exposure to exercise-heat stress (e.g., medications that affect thermoregulation, family or personal history of issues with anesthetics that indicate possible susceptibility to malignant hyperthermia, evidence of past heat intolerance)
  • tobacco use or electronic cigarettes (e-cigarettes) within the past 6 months
  • chronic illness (including diabetes, metabolic syndrome, thyroid disease, for example) or other chronic illnesses that make it unsafe for participants to participate in daily rigorous exercise in the heat
  • regular supplementation with blood thinners, including the use of aspirin
  • acute illness (e.g., influenza, head cold, gastrointestinal illness) during the week of scheduled testing
  • current positive COVID-test or infection and past COVID infection within past 6 months
  • contraindications to blood draw and if elected to be considered for participation with microdialysis and skeletal muscle biopsy procedures, contraindications to those individual procedures
  • for subjects who may not complete a DXA scan, history of claustrophobia
  • history of allergic reactions to medical tape and/or latex
  • currently participating in "non-traditional" diets including diets such as intermittent fasting, caloric restriction, highly limited consumption of large food classes (e.g., vegan)
  • consumption of antioxidant supplementation on a regular, long-term basis outside of the aronia supplementation regime for the study
  • limited decision-making ability
  • inability to participate in extended physical activity on a treadmill (i.e., standing, running, jogging, walking)
  • consumption of a non-traditional diet including diets such as intermittent fasting, caloric restriction, highly limited consumption of large food classes (e.g., vegan) (this includes individuals who are suffering with current diagnosed or undiagnosed eating disorder)
  • allergy to povidone, ethyl chloride, lidocaine, or bacitracin
  • pregnant or positive pregnancy test during DXA pre-procedures (see DXA SOP)
  • allergy to aronia berries, monkfruit, or sham juice ingredients

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exercise-Heat Stress + Placebo (Non-juice) SupplementationPlacebo (non-juice) SupplementationAll participants (male and female) will be exposed to repeated bouts of exercise-heat stress. Participants who opt-in may be randomly assigned to receive placebo (non-juice) ingredient in addition to repeated bouts of exercise-heat stress.
Acute and Chronic Exercise-Heat StressAcute and Chronic Exercise-Heat StressAll participants (male and female) will be exposed to repeated bouts of exercise-heat stress.
Exercise-Heat Stress + Antioxidant Berry SupplementationAcute and Chronic Exercise-Heat StressAll participants (male and female) will be exposed to repeated bouts of exercise-heat stress. Participants who opt-in may be randomly assigned to receive bioactive (antioxidant berry supplement) ingredient in addition to repeated bouts of exercise-heat stress.
Exercise-Heat Stress + Antioxidant Berry SupplementationAntioxidant Berry SupplementationAll participants (male and female) will be exposed to repeated bouts of exercise-heat stress. Participants who opt-in may be randomly assigned to receive bioactive (antioxidant berry supplement) ingredient in addition to repeated bouts of exercise-heat stress.
Exercise-Heat Stress + Placebo (Non-juice) SupplementationAcute and Chronic Exercise-Heat StressAll participants (male and female) will be exposed to repeated bouts of exercise-heat stress. Participants who opt-in may be randomly assigned to receive placebo (non-juice) ingredient in addition to repeated bouts of exercise-heat stress.
Primary Outcome Measures
NameTimeMethod
Change in Rectal Temperature at RestThrough study completion, an average of 14 days

Rectal thermometer will be self-inserted by participants to assess core temperature prior to exercise-heat stress bouts

Change in Mean Skin TemperatureThrough study completion, an average of 14 days

Prior to start of exercise, participants will be instrumented with iButton skin temperature sensors on the chest, shoulder, abdomen, neck, back, thigh, and calf

Change in Whole Body Sweat RateMeasured at the beginning and end of 5 90-minute exercise-heat stress bouts (heat acclimation sessions)

Difference in body weight measurement measured prior to and at the cessation of each exercise-heat stress bout

Change in Physical Performance - Anaerobic PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for anaerobic performance with the completion of a 400 meter sprint for time. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Rectal Temperature at Thermal Threshold (38.5C)Measured throughout 5 90-minute exercise-heat stress bouts (heat acclimation sessions)

Rectal thermometer will be self-inserted by participants to assess core temperature during exercise-heat stress bouts at the thermal threshold of 38.5C

Change in Cognitive Measures - Match to SampleMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of match to sample success through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Heart Rate at Thermal Threshold (38.5C)Measured throughout 5 90-minute exercise-heat stress bouts (heat acclimation sessions)

A heart rate monitor will be worn by participants throughout the exercise-heat stress bouts to assess HR at the thermal threshold of 38.5C

Change in Cognitive Measures - Visual VigilanceMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of visual vigilance through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Cognitive Measures - Four Choice TaskMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of four choice task success through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Cognitive Measures - Profile of Mood StatesMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of profile of mood states through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Cognitive Measures - Stroop TaskMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of stroop task success through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Physical Performance - Agility PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for anaerobic performance with the completion of a quick feet agility test. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Musculoskeletal Mitochondrial FunctionMeasurement completed after the performance of an exercise-heat stress bout and physical performance battery (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Musculoskeletal tissue samples will be collected for analysis of mitochondrial function

Change in Circulatory Indicators of Lipid Metabolism - NEFAsThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of lipid metabolism biomarker Non-Essential Fatty Acids (NEFAs)

Change in Circulatory Indicators of Lipid Metabolism - IGF-1Throughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of lipid metabolism biomarker Insulin Growth Factor-1 (IGF-1)

Change in Rectal Temperature Rate of RiseThrough study completion, an average of 14 days

Rectal thermometer will be self-inserted by participants to assess core temperature during exercise-heat stress bouts

Change in Heart RateThrough study completion, an average of 14 days

A heart rate monitor will be worn by participants throughout the exercise-heat stress bouts

Change in Cognitive Measures - Repeated AcquisitionMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of repeated acquisition through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Cognitive Measures - Grammatical ReasoningMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of grammatical reasoning through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Physical Performance - Balance PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for balance performance with the completion of the Balance Error Scoring System (BESS) Test. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Musculoskeletal Gene and Protein ExpressionMeasurement completed after the performance of an exercise-heat stress bout and physical performance battery (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Musculoskeletal tissue samples will be collected for analysis via RNA-seq

Change in Subcutaneous Abdominal Tissue (SCAAT) Lipolysis RateMeasurement completed after the performance of an exercise-heat stress bout and physical performance battery (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

SCAAT lipolysis rate (interstitial glycerol and ethanol output:input) will be collected and assessed for fat mobilization and subcutaneous adipose tissue blood flow during exercise-heat stress bouts

Change in Circulatory Indicators of Stress - EpinephrineThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of physiological stress biomarker Epinephrine

Change in Sweat Metabolite and Protein ExpressionMeasurement completed during each exercise-heat stress bout (Heat Tolerance Tests 1 [days 5 and 12] and 2 [days 6 and 13]) both before and immediately after heat acclimation as well as the final heat acclimation session (HA5 - day 11)

Sweat samples will be collected and assessed for metabolite and protein expression discovery via mass spectrometry

Change in Cognitive Measures - Psychomotor VigilanceMeasurement completed immediately after one exercise-heat stress bout (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participants will perform an assessment of psychomotor vigilance through a validated computer programming system. The test is part of a larger Testing battery which should take approximately 30 minutes for completion

Change in Physical Performance - Upper Body Strength PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for upper body strength performance with the completion of a handgrip strength test. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Physical Performance - Lower Body Power PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for lower body power performance with the completion of a vertical jump test. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Physical Performance - Lower Body Kinematic PerformanceMeasurements completed immediately after the cognitive battery performed during the Heat Tolerance Test 2 (days 6 and 13) both before and immediately after heat acclimation

Participants will be assessed for lower body kinematic performance with the completion of the Landing Error Scoring System (LESS) Test. This test is part of a larger physical performance battery test which should take approximately 30 minutes for completion

Change in Musculoskeletal Fiber-TypingMeasurement completed after the performance of an exercise-heat stress bout and physical performance battery (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Musculoskeletal tissue samples will be collected for fiber-type analysis via immunohistochemical procedures

Change in Resting Energy Expenditure and Macronutrient OxidationMeasurement completed after the performance of an exercise-heat stress bout and physical performance battery (Heat Tolerance Test 2 - days 6 and 13) both before and immediately after heat acclimation

Participant resting energy expenditure, fat oxidation, and carbohydrate oxidation will be assessed via indirect calorimetry for the measurement of respiratory quotient and respiratory exchange ratio

Change in Circulatory Indicators of Inflammation - IL-1BMeasurement completed during the completion of exercise-heat stress bouts (Heat Tolerance Tests 1 [days 5 and 12] and 2 [days 6 and 13]) both before and immediately after heat acclimation

Blood samples will be collected and assessed for the expression of inflammatory biomarker IL-1B

Change in Circulatory Indicators of Inflammation - IFN-gammaMeasurement completed during the completion of exercise-heat stress bouts (Heat Tolerance Tests 1 [days 5 and 12] and 2 [days 6 and 13]) both before and immediately after heat acclimation

Blood samples will be collected and assessed for the expression of inflammatory biomarker IFN-gamma

Change in Gut Microbiome DiversityMeasurement completed prior to the completion of an exercise-heat stress bout (Heat Tolerance Test 2) both before and after heat acclimation

Stool samples will be collected and assessed for the impact of gut microbiome diversity on heat intolerance

Change in Thermal SensationThrough study completion, an average of 14 days

0-8 Scale (cold to hot) that indicated how cold or hot the participant feels. 0 = extremely cold, 8 = extremely hot

Change in Circulatory Indicators of Lipid Metabolism - InsulinThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of lipid metabolism biomarker Insulin

Change in Circulatory Indicators of Stress - CortisolThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of physiological stress biomarker Cortisol

Change in Circulatory RNA ContentThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for intracellular RNA content

Change in Saliva Metabolite ExpressionMeasurement completed during each exercise-heat stress bout (Heat Tolerance Tests 1 and 2) both before and after heat acclimation as well as the final heat acclimation session (HA5)

Saliva samples will be collected and assessed for metabolite expression

Change in RecoveryThroughout study completion, an average of 14 days

Participants will be provided a WHOOP strap after the completion of their baseline visit and will be instructed on how to download the associated application and use of the device. The WHOOP device will be used to provide data on sleep quality and quantity, strain, and recovery

Change in Circulatory Indicators of Stress - NorepinephrineThroughout study completion, an average of 14 days

Blood samples will be collected and assessed for the expression of physiological stress biomarker Norepinephrine

Change in Circulatory Indicators of Inflammation - TNF-aMeasurement completed during the completion of exercise-heat stress bouts (Heat Tolerance Tests 1 [days 5 and 12] and 2 [days 6 and 13]) both before and immediately after heat acclimation

Blood samples will be collected and assessed for the expression of inflammatory biomarker TNF-a

Secondary Outcome Measures
NameTimeMethod
Change in Perception of ThirstThroughout study completion, an average of 14 days

0-9 (no thirst to extreme thirst), scale that indicates how thirsty the subject feels, a higher score is considered a negative outcome (more thirsty)

Change in Reproductive Hormone State - FSHThroughout study completion, an average of 14 days

Blood plasma samples will be collected for the measurement of circulating follicle stimulating hormone (FSH)

Change in Cardiovascular Response - Blood PressureThroughout study completion, an average of 14 days

Blood pressure will be measured manually prior to each testing session with the documentation of systolic and diastolic measurements

Change in Environmental PerceptionThroughout study completion, an average of 14 days

Scale to assess participant perception of the environmental conditions, measurement scale identified as the modified environmental symptoms questionnaire (ESQ) which includes a minimum scale of "Not at all" and a maximum scale of "Extreme". Outcomes are considered worse when associated with greater extremes in documented answers

Change in Reproductive Hormone State - LHThroughout study completion, an average of 14 days

Blood plasma samples will be collected for the measurement of circulating luteinizing hormone (LH)

Change in Perception of FatigueThroughout study completion, an average of 14 days

0-10 (no fatigue to extreme fatigue), scale indicates how fatigued the participant feels. High score indicates more fatigue (negative outcome)

Change in Rating of Perceived ExertionThroughout study completion, an average of 14 days

6-20 scale to assess participant perceived exertion levels (how hard they are working) during exercise-heat stress bouts. A greater score indicates greater levels of exertion.

Change in Sleep QualityThroughout study completion, an average of 14 days

Scale to assess participant sleep habits including quantity and quality, measurement scale identified as the Kalinska sleep diary (KSD) which is a 9-point scale with increasing severity from 1 (extremely alert) to 9 (extremely sleepy - fighting sleep)

Change in Reproductive Hormone State - EstradiolThroughout study completion, an average of 14 days

Blood plasma samples will be collected for the measurement of circulating estradiol

Change in Reproductive Hormone State - ProgesteroneThroughout study completion, an average of 14 days

Blood plasma samples will be collected for the measurement of circulating progesterone

Change in Body MassThroughout study completion, an average of 14 days

Participants will have nude body weight (kg) assessed at the beginning and end of each testing session

Change in Reproductive Hormone State - TestosteroneThroughout study completion, an average of 14 days

Blood plasma samples will be collected for the measurement of circulating testosterone

Trial Locations

Locations (1)

Human Performance Laboratory at the University of Connecticut

🇺🇸

Storrs, Connecticut, United States

© Copyright 2025. All Rights Reserved by MedPath