8 Participants NeededMy employer runs this trial

Energy Dense Fueling for Cold Exposure

UR
Overseen ByUSARIEM Recruitment
Age: 18 - 65
Sex: Any
Trial Phase: Academic
Sponsor: United States Army Research Institute of Environmental Medicine

What You Need to Know Before You Apply

What is the purpose of this trial?

High daily energy expenditures without compensatory increases in energy intakes results in severe energy deficits during cold-weather military operations. Observational and experimental data from our laboratory suggests that consuming higher-fat, energy dense products can increase energy intake and attenuate energy deficits, however, laboratory analysis is needed to understand the impact of macronutrient manipulation on substrate oxidation and aerobic performance. This proof of concept, randomized crossover study will examine the effects of consuming an isocaloric bar (approximately 350 kcal) that is higher in carbohydrate (CHO: 50% carbohydrate, 30% fat, 20% protein) or higher in fat (FAT: 30% carbohydrate, 50% fat, 20% protein) on substrate oxidation and aerobic performance (time trial) during acute cold (5°C) exposure. Volunteers will wear shorts and a t-shirt during cold exposure, with continuous monitoring of core and skin temperatures. Baseline data will be collected on volunteer height, weight, body composition, and V̇O2peak. To ensure volunteers are familiar with exercise protocols, they will complete practice sessions of all exercise before the start of data collection. Exercise and diet will be controlled throughout data collection. 24 hours prior to data collection, volunteers will consume a lead-in study diet and will abstain from exercise. After 24 hours, volunteers will return to the laboratory for assessment of substrate oxidation and aerobic performance. Volunteers will consume the CHO or FAT treatment bars under cold conditions, followed by 60 minutes of rest prior to the start of exercise. Volunteers will then complete 90 minutes of load carriage steady-state (55 ± 5% VO2peak) treadmill exercise, wearing a ruck with weighing 30% of their total body mass. After steady-state exercise, aerobic performance will be assessed by having volunteers complete a 2-mile time trial. Indirect calorimetry will be used to determine substrate oxidation during steady-state exercise. Serial blood draws will be collected during each trial to assess circulating substrate/hormone responses. Protocol days will be separated by a minimum washout period of 6 days.

Are You a Good Fit for This Trial?

Inclusion Criteria

* Willing to refrain from alcohol, nicotine products and dietary supplement use while on study diets
My periods are regular, or I use continuous low-dose hormonal birth control.
* Only consume caffeine products while on study diets if provided by study staff
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Baseline Assessment

Baseline data collection on volunteer height, weight, body composition, and V̇O2peak. Practice sessions of all exercise protocols.

1 week
1 visit (in-person)

Treatment

Participants consume either a higher carbohydrate or higher fat isocaloric bar under cold conditions, followed by exercise protocols including steady-state treadmill exercise and a 2-mile time trial.

2 weeks
Multiple visits (in-person)

Washout Period

Minimum washout period between protocol days to prevent carryover effects.

6 days

Follow-up

Participants are monitored for safety and effectiveness after treatment.

2 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Energy Dense Fueling

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: Higher Fat Supplement BarExperimental Treatment1 Intervention
Group II: Higher Carbohydrate Supplement BarPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

United States Army Research Institute of Environmental Medicine

Lead Sponsor

Trials
67
Recruited
3,700+