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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05584527
Other study ID # 2021PBMD08
Secondary ID 2022-A01862-41
Status Recruiting
Phase
First received
Last updated
Start date November 28, 2022
Est. completion date May 2025

Study information

Verified date December 2022
Source Direction Centrale du Service de Santé des Armées
Contact Keyne CHARLOT, PhD
Phone 178651303
Email keyne.charlot@intradef.gouv.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Military personnel and athletes have a very high energy expenditure which is increased during certain key periods (intense training, competition and mission). Compensating for this expenditure through food can be complicated by physiological ingestive limits and logistical and organizational constraints (number of meals, availability of food), which leads these populations to regularly experience energy deficit situations (intake below requirements), which could alter physical and cognitive performance and major physiological functions. Among the many constraints to which military personnel and athletes are exposed to (stress, sleep deprivation, travel, etc.) that can increase the risk of energy deficits, the impact of thermal environmental constraints is not well known. The seasonal impact and travel to countries with very different thermal environments can lead these populations to experience cold and hot conditions for long periods. Understanding how heat and cold exposure modifies appetite and energy intake therefore appears to be of great importance. The hypothesis of this study is that a 24 h heat exposure would produce a rapid and long-lasting anorexigenic action impacting energy intake, while a cold exposure would produce the opposite effect (orexigenic action).


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date May 2025
Est. primary completion date May 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Male - Aged 18 to 40 years old - Active (= 3 hours of physical activity per week) - Healthy (no metabolic pathology) - Affiliated to the social security system - Having given written consent to participate. Exclusion Criteria: - Unusual eating pattern (< 3 meals per day) or irregular eating pattern - Pattern of dietary restriction (determined by the Three-Factor Eating Questionnaire-21) - Unusual sleep pattern (Epworth score > 10, insomnia severity score > 14, Pittsburgh Sleep Quality Index > 5), sleep duration < 6 h per night or difficulty falling asleep) - Metabolic pathology - On medication - Previously exposed to unusual levels of heat or cold (vacation, missions) in the 4 months prior to inclusion - Refusal to participate.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Heat exposure (32°C)
The participants will be exposed to heat (32°C) for 24 hours in a climatic apartment. During the exposure, food intake and energy expenditure will be measured several physiological tests will be performed: hunger and thirst questionnaires, thermal sensations, skin temperature measurement, weighing, olfactory and gustatory capacities, food preference questionnaire, etc. sleep brain activity will be monitored using a headband urine and saliva samples will be collected.
Cold exposure (16°C)
The participants will be exposed to cold (16°C) for 24 hours in a climatic apartment. During the exposure, food intake and energy expenditure will be measured several physiological tests will be performed: hunger and thirst questionnaires, thermal sensations, skin temperature measurement, weighing, olfactory and gustatory capacities, food preference questionnaire, etc. sleep brain activity will be monitored using a headband urine and saliva samples will be collected.
Thermoneutral exposure (24°C)
The participants will be exposed to a thermoneutral environment (24°C) for 24 hours in a climatic apartment. During the exposure, food intake and energy expenditure will be measured several physiological tests will be performed: hunger and thirst questionnaires, thermal sensations, skin temperature measurement, weighing, olfactory and gustatory capacities, food preference questionnaire, etc. sleep brain activity will be monitored using a headband urine and saliva samples will be collected.

Locations

Country Name City State
France Institut de Recherche Biomédicale des Armées Brétigny-sur-Orge

Sponsors (1)

Lead Sponsor Collaborator
Direction Centrale du Service de Santé des Armées

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total energy intake (in kilojoules) measured at the end of each condition (heat exposure, cold exposure and thermoneutral exposure) Through study completion (30 months)
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