Evaluation of the Response to Hypoxia at Rest and During Exercise in a Healthy Subject After a Cryostimulation Exposure
NCT ID: NCT06174480
Last Updated: 2024-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
35 participants
INTERVENTIONAL
2024-01-25
2025-05-25
Brief Summary
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Cross-adaptations has been defined as follows: "It simply involves considering that long-term exposure (either continuous or intermittent) to a given unfavorable environment not only increases tolerance to that particular environment but also leads to gains or losses of tolerance to other unfavorable factors that the adapted organism had never encountered before." When specifically examining cross-adaptations to cold and hypoxia, only one study focusing on the human model is available. The lack of perspectives and positions regarding the results calls for further investigations.
The main objective of this study is to assess the effect of repeated exposures to cryostimulation on the variation of the respiratory exchange ratio in hypoxia during exercise.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Control Group
Participants will not undergo cryostimulation exposure but will only receive 2 1-hour hypoxia sessions at FiO2 13.5% for 1 hour, at 2-week interval
No interventions assigned to this group
Cryostimulation Group
Participants will be exposed to cryostimulation (-50°C, forced ventilation for 3 minutes) during 20 sessions over 2 weeks and will undergo 2 hypoxia sessions at FiO2 13.5% for 1 hour, at 2-week interval
Cryostimulation
Cryostimulation (-50°C, forced ventilation for 3 minutes) during 20 sessions over 2 weeks.
Interventions
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Cryostimulation
Cryostimulation (-50°C, forced ventilation for 3 minutes) during 20 sessions over 2 weeks.
Eligibility Criteria
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Inclusion Criteria
* No exposure to cryostimulation or hypoxia (FiO2 13.5%, equivalent to an altitude of 3500 m) in the last 90 days;
* No planned sports competition during the 4 weeks of the protocol;
* Maintaining a stable physical activity level (regular training, without interruption or specific competition, including sports training programs) anticipated for 4 weeks;
* No history of respiratory conditions (asthma, respiratory allergies, exercise-induced asthma, exertional dyspnea);
* Absence of any chronic medical condition;
* No ongoing medication treatments;
* Covered by a French Social Security;
* Informed consent, signed by the subject after clear and fair information about the study.
Exclusion Criteria
* Simultaneous participation in another clinical research study;
* Individuals with enhanced protection, namely minors, individuals deprived of liberty by judicial or administrative decision, persons staying in a healthcare or social facility, adults under legal protection, and finally, patients in emergency situations;
* Subject presenting a contraindication to hypoxia and/or cryostimulation.
18 Years
30 Years
MALE
Yes
Sponsors
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Poitiers University - Laboratoire MOVE UR 20296, France
UNKNOWN
Poitiers University Hospital
OTHER
Responsible Party
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Locations
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Laboratoire MOVE UR 20296 - Poitiers University
Poitiers, , France
Clinical Investigation Centre INSERM CIC1402 - Poitiers University - CHU POITIERS
Poitiers, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CRYOX
Identifier Type: -
Identifier Source: org_study_id
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