Brief Title
The Psychophysiological Effect of Simulated and Terrestrial Altitude
Official Title
The Psychophysiological Effect of Simulated and Terrestrial Altitude
Brief Summary
The aim of this study is to compare the psychophysiological effects of terrestrial altitude with a normobaric, hypoxic situation.
Detailed Description
Research has consistently shown that exposure to extreme environments (such as high altitude stays) may affect cognitive function. For logistical reasons and to control the experimental set-ups, most of these examinations are carried out in the laboratory. By testing under such controlled conditions, researchers can remove any co-foundational factors and isolate the cause of stress, thereby better understanding the mechanisms by which impairment can occur. However, when people are exposed to such environments in the "real world" (such as altitude), they often experience a number of other additional stressors at the same time, which can also affect their performance. Surprisingly, however, little attention has been paid to the study of these additional stressors in combination. Although the oxygen content remains constant at various altitudes (20.93%), the air pressure decreases exponentially as the altitude increases. As a result, the oxygen partial pressure in arterial blood and tissue is reduced (hypoxia), leading to a deterioration in both physical and cognitive performance. Hypoxic conditions also alter the perception of pain, which may be particularly relevant for patients suffering from hypoxic conditions. According to the authors' knowledge, there is limited literature investigating and comparing simulated and real psychophysiological responses.
Study Type
Interventional
Primary Outcome
Perfusion of the skin microcirculation
Secondary Outcome
Thermal comfort and sensation
Condition
Hypoxia
Intervention
Terrestrial altitude
Study Arms / Comparison Groups
Simulated altitude
Description: The participants are exposed to simulated altitude in a normobaric situation.
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Behavioral
Estimated Enrollment
23
Start Date
October 1, 2019
Completion Date
September 2022
Primary Completion Date
September 2021
Eligibility Criteria
Inclusion Criteria: - Healthy, adults aged 18 to 50 years - No cardiovascular disease and / or surgery - no surgery on the cardiovascular system. - No current injuries and / or pain - Regular and adequate sleep - No terrestrial altitude of 1000 m exceeded last month (including flights) - No form of hypoxia exposed last month Exclusion Criteria: - Age over 50 years - current injuries of any kind and / or pain - Acute and / or chronic pain conditions Known general diseases (e.g., diabetes mellitus) - fear of hypoxia - fear of heights or sensitivity to terrestrial altitude - Regular use of medicines (also bought by yourself), except for contraceptives - Cardiovascular diseases or abnormalities - Anomalies of the blood analysis or ECG - Psychological disorders - pregnancy / lactation
Gender
All
Ages
18 Years - 50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Contacts
, +41 81 3000 175, [email protected]
Location Countries
Switzerland
Location Countries
Switzerland
Administrative Informations
NCT ID
NCT04075565
Organization ID
2019-00504
Responsible Party
Sponsor
Study Sponsor
University of Applied Sciences and Arts of Southern Switzerland
Collaborators
University of Portsmouth
Study Sponsor
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Verification Date
May 2021