Resuscitation Clinical Trial
Official title:
Effects of Acute Hypobaric Hypoxia Exposure on Neurocognitive Performance of Pre-hospital Emergency Service Providers
The study aims to evaluate the effects of acute hypobaric hypoxia on cognitive performance
(H0: cognitive performance at 200 meters above sea level (asl) = cognitive performance at
3000 meters above sea level = cognitive performance at 5000 meters above sea level).
Before participating in the study, each participant will respond to a questionnaire related
to high altitude exposure (prior 3 months), as well as inclusion/exclusion criteria
evaluation.
On day 0, after the interview and signed informed consent, the participant will undergo a
medical examination that will include a general objective examination. Participants will
participate in a training on the emergency and safety procedures of the hypobaric hypoxia
facility, as well as a refresh on cardiopulmonary resuscitation procedure.
During the following two days (day 1 and 2) the study protocol will be executed (one test per
day). The study protocol envisages:
- a basal cognitive test battery
- blind ascent in the hypobaric chamber to simulated altitude
- cognitive test battery
- 5 minutes of recorded chest compressions on dummies
- cognitive test battery
- blind descent in the hypobaric chamber.
During the stay in the hypobaric hypoxic facility, each participant will be monitored in real
time with the Equivital© medical monitoring device.
Before and after the stay in the hypobaric hypoxic facility, a saliva sample will be
collected, and psychological tests administered.
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