Altitude may fog your memory for plans
NCT ID NCT07585227
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether being at a moderate altitude (like 4,000 meters) can hurt your ability to remember to do things later, called prospective memory. Fifty healthy adults will take memory tests while breathing low-oxygen air or normal air in a chamber. Researchers also want to see if breathing pure oxygen or regular air can help restore memory during low-oxygen exposure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hypoxia exposure (simulated altitude of 4,000m)
- What this could lead to
- If it works, this could help us understand how altitude affects memory, which may improve safety for pilots, climbers, or others in low-oxygen environments.
- What could go wrong
- This is a small, early-stage study in healthy volunteers, not patients. The results may not apply to real-world altitude exposure or people with health conditions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Healthy volunteer * Has provided informed consent Exclusion Criteria: * Individuals who do not understand French * Pregnant or breastfeeding women * Cardiovascular risk factor * Infectious disease within the last 4 weeks * Chronic cardiovascular, respiratory, hematological, neurological, psychiatric, or metabolic disease * History of epileptic seizures, convulsions, or loss of consciousness * Individuals with migraines * History of a bleeding disorder * History of high blood pressure * Current medication use (excluding contraception) * History of episodes of altitude intolerance * Stay at high altitude (\> 3,500 m) within the last 3 months * Anxiety score on the Hospital Anxiety and Depression (HAD) scale \> 7 * Depression score on the HAD scale \> 7 * Uncontrollable claustrophobia or a history of panic attacks
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Institut de Recherche Biomédicale des Armées
Brétigny-sur-Orge, 91220, France
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