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CompletedNCT04075565HypoxiaUpdated Feb 19, 2026Results posted

The Psychophysiological Effect of Simulated and Terrestrial Altitude

An interventional study of Terrestrial altitude and Cloud 9 in Hypoxia, Altitude Hypoxia and Altitude Sickness, sponsored by University of Applied Sciences and Arts of Southern Switzerland. Completed at 3 sites in Switzerland. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-19.

Sponsored by University of Applied Sciences and Arts of Southern Switzerland · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

The aim of this study is to compare the psychophysiological effects of terrestrial altitude with a normobaric, hypoxic situation.

Read the 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.

02

Conditions studied

  • Hypoxia
  • Altitude Hypoxia
  • Altitude Sickness
  • Altitude
  • Mountain Sickness
  • Hypoxia, Altitude

Keywords

  • hypoxia
  • altitude
  • physiology
  • cognition
03

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Investigator)
Enrollment
20 participants (actual)

Study arms

  • Active comparator
    Simulated altitude

    The participants are exposed to simulated altitude in a normobaric situation.

    Behavioral: Cloud 9

  • Experimental
    Terrestrial altitude

    The participants are exposed to terrestrial altitude in a hypobaric situation.

    Behavioral: Terrestrial altitude

  • No intervention
    Control

    the participants are exposed to a normoxic and normobaric environment.

Interventions

  • BehavioralTerrestrial altitude

    Terrestrial altitude: The volunteers are in an SAC hut at an altitude of 3000 m. By means of this exposure the psychophysiological effect under hypobaric and hypoxic conditions is determined. The subjects spend the night in this SAC hut and the measurements are repeated the next day.

  • BehavioralCloud 9

    Cloud 9 is a solid, certified product that complies with European Directives on Electromagnetic Compatibility, Machine Directive, Air Pressure Equipment and Low Voltage Equipment (89/336 / EEC, 91/368 / CEE, 93/68 / CEE, 97/23 / EC, EN61010-1 All directives are in writing in the Supplements to this Ethics Application. Simulated height: The subjects are in the laboratory of our institution and are connected to the Cloud 9 by means of a mask. Subjects are exposed to a simulated altitude of 3530m under normobaric conditions. By means of this intervention the psychophysiological effect under normobaric and hypoxic conditions is determined.

05

What researchers measure

Primary outcomes

  1. Oxygenation of the Brain

    Brain oxygen saturation is measured non-invasively using a deep tissue oxygenation monitor (moorVMS-NIRS, moor instruments, www.moor.co.uk). For this purpose, adhesive electrodes are applied over the muscle and the forehead. This measurement is taken during the baseline measurements, and during the cognitive performance test. This outcome measure reports the change from baseline for the oxygenation of the brain.

    Time frame: Baseline (participants seated for 15 minutes) and during the cognitive performance under normobaric hypoxia, hypobaric hypoxia, and control conditions (mean over time)

  2. Oxygenation of the Blood

    The oxygen saturation of the blood (SpO2) is measured with a portable pulse oximeter with finger clip probe (Nonin 7500, Nonin medical B.V., Plymouth, USA). This measurement is taken during the baseline measurements and after the step-up task. This outcome measure reports the change from baseline for the oxygenation of the blood.

    Time frame: Continuously during the 15-minute seated baseline period before each trial (mean over 15min) and at the end of the step-up test (point measurement)

  3. Mean Arterial Pressure

    Blood pressure was measured using an automated sphygmomanometer monitor from the left brachial artery. MAP was calculated using the following formula: MAP = diastolic blood pressure + (systolic blood pressure-diastolic blood pressure) / 3.

    Time frame: At the end of the 15-minute baseline seated period before each trial and at the end of the 3-minute submaximal step-test (Point measurements)

  4. Heart Rate

    The heart rate is measured using a pulse belt and an additional 2-point ECG (Actiheart, Camntech Ltd., Cambridge, UK). This measurement is taken during the baseline measurements and after the step-up task. This outcome measure reports the change from baseline for the heart rate.

    Time frame: at baseline and the end of the submaximal step test (point measurements)

  5. Concentration of Blood Lactate

    Lactate measurements are performed by capillary blood measurement. This measurement is taken during the baseline measurements and after the step-up task.

    Time frame: at the end of 15min baseline period and the end of the step-up test (point measurements)

  6. Sleep Quality

    Sleep quality of the night before the experimental day was assessed using the validated and reliable GSQS, consisting of a 16-item true or false questionnaire. GSQS scores ranged from 0 to 16 whereas higher scores indicated lower subjective sleep quality.

    Time frame: Before the cognitive performance test (point measurement)

  7. Altitude Sickness

    Altitude sickness is measured with "Lake Louis acute mountain sickness scale", choosing the most appropriate answer from 5 questions. Questions range from 0 (=no symptoms) to 4 (=severe symptoms). LLAMS symptoms were assessed at the end of each experimental measurement.

    Time frame: After performing the 3-min step-test (point measurment)

  8. Concentration of Salivary Cortisol

    Salivary cortisol was assessed from the n = 10 female participants to assess the daily stress level after each experimental day. Through a straw, 3mL of saliva was collected and stored in a refrigerator until the analyses were performed the next day using the enzyme-linked immunosorbent assay (ELISA) method.

    Time frame: After each experimental day, in the evening between 8:30 PM and midnight, measured once before participants went to bed (point measurment)

06

Results

Posted Feb 19, 2026

Participant flow

This is a randomised crossover trials. The same 20 participants were tested in all conditions

Participant flow — Overall Study
MilestoneExperimental: Normobaric Normoxia, Normobaric Hypoxia and Then Hypobaric Hypoxia
Started20
Normobaric normoxia20
Normobaric hypoxia20
Hypobaric hypoxia first day20
Hypobaric hypoxia after overnight20
Completed20
Not completed0

Outcome measures

PrimaryOxygenation of the Brain

Brain oxygen saturation is measured non-invasively using a deep tissue oxygenation monitor (moorVMS-NIRS, moor instruments, www.moor.co.uk). For this purpose, adhesive electrodes are applied over the muscle and the forehead. This measurement is taken during the baseline measurements, and during the cognitive performance test. This outcome measure reports the change from baseline for the oxygenation of the brain.

Time frame:
Baseline (participants seated for 15 minutes) and during the cognitive performance under normobaric hypoxia, hypobaric hypoxia, and control conditions (mean over time)
Reported as:
Median · percentage of oxygen saturation
Oxygenation of the Brain
percentage of oxygen saturationSimulated AltitudeTerrestrial AltitudeControl
rest54.6 ± 4.654.3 ± 4.959.4 ± 3.8
during congnitive performance test55.4 ± 4.555.6 ± 5.160.7 ± 3.8
PrimaryOxygenation of the Blood

The oxygen saturation of the blood (SpO2) is measured with a portable pulse oximeter with finger clip probe (Nonin 7500, Nonin medical B.V., Plymouth, USA). This measurement is taken during the baseline measurements and after the step-up task. This outcome measure reports the change from baseline for the oxygenation of the blood.

Time frame:
Continuously during the 15-minute seated baseline period before each trial (mean over 15min) and at the end of the step-up test (point measurement)
Reported as:
Mean · % SpO2
Oxygenation of the Blood
% SpO2Simulated AltitudeTerrestrial Altitude (Day 1)Terrestrial Altitude (Day 2)Control
Rest91.3 ± 1.789.5 ± 1.890.7 ± 1.895.8 ± 1.2
after 3-min step-test80.5 ± 80.578.7 ± 3.180.5 ± 3.090.7 ± 2.8
PrimaryMean Arterial Pressure

Blood pressure was measured using an automated sphygmomanometer monitor from the left brachial artery. MAP was calculated using the following formula: MAP = diastolic blood pressure + (systolic blood pressure-diastolic blood pressure) / 3.

Time frame:
At the end of the 15-minute baseline seated period before each trial and at the end of the 3-minute submaximal step-test (Point measurements)
Reported as:
Mean · mmHg
Mean Arterial Pressure
mmHgSimulated AltitudeTerrestrial Altitude (Day 1)Terrestrial Altitude (Day 2)Control
Rest93.6 ± 8.397.4 ± 8.898.1 ± 7.794.0 ± 8.1
3-min step-test114.7 ± 11.8110.6 ± 28.0122.1 ± 10.5116.8 ± 12.7
PrimaryHeart Rate

The heart rate is measured using a pulse belt and an additional 2-point ECG (Actiheart, Camntech Ltd., Cambridge, UK). This measurement is taken during the baseline measurements and after the step-up task. This outcome measure reports the change from baseline for the heart rate.

Time frame:
at baseline and the end of the submaximal step test (point measurements)
Reported as:
Mean · beats per minute
Heart Rate
beats per minuteSimulated AltitudeTerrestrial Altitude (Day 1)Terrestrial Altitude (Day 2)Control
Rest77.6 ± 10.275.0 ± 9.686.0 ± 11.271.0 ± 10.9
3-min step-test141.6 ± 10.4141.9 ± 10.6144.9 ± 5.8137.4 ± 12.9
PrimaryConcentration of Blood Lactate

Lactate measurements are performed by capillary blood measurement. This measurement is taken during the baseline measurements and after the step-up task.

Time frame:
at the end of 15min baseline period and the end of the step-up test (point measurements)
Reported as:
Mean · mmol/l
Concentration of Blood Lactate
mmol/lSimulated AltitudeTerrestrial Altitude (Day 1)Terrestrial Altitude (Day 2)Control
rest2.0 ± 0.92.4 ± 0.82.3 ± 0.81.7 ± 0.6
3-min step-test5.0 ± 1.44.9 ± 1.54.8 ± 1.64.7 ± 2.4
PrimarySleep Quality

Sleep quality of the night before the experimental day was assessed using the validated and reliable GSQS, consisting of a 16-item true or false questionnaire. GSQS scores ranged from 0 to 16 whereas higher scores indicated lower subjective sleep quality.

Time frame:
Before the cognitive performance test (point measurement)
Reported as:
Mean · score on a scale
Sleep Quality
score on a scaleSimulated AltitudeTerrestrial Altitude (Day 1)ControlTerrestrial Altitude (Day 2)
Sleep Quality5.6 ± 1.37.0 ± 1.85.5 ± 1.95.8 ± 1.6
PrimaryAltitude Sickness

Altitude sickness is measured with "Lake Louis acute mountain sickness scale", choosing the most appropriate answer from 5 questions. Questions range from 0 (=no symptoms) to 4 (=severe symptoms). LLAMS symptoms were assessed at the end of each experimental measurement.

Time frame:
After performing the 3-min step-test (point measurment)
Reported as:
Mean · score on a scale
Altitude Sickness
score on a scaleSimulated AltitudeTerrestrial Altitude (Day 1)ControlTerrestrial Altitude (Day 2)
Altitude Sickness0.6 ± 0.71.4 ± 1.30.4 ± 0.50.6 ± 0.9
PrimaryConcentration of Salivary Cortisol

Salivary cortisol was assessed from the n = 10 female participants to assess the daily stress level after each experimental day. Through a straw, 3mL of saliva was collected and stored in a refrigerator until the analyses were performed the next day using the enzyme-linked immunosorbent assay (ELISA) method.

Time frame:
After each experimental day, in the evening between 8:30 PM and midnight, measured once before participants went to bed (point measurment)
Reported as:
Mean · μg/l
Concentration of Salivary Cortisol
μg/lSimulated AltitudeTerrestrial Altitude (Day 1)Terrestrial Altitude (Day 2)Control
Concentration of Salivary Cortisol0.24 ± 0.160.31 ± 0.190.25 ± 0.120.23 ± 0.19

Adverse events

Collected over From baseline (prior to first experimental condition) through completion of the last experimental condition for each participant (approximately 3 months).. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Simulated Altitude0/20 (0%)0/20 (0%)0/20 (0%)
Terrestrial Altitude0/20 (0%)0/20 (0%)0/20 (0%)
Control0/20 (0%)0/20 (0%)0/20 (0%)

Baseline characteristics

This is a crossover design

Age, Continuous
Age, Continuous(years)Experimental: Normobaric Normoxia, Normobaric Hypoxia and Then Hypobaric Hypoxia
Females24.8 ± 5.1
Males30.3 ± 6.3
Sex: Female, Male
Sex: Female, Male(Participants)Experimental: Normobaric Normoxia, Normobaric Hypoxia and Then Hypobaric Hypoxia
Female10
Male10
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Experimental: Normobaric Normoxia, Normobaric Hypoxia and Then Hypobaric Hypoxia
07

Study locations

3 sites
  • Fachhochschule Südschweiz
    Landquart, Kanton Graubünden 7302, Switzerland
  • University of Applied Sciences and Arts of Southern Switzerland (SUPSI)
    Landquart, Kanton Graubünden 7302, Switzerland
  • Fachhochschule Südschweiz
    Landquart, 7302, Switzerland
08

References and documents

Publications

  • Hohenauer E, Freitag L, Costello JT, Williams TB, Kung T, Taube W, Herten M, Clijsen R. The effects of normobaric and hypobaric hypoxia on cognitive performance and physiological responses: A crossover study. PLoS One. 2022 Nov 10;17(11):e0277364. doi: 10.1371/journal.pone.0277364. eCollection 2022. PubMed 36355846 ↗

Study documents

  • Protocol and statistical analysis plan · May 1, 2019

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Registry details

Key details

Study ID
NCT04075565
Lead sponsor
University of Applied Sciences and Arts of Southern Switzerland
Collaborators
University of Portsmouth, Vrije Universiteit Brussel
Responsible party
Sponsor
First posted
Aug 30, 2019
Start date
Jun 24, 2019
Primary completion
Mar 31, 2021
Completion
Apr 30, 2022
Results posted
Feb 19, 2026
Last update
Feb 19, 2026

Study contacts

Ron Clijsen, PhD
principal investigator · University of Applied Sciences and Arts of Southern Switzerland (SUPSI)

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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