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Effect of High Altitude Exposure, Acclimatization and Re-exposure on Psychomotor Performance in Lowlanders

Effect of High Altitude Exposure, Acclimatization and Re-exposure on Psychomotor Performance and Sleep Quality in Lowlanders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02731456
Enrollment
18
Registered
2016-04-07
Start date
2016-03-01
Completion date
2017-12-31
Last updated
2018-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Effect of High Altitude

Keywords

high altitude, cognition, sleep

Brief summary

Prospective interventional trial in lowlanders evaluating the effect of acute exposure, acclimatization and re-exposure to high altitude on psychomotor vigilance to measure sustained attention.

Detailed description

Baseline measurements will be performed in Santiago de Chile, 520 m, over the course of 3 days. Participants will then travel by commercial airline (2 h flight) and by bus (2 h ride) to the ALMA base camp located at 2900 m near San Pedro de Atacama, northern Chile. Participants will stay there for the next 7 nights and they will spend the days (6 total; 6-8 h daily) at the telescope station at 5050 m while undergoing testing as described above at the first and the last day at 5050m. Daily transports from 2900 to 5050 m will be by car (1 h ride, one way). After the first 7 day altitude sojourn participants will return to the Santiago area (520 m) for a 7 day recovery period. A second altitude sojourn with an identical schedule as the one described above and a final low altitude stay of 3 days will follow.

Interventions

altitude exposure

Sponsors

University of Zurich
CollaboratorOTHER
Marc Poulin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* born, raised and currently living \<1300m * No overnight stays at altitudes \>1500m 4 weeks before the study

Exclusion criteria

* previous altitude intolerance \<3000m * pregnancy * health impairment, which requires regular treatment

Design outcomes

Primary

MeasureTime frameDescription
Sustained attention measured by a visual pychomotor vigilance test (PVT)Low altitude dojourn at 520m; forst sojourn at 5050m Day 2, 7; second sojourn at 5050m Day 2, 7Change in psychomotor response speed across two cycles of altitude exposure, comparing 5050m to 520m.

Secondary

MeasureTime frame
Indices of sleep quality measured by actigraphy (total sleep time, sleep efficiency, sleep latencyLow altitude dojourn at 520m; forst sojourn at 5050m Day 2, 7; second sojourn at 5050m Day 2, 7

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026