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Effect of High Altitude Exposure, Acclimatization and Re-exposure on Postural Control in Lowlanders

Effect of High Altitude Exposure, Acclimatization and Re-exposure on Postural Control in Lowlanders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02730182
Enrollment
21
Registered
2016-04-06
Start date
2016-04-09
Completion date
2016-05-04
Last updated
2019-01-17

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

postural control, high altitude

Brief summary

Prospective interventional trial in lowlanders evaluating the effect of acute exposure, acclimatization and re-exposure to high altitude on postural control

Detailed description

Baseline measurements including the assessment of the center of pressure during 30s, the cerebral oxygen saturation and a sharpened Romberg test will be performed in Santiago de Chile, 520 m, over the course of 3 days. Participants will then travel by commercial airline (5 h flight) and by bus (3 h ride) to the base camp of the Atacama Large Millimeter/Submillimeter Array (ALMA) telescope station located at 2900 m near San Pedro de Atacama, northern Chile. Participants will stay there for the next 8 nights and they will be spend the days (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 8 day altitude sojourn participants will return to the Santiago area (520 m) for a 6 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
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* born, raised and currently living \<800m * No overnight stay at altitudes \>1500 m 4 weeks before the study

Exclusion criteria

* Previous altitude intolerance to altitude \<3000 m * Pregnancy * Health impairment, which requires regular treatment

Design outcomes

Primary

MeasureTime frameDescription
Center of pressure path length measured by Wii-balance boardLow altitude sojourn at 520 m; first sojourn at 5050 m Day 2, 7; second sojourn at 5050 m Day 2, 7Changes in center of pressure path length during the 2 sojourns at 5050 m and compared to lowland.

Secondary

MeasureTime frameDescription
Postural stability measured by sharpened Romberg-test and heel-to-toe walkLow altitude sojourn at 520 m; first sojourn at 5050 m Day 2, 7; second sojourn at 5050 m Day 2, 7Changes in postural stability during the 2 sojourns at 5050 m and compared to lowland.
Cerebral tissue oxygen saturation measured by near infrared spectroscopyLow altitude sojourn at 520 m; first sojourn at 5050 m Day 2, 7; second sojourn at 5050 m Day 2, 7Changes in cerebral oxygen saturation during the 2 sojourns at 5050 m and compared to lowland.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026