Effects of Mild Hypobaric Hypoxia on Oxygen Saturation During Sleep
NCT ID: NCT00659009
Last Updated: 2012-08-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
16 participants
INTERVENTIONAL
2008-05-31
2009-03-31
Brief Summary
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Detailed Description
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1. Replicate findings of earlier study in which no effects of altitude were observed on post sleep neurobehavioral performance, sleep quantity or quality.
2. Determine if sleep at 6000 feet has effects similar to sleep at 8000 feet.
3. Identify if central or obstructive apnea is responsible for the reduction in oxygen saturation observed during sleep at 8000 feet.
4. Determine if respiratory abnormalities observed at 6000 feet are similar but less severe than at 8000 feet.
5. Determine if there are individual differences in respiratory physiology at sea level that enable prediction of pronounced respiratory disturbances during sleep at altitude.
6. Determine if changes in autonomic nervous activity, measured by heart rate variability, occur, and if so, do they persist for 8 hours.
Twenty healthy males between 30 and 60 years of age whose baseline apnea-hypopnea index is less than 15/hour will be recruited from the general population surrounding Burnaby, British Columbia, Canada. Women are excluded because of the changes in sleep structure associated with the menstrual cycle.
Participants will be involved in the blinded crossover study for a 14 day period during which time they will monitor their sleep by actigraphy and sleep diaries, will spend 2 nights an altitude chamber at Simon Fraser University at ambient barometric pressure to become adapted to sleeping in that environment, then spend 3 study nights, each followed by 2 rest nights, sleeping at barometric pressures equivalent to sea level, 6000 feet, and 8000 feet. The order of exposures will be randomly balanced.
Pre study physiologic measures will include hypoxic ventilatory response, hypercapnic ventilatory response, and during one of the adaptation nights, apnea hypoxia index. Study sessions will consist of a 4 hour presleep period, a 6 hour sleep period, and a 1 hour post sleep period at the study barometric pressure. During the study sessions, heart rate, SpO2, polysomnographic measures, nasal air flow rates, and chest motion will be monitored and recorded. Psychomotor Vigilance Task response time will be measured before and after the sleep period. Heart rate will be recorded by ambulatory recording equipment for 8 hours following return to ambient barometric pressure conditions. This will be analyzed to determine if changes in heart rate variability are persistent.
Outcomes of primary interest will include total sleep time, duration of sleep stages, oxygen saturation, heart rate and heart rate variability, respiratory rates, air flow, and chest motion to assess if central or obstructive apnea is temporally related to reductions in oxygen saturation.
Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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1
Barometric pressure equivalent to sea level (760 mm Hg).
Sea level equivalent barometric pressure
Sleep in barometric pressure equivalent to sea level.
2
Barometric pressure equivalent to 6000 feet (609 mm Hg)
Reduced barometric pressure
Sleep in reduced barometric pressure environment.
3
Barometric pressure equivalent to 8000 feet (565 mm Hg).
Reduced barometric pressure
Sleep in reduced barometric pressure environment.
Interventions
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Reduced barometric pressure
Sleep in reduced barometric pressure environment.
Sea level equivalent barometric pressure
Sleep in barometric pressure equivalent to sea level.
Reduced barometric pressure
Sleep in reduced barometric pressure environment.
Eligibility Criteria
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Inclusion Criteria
* Between 30 and 60 years of age.
* Healthy, able to pass FAA Class III examination
* Body mass index less than 30
* Height less than 75 inches
* Ability to read and speak English
Exclusion Criteria
* Recent travel to altitudes above 5000 feet
* Use of drugs or medications that affect sleep
* History of mood or psychiatric disorders that affect sleep.
* History of medical conditions that increase risk of adverse effects of hypoxia.
* Apnea hypopnea index greater than 15/hr at ground level.
30 Years
60 Years
MALE
Yes
Sponsors
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Simon Fraser University
OTHER
Massey University
OTHER
The Boeing Company
INDUSTRY
Responsible Party
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Principal Investigators
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James M Muhm, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
The Boeing Company
Locations
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Environmental Physiology Unit, School of Kinesiology, Simon Fraser University
Burnaby, British Columbia, Canada
Countries
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Other Identifiers
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Boeing-003
Identifier Type: -
Identifier Source: org_study_id