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Patients With Chronic Obstructive Pulmonary Disease At Altitude

Effect of Altitude on Exercise Performance of Patients With Chronic Obstructive Lung Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01875133
Enrollment
50
Registered
2013-06-11
Start date
2013-05-31
Completion date
2013-12-31
Last updated
2015-05-19

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD)

Keywords

airway disease, bronchitis, emphysema, lung

Brief summary

The purpose of this study is to investigate the effect of a stay at moderate altitude on exercise performance of patients with chronic obstructive lung disease.

Detailed description

Patients with moderate to severe COPD living below 800 m, will be recruited to participate in a randomized cross-over field trial evaluating the hypothesis that exercise capacity during a 4 day sojourn at moderate altitude is reduced in comparison to low altitude. Outcomes will be assessed during 2 days in Zurich (490 m, low altitude baseline), 2 days at Davos Clavadel (1650 m), and 2 days at Davos Jakobshorn (2590 m). The main outcome is the 6 minute walk distance.

Interventions

stay at different altitudes: 490, 1630, 2590 m

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* chronic obstructive pulmonary disease (COPD), GOLD grade 2-3 * residents at low altitude (\<800 m)

Exclusion criteria

* Unstable condition, COPD exacerbation * Mild (GOLD 1) or very severe COPD (GOLD 4) * requirement for oxygen therapy at low altitude residence * hypoventilation * pulmonary hypertension * more than mild or unstable cardiovascular disease * use of drugs that affect respiratory center drive * internal, neurologic or psychiatric disease that interfere with protocol compliance including current heavy smoking (\>20 cigarettes per day), inability to perform 6 min walk test. * previous intolerance to moderate altitude (\<2600m). * Exposure to altitudes \>1500m for \>2 days within the last 4 weeks before the study. * Pregnant or nursing patients

Design outcomes

Primary

MeasureTime frameDescription
Change in exercise performance from baseline measured at 490 mChange in 6 min walk distance from 490 m baseline during 2 days at 2590 m6 min walk distance

Secondary

MeasureTime frameDescription
Change in exercise performance from baseline measured at 490 mChange in 6 min walk distance from 490 m baseline during 2 days at 1650 m6 min walk distance
Change in pulmonary function from baseline measured at 490 mChange in pulmonary function from 490 m baseline during 2 days at 2590 mlung volumes by spirometry
Change in arterial blood gases from baseline measured at 490 mChange in arterial blood gases from 490 m baseline during 2 days at 2590 mArterial blood gas analysis
Change in perceived exertion from baseline measured at 490 mChange in perceived exertion from 490 m baseline during 2 days at 2590 mBorg CR10 scale at end of 6 min walk

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026