ClinicalTrials.Veeva

Menu

Effect of Rehabilitation at Moderate Altitude on Airway Resistance Measured With Forced Oscillation Technique in COPD-patients

E

Eastern Switzerland University of Applied Sciences

Status

Enrolling

Conditions

COPD

Treatments

Other: ambiant air
Other: Oxygen

Study type

Interventional

Funder types

Other

Identifiers

NCT07063563
inRehaExO2_FOT

Details and patient eligibility

About

Airway resistance will be measured using the forced oscillation technique (FOT). The parameters Rrs, Xrs, and ∆Xrs will be compared before and after a pulmonary rehabilitation cycle at moderate altitude. Additionally, the differences between low and moderate altitude will also be examined.

Enrollment

52 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥18 years
  • Stable clinical condition for >3 weeks (e.g., no exacerbations)
  • Resting SpO₂ ≥88% and exercise-induced hypoxemia defined as a drop in SpO₂ of ≥4% and/or a level below 90% during the 6MWT
  • Informed consent documented by signature

Exclusion criteria

  • Severe daytime resting hypoxemia (SpO₂ <88%)
  • Long-term oxygen therapy
  • Unstable clinical condition requiring adjustment of pharmacological or other treatment modalities, need for intensive care, or presence of relevant severe comorbidities
  • Inability to comply with study procedures (e.g., due to language barriers, psychological disorders, neurological or orthopedic impairments, walking disability, or inability to ride a bicycle)
  • Women who are pregnant or breastfeeding
  • Enrolment in another clinical trial involving active treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Quadruple Blind

52 participants in 3 patient groups

Normoxia
Sham Comparator group
Description:
Sham air (ambient air) (5l/min) will be applied with the oxygen concentrator EverFlo TM via nasal cannula
Treatment:
Other: ambiant air
Other: ambiant air
Hyperoxia
Active Comparator group
Description:
Standardized supplemental oxygen therapy (SSOT) at 5 L/min will be delivered using the EverFlo™ oxygen concentrator via nasal cannula during training.
Treatment:
Other: Oxygen
Hypoxia
Experimental group
Description:
This group will train at moderate altitude
Treatment:
Other: ambiant air
Other: ambiant air

Trial contacts and locations

2

Loading...

Central trial contact

Stéphanie Saxer, Dr.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems