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

ConditionCOPD
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEastern Switzerland University of Applied Sciences

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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)

Trial design

Design model

Sequential

Treatments tested in this trial

  • ambiant air

    Other intervention

    Standard ambiant air will be breathed during endurance training. ambiant air

  • Oxygen

    Other intervention

    SSOT and sham air (5l/min) will be applied with the oxygen concentrator EverFloTM via nasal cannula during training

  • ambiant air

    Other intervention

    Standard ambiant air will be breathed during endurance training. ambiant air

Treatment groups

52 Participants
are divided into 3 treatment groups
Group A: NormoxiaSham comparator 1 intervention
Group B: HyperoxiaActive comparator 1 intervention
Group C: HypoxiaExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

1. Change in Rrs (Respiratory System Resistance) before and after rehabilitation cycle

Rrs will be measured using the forced oscillation technique (FOT) in cmH₂O·s/L. Values will be assessed before and after the pulmonary rehabilitation cycle at moderate altitude

Time frame
baseline to 3 weeks

Secondary outcomes

1

Change in Xrs (Respiratory System Reactance) compared before and after the pulmonary rehabilitation.

Xrs will be measured using FOT in cmH₂O·s/L. Values will be compared before and after the pulmonary rehabilitation

Time frame
baseline to 3 weeks
2

Change in ∆Xrs (Difference in Reactance) before and after rehabilitation

∆Xrs will be calculated as the difference between inspiratory and expiratory Xrs values, measured in cmH₂O·s/L, before and after rehabilitation.

Time frame
baseline to 3 weeks
3

Change in Rrs, Xrs and ∆Xrs from low to moderate altitude

Time frame
From baseline at low altitude to transfer to moderate altitude at 3 days

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Eastern Switzerland University of Applied Sciences

Lead sponsor

National Center of Cardiology and Internal Medicine named after academician M.Mirrakhimov

Collaborator

University of Zurich

Collaborator