MedPath

Aerobic Interval Training in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Hypoxemia

Not Applicable
Completed
Conditions
Hypertension, Pulmonary
Pulmonary Disease, Chronic Obstructive
Hypoxia
Interventions
Other: Exercise
Registration Number
NCT03092622
Lead Sponsor
Norwegian University of Science and Technology
Brief Summary

Patients with severe Chronic Obstructive Pulmonary Disease (COPD) and low oxygen levels in the blood are at risk of developing pulmonary hypertension and strain on the right side of the heart, both of which are known to increase symptoms and worsen prognosis It is not fully established whether interval exercise training in patients with severe COPD and concomitant low oxygen levels is beneficial.

This study aims to evaluate the effects of aerobic interval exercise training in patients with severe COPD and low oxygen levels in the blood, with a particular emphasis on such effects on the cardiovascular system and pulmonary circulation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Chronic Obstructive Pulmonary Disease (COPD)
  • Forced Expiratory Volume 1 second (FEV1) <60% of predicted
  • FEV1%FVC <70 % of predicted (FVC = Forced Vital Capacity)
  • Qualify for Long term oxygen therapy (LTOT), or presence of significant desaturation on exercise.
Exclusion Criteria
  • Unstable ischaemic heart disease or valvular heart disease.
  • Active malignant disease.
  • Substance abuse.
  • Physical or mental disability that prevents participation in the exercise programme or testing.
  • Pregnancy.
  • Exacerbation of COPD or respiratory tract infection last 6 weeks before.
  • Completed pulmonary rehabilitation programme or other organised exercise programme last 3 month
  • Use of high doses of systemic steroids.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
exercise trainingExerciseOutpatients treadmill interval training, 4x4 minutes with 3 minutes in between at lower intensity. 3 sessions weekly for 10 weeks to a total of 30 sessions.
Primary Outcome Measures
NameTimeMethod
Pulmonary artery pressureChange from baseline at 10 weeks

Examined by right heart catheterisation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

St Olavs Hospital, Lungemedisinsk Avdeling & Hjertemedisinsk Avdeling

🇳🇴

Trondheim, Norway

© Copyright 2025. All Rights Reserved by MedPath