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CompletedNCT00908765Updated Jan 3, 2013

Effects of Aerobe Interval Training and Moderate Continuous Training in Chronic Obstructive Pulmonary Disease Patients

An interventional study of Exercise in COPD and Chronic Obstructive Pulmonary Disease, sponsored by Norwegian University of Science and Technology. Completed at 1 site in Norway. Open to participants aged 45 Years to 80 Years. Per ClinicalTrials.gov, last updated 2013-01-03.

Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
45 Years to 80 Years
Sex
All
01

Study summary

Reduced exercise tolerance is one of the hallmarks of COPD. The principal causes for exercise intolerance are ventilatory limitation leading to deconditioning and inactivity. So far it is poorly understood which form of exercise is the most effective in training this condition. The investigators want to study the physiological response to two different training programs (High intensity aerobe interval training and moderate continuous aerobe training)with special focus on cardiac and skeletal muscle adaptions

Read the detailed description

Reduced exercise tolerance is one of the hallmarks of COPD and The principal causes for exercise intolerance are ventilatory limitation leading to deconditioning and inactivity. However the weak correlation between exercise capacity and FEV1 implies that other factors than reduced pulmonary function contributes to this impairment . Several studies have found changes in skeletal muscle, with fibre shift, increased oxidative stress, increased inflammatory cytokines and impaired mitochondrial function, suggesting a lower limb dysfunction

Numerous exercise studies in COPD patients have shown physiological and physiological benefits of training and endurance training is now regarded as an important part in pulmonary rehabilitation. It is still uncertain what type of endurance training that is most favourable for COPD patients.

In patients with heart failure and metabolic syndrome aerobe interval exercise have be shown to be superior in improving aerobic capacity and cardiac function

We therefore want conduct a study comparing training effects in patients with moderate to severe COPD, that participated in an identical training program that in HF and metabolic syndrome patients gave significant improvement in aerobic capacity, cardiac function and skeletal muscle function.

Patients will therefore be assigned to either 4x4 minutes high intensity interval treadmill exercise or continuous moderate intensity treadmill exercise 3 times pr week for 12 weeks. Aerobic capacity and work economy, pulmonary,cardiac and skeletal muscle function before and after the exercise training will be measured.

02

Conditions studied

  • COPD
  • Chronic Obstructive Pulmonary Disease

Keywords

  • Exercise Training COPD
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 20 is below the median of 72 across 2,118 interventional studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 487 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • COPD with FEV1 25-60 % of exp , FEV1%FVC\<70 %. Age 45-80 years

Exclusion criteria

Exclusion Criteria:

  • Heart failure
  • symptomatic coronary artery disease
  • cancer
  • alcohol and drug abuse
  • severe mental illness
  • Lower respiratory infection last 4 weeks
  • participation in exercise- or lung rehabilitation program last 3 months.
  • oral steroid use
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Active comparator
    Aerobe Interval Training

    High aerobic intensity treadmill walking. 4 by 4 minutes interval training on a graded treadmill at a heart rate corresponding to 85-95% of maximal heart rate. 3 times per week for 10 weeks.

    Behavioral: Exercise

  • Active comparator
    Moderate Continous Training

    Moderate continuous intensity treadmill walking on a graded treadmill at a heart rate corresponding to 60-70 of maximal heart rate, 3 times per week for 10 weeks

    Behavioral: Exercise

Interventions

  • BehavioralExercise

    1. High aerobic intensity treadmill walking. 4 by 4 minutes interval training on a graded treadmill at a heart rate corresponding to 85-95% of maximal heart rate. 3 times per week for 10 weeks. 2. Moderate continuous intensity treadmill walking on a graded treadmill at a heart rate corresponding to 60-70 of maximal heart rate, 3 times per week for 10 weeks

    Also known as: non

06

What researchers measure

Primary outcomes

  1. VO2-peak

    Time frame: At inclusion and after 12 weeks of exercise training

Secondary outcomes

  1. Cardiac function

    Time frame: At inclusion and after 12 weeks of exercise training

  2. Skeletal muscle function

    Time frame: At inclusion and after 12 weeks of exercise training

07

Study locations

1 site
  • Department of Circulation and Medical Imaging , NTNU
    Trondheim, 7089, Norway
08

References and documents

Publications

  • Bronstad E, Tjonna AE, Rognmo O, Dalen H, Heggli AM, Wisloff U, Ingul CB, Steinshamn S. Aerobic exercise training improves right- and left ventricular systolic function in patients with COPD. COPD. 2013 Jun;10(3):300-6. doi: 10.3109/15412555.2012.745843. Epub 2012 Dec 28. PubMed 23272664 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 3, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00908765
Lead sponsor
Norwegian University of Science and Technology
Responsible party
Sponsor
First posted
May 27, 2009
Start date
Aug 2008
Primary completion
Dec 2008
Completion
Sep 2009
Last update
Jan 3, 2013

Study contacts

Sigurd Steinshamn, MD PhD
principal investigator · NTNU , Trondheim
Eivind Brønstad, MD
principal investigator · NTNU, Trondheim

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.

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