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CompletedNCT00744484Updated Mar 7, 2022

A 12 Week Physical Training Programme for Patients With Chronic Obstructive Pulmonary Disease

An interventional study of Training in water and Training on land in Chronic Obstructive Pulmonary Disease, sponsored by Norwegian University of Science and Technology. Completed at 1 site in Norway. Open to participants aged 50 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-03-07.

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

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Feb 2008, registered Aug 2008).
Phase
Not applicable
Study type
Interventional
Enrollment
22
Allocation
Randomized
Ages
50 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to determine whether water based or land based group training is more effective for people with COPD.

Read the detailed description

COPD is a more common diagnosis today compared to 20 years ago, and the group is growing fast. The suffering caused by COPD and the financial cost to society is on the increasing. The principal causes of COPD are smoking and inactivity. So far it is poorly understood wich form of exercise is the most effective in training this condition.

02

Conditions studied

  • Chronic Obstructive Pulmonary Disease

Keywords

  • Chronic Obstructive Pulmonary Disease
  • COPD
  • Physical group training
  • Water exercise
  • Cardiorespiratory fitness
  • Functional exercise capacity
  • Health related quality of life
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 22 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
50 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • COPD GOLD II
  • Not taking part in physical activity during the last year

Exclusion criteria

Exclusion Criteria:

  • COPD GOLD I, III, IV
  • Pain in the legs that make activity difficult
05

Study design

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

Study arms

  • Experimental
    B1

    B1 - training in water

    Behavioral: Training in water

  • Experimental
    S1

    S1 - training on land

    Behavioral: Training on land

Interventions

  • BehavioralTraining in water

    45 minutes interval training in water, submaximal intensity, twice a week

  • BehavioralTraining on land

    45 minutes interval training on land, submaximal intensity, twice a week

06

What researchers measure

Primary outcomes

  1. VO2 peak

    Time frame: 12 weeks

Secondary outcomes

  1. Health related quality of life

    Time frame: 12 weeks

07

Study locations

1 site
  • Levanger Hosp
    Levanger, Nord-Trøndelag 7600, Norway
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 7, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00744484
Lead sponsor
Norwegian University of Science and Technology
Collaborators
Helse Nord-Trøndelag HF, Nord-Trøndelag University College
Responsible party
Sponsor
First posted
Sep 1, 2008
Start date
Feb 2008
Primary completion
May 2009
Completion
Sep 2010
Last update
Mar 7, 2022

Study contacts

Thor Naustdal, MD
principal investigator · Hospital of Levanger / NTNU ISB

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

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