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Breathing Control in Patients With Chronic Obstructive Pulmonary Disease (COPD)

L

Lovisenberg Diakonale Hospital

Status

Completed

Conditions

COPD

Treatments

Behavioral: Breathing control

Study type

Interventional

Funder types

Other

Identifiers

NCT01512043
2009/2/0285

Details and patient eligibility

About

There is a demand for explorative and comparative studies on various non-pharmaceutical efforts in treating and helping chronic obstructive pulmonary disease patients. This study has been developed in light of this need. The main purpose of the project is to test whether a device guided breathing control system can decreasing the feeling of breathlessness in patients with moderate stage and severe stage of COPD. In addition the study could shed light on whether a reduced feeling of breathlessness can lead to improved physical function, and less experience of other symptoms (I.e., depression, anxiety, sleeping difficulties, fatigue, pain) and provide a better quality of life for patients with COPD.

Enrollment

150 patients

Sex

All

Ages

30+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Dyspnoea symptoms in daily life
  • Spirometry values showing a COPD moderate stage II (FEV1/FVC<70%, FEV1<80%) and severity grade at a severe stage III (FEV1/FVC<70%, FEV1<50% and FEV1 = 30% of a predicted)
  • Be able to read, write and speak Norwegian
  • Be at a stable phase of the disease

Exclusion criteria

  • Changes in pulmonary medication during the last 4 weeks
  • Diagnosis of cancer
  • Presently attending a pulmonary rehabilitation course or other similar COPD education courses (due to the fact that these courses often have instructions on breathing control), or having attended similar courses during the last six months
  • Ongoing exacerbation
  • Attending other competitive studies
  • Diagnosis of neuromuscular disease
  • Diagnosis of dementia
  • Attending help from a pulmonary physiotherapist

Trial design

150 participants in 3 patient groups

1. Breathing control
Experimental group
Description:
Description ...
Treatment:
Behavioral: Breathing control
2. Listening to music
Active Comparator group
Description:
Listening to music without guiding on breathing on the same device as breathing control twice a day for four weeks. Using the device to measure breathing movements.
Treatment:
Behavioral: Breathing control
3. Silence
Sham Comparator group
Description:
Using the device to measure breathing movement twice a day for four weeks. No instruction on breathing control and no music.
Treatment:
Behavioral: Breathing control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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