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Clinical Trials/NCT01512043
NCT01512043
Completed
Not Applicable

Breathing Control in Patients With Chronic Obstructive Pulmonary Disease (COPD) Intervention With Device-guided Breathing Control in COPD

Lovisenberg Diakonale Hospital1 site in 1 country150 target enrollmentJuly 2011
ConditionsCOPD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD
Sponsor
Lovisenberg Diakonale Hospital
Enrollment
150
Locations
1
Primary Endpoint
Breathlessness
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
September 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Lovisenberg Diakonale Hospital
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Breathlessness

Time Frame: 4 months

Questionnaires

Secondary Outcomes

  • Depression(4 months)
  • Quality of life(4 months)
  • Pulmonary functional tests(4 months)
  • Fatigue(4 months)
  • Sleeping difficulties(4 months)
  • Pain(4 months)
  • Anxiety(4 months)
  • 6. Min walk test(4 months)
  • Arterial blood gas measures(4 months)

Study Sites (1)

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