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Is it possible to have a chronic obstructive pulmonary disease (COPD) specific breathlessness service in the Netherlands?

Not Applicable
Completed
Conditions
Improvement of quality of life in COPD patients with refractory dyspnea
Respiratory
Registration Number
ISRCTN48274234
Lead Sponsor
Spaarne Gasthuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
19
Inclusion Criteria

Patients with COPD (diagnosed by a pulmonologist, post-bronchodilatator FEV1/FVC below the lower limit of normal) were eligible for the study if they experienced refractory dyspnea (troubled by breathlessness despite optimization of COPD treatment) and were able to visit the outpatient clinic.

Exclusion Criteria

1. Terminal phase
2. Cognitive impairment
3. Unable to speak Dutch

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Feasibility outcome: number of patients completing the intervention measured using patient records at the end of the study
Secondary Outcome Measures
NameTimeMethod
<br> 1. Respiratory problems measured using a Dutch translation of the Chronic Respiratory Questionnaire (CRQ), subset mastery domain at baseline and final visit<br> 2. Pulmonary function tests were taken from the patient’s medical file at baseline<br> 3. Patient and professional satisfaction measured using a postal survey with multiple choice questions after the final visit<br>
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