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Introduction of a Dyspnea Service in the Netherlands

Introduction of a Dyspnea Service in the Netherlands - Introduction of a Dyspnea Service in the Netherlands

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48131
Enrollment
20
Registered
2019-08-09
Start date
2019-07-01
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD

Interventions

See under Study design.

Sponsors

Spaarne Gasthuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - COPD, diagnosed by a pulmonologist, with postbronchodilatator FEV1/FVC below the lower limit of normal - refractory dyspnea (troubled by breathlessness in spite of optimization of COPD treatment, MRC dyspnea score at least 2 points). - able to visit the outpatient clinic - able to read and understand the Dutch language - mentally competent, as assessed by recruiting health care professional

Exclusion criteria

Exclusion criteria: - An acute exacerbation of COPD, leading to hospitalisation, in 6 weeks before inclusion. - An acute exacerbation during the study period, will lead to exclusion with the possibility to re-enter after stabilization. In that case, patients will follow the same study procedures again. - Active participation in another trial

Design outcomes

Primary

MeasureTime frame
Main feasibility criteria: 1. 75% of included patients complete the intervention.

Secondary

MeasureTime frame
1. Description of components and practical aspects of ADD. 2. semi-structured interviews with patients and carers to evaluate ADD after six weeks.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)