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NCT03598569 Clinical Trial

Auto-evaluation of Dyspnea

Lung Diseases Clinical Trial

Official title:
Dyspnea Evaluated by a Qualified Examiner in Patients With Lung Diseases

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03598569
Other study ID # Autodyspnea
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2013
Est. completion date December 2013

Study information
Verified date June 2018
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary aim of this study was to compare patients-rated evaluation and caregiver's assessment of dyspnea with the standard tools in pulmonology unit (Borg scale and visual analog scale) and the secondary aim was to performed an analysis depending on the diseases (lung cancer vs. other lung diseases) and to verify the agreement between the evaluation between both visual analog scale and modified Borg scale.

Recruitment information / eligibility
Status Completed
Enrollment 271
Est. completion date December 2013
Est. primary completion date July 2013
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- age =18 and

- to have a diagnosis of acute or chronic respiratory disease

Exclusion Criteria:

- mental or cognitive disorders

- inability to understand the local language

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• dyspnea
dyspnea assessment

Locations
Country Name City State
Belgium Cliniques universitaires Saint-Luc Brussels

Sponsors (1)
Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary visual analog scale 3 seconds
Primary borg scale 3 seconds
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