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OpenTrials
Completed

NCT Number: NCT03598569

Auto-evaluation of Dyspnea

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.

Completed

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Key information

Study type

Observational

Primary location

Cliniques universitaires Saint-Luc

Brussels, 1200, Belgium

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

dyspnea

Other

dyspnea assessment

Other names: evaluation

Primary outcomes

  1. visual analog scale

    Time frame: 3 seconds

  2. borg scale

    Time frame: 3 seconds

Sponsors and collaborators

Lead sponsor

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Other

Registry information

Official study title

Dyspnea Evaluated by a Qualified Examiner in Patients With Lung Diseases

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jul 26, 2018
Registry last updated
Jul 26, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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