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Clinical Trials/NCT03798158
NCT03798158RecruitingNot Applicable

Prevalence and Characterization of Persistent Dyspnea After an Hospitalization for a Respiratory Disease

Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil1 site in 1 country150 target enrollmentStarted: April 11, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
150
Locations
1
Primary Endpoint
Prevalence of persistent dyspnea in the end of an hospitalization for a a respiratory disease

Study Overview

Brief Summary

The investigators aim to make an overview of persistent dyspnea at the end of an hospitalization for a respiratory disease using an actual tool, the Multidisciplinary Dyspnea Profile questionnaire.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age over 18 years old
  • Able to respond the questionnaire
  • Presenting at admission a dyspnea over 3/10 on numerical analogic scale
  • Admitted for a respiratory cause

Exclusion Criteria

  • cognitive impairment
  • no french-speaking person

Outcomes

Primary Outcomes

Prevalence of persistent dyspnea in the end of an hospitalization for a a respiratory disease

Time Frame: An average of one week, until the end of the hospitalization

Secondary Outcomes

  • Outcome of patients with persistent dyspnea after hospitalization(6 months)
  • Characterization of persistent dyspnea using MDP(An average of one week, until the end of the hospitalization)

Investigators

Sponsor
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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