ASPECT: Child Asthma : What Parents Attitude During an Asthma Attack at Home Before Consulting the Pediatric Emergencies

Sponsor
University Hospital, Brest (Other)
Overall Status
Completed
CT.gov ID
NCT03967873
Collaborator
(none)
350
2
20.7
175
8.5

Study Details

Study Description

Brief Summary

prospective multicenter observational study. Parents whose children meet the inclusion criteria complete a questionnaire assessing the child's follow-up, the management of the current asthma attack, and the treatment provided at home.

The main objective is to calculate the prevalence of placement of short-acting bronchodilators. The secondary objectives are to describe the factors associated with their implementation.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    350 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prevalence of Preoperative Short-acting Mimetic beta2 Therapy by Parents of Asthmatic Children Attending Emergency Room for Asthma Attack
    Actual Study Start Date :
    Oct 9, 2018
    Actual Primary Completion Date :
    Jun 30, 2020
    Actual Study Completion Date :
    Jun 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. prevalence of short-acting bronchodilator induction in children attending emergency room for asthma attack [1 hour]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    2 Years to 15 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • child over 2 years emergency room consultant for asthma attack

    • child whose parents did not express their opposition to participate and completed the non-objection form

    • child consultant in pediatric emergencies of Quimper and Brest

    Exclusion Criteria:
    • child whose age is not between 2 and 15 years old

    • cough equivalent of asthma

    • history of cardiac or pulmonary pathology or prematurity

    • refusal to participate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHRU de Brest Brest France 29609
    2 Ch Quimper Quimper France 29000

    Sponsors and Collaborators

    • University Hospital, Brest

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Brest
    ClinicalTrials.gov Identifier:
    NCT03967873
    Other Study ID Numbers:
    • ASPECT (29BRC18.0201)
    First Posted:
    May 30, 2019
    Last Update Posted:
    Aug 24, 2020
    Last Verified:
    Aug 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 24, 2020