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Clinical Trials/NCT04821908
NCT04821908
Recruiting
Not Applicable

Consequences of SARS-CoV2 Pandemic on Childhood Asthma Control and Exacerbations: French Multicenter Cross-sectional VIRASTHMA COVID G4 Study

University Hospital, Lille1 site in 1 country577 target enrollmentSeptember 14, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma in Children
Sponsor
University Hospital, Lille
Enrollment
577
Locations
1
Primary Endpoint
Controlled asthma
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The SARS-CoV2 pandemic, which emerged in the first quarter of 2020, has led to an unprecedented health crisis in our modern healthcare systems and has resulted in strong national public health measures. The impact of the pandemic and its indirect environmental consequences on pediatric asthma is currently being assessed. In particular, the study of its role on the risk of exacerbations and modification of control is one of the priority research objectives defined by European societies.

The primary aim is to study the impact of the pandemic on asthma control in children aged 3-16 years with a medical diagnosis of asthma, compared to data from other observational cohorts conducted in the same region prior to the pandemic.

A sub-population of children 3-16 years will be assessed at exacerbation and at a follow-up visit, 2-4 months later, with clinical data, biological and microbiological samples.

Detailed Description

Children aged 3-16 years with a medical diagnosis of asthma, will be assessed for asthma control, exacerbation rate. Data will be compared to data from other observational cohorts conducted in the same region prior to the pandemic. A sub-population of children 3-16 years will be assessed at exacerbation and at a follow-up visit, 2-4 months later, with clinical data, biological and microbiological samples.

Registry
clinicaltrials.gov
Start Date
September 14, 2021
End Date
July 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Lille
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Children and adolescents aged 3 to 16 years old
  • With a medical diagnosis of asthma as per-guidelines, who had been followed-up for at least 6 months,
  • Assessed in one of the pediatric departments participating in the study,
  • After written consent of at least one of the 2 parents and/or representative of the parental authority, and of the child if he is older than 8 years old.
  • Criteria for the sub-population assessed at "exacerbation" and second visit:
  • Children and adolescents aged 3 to 16 years
  • With a medical diagnosis of asthma as per-guidelines, who had been followed-up for at least 6 months,
  • Hospitalized for a severe asthma exacerbation (requiring hospitalization and general corticosteroid therapy) at Lille University Hospital
  • After written consent of both parents and/or representative of the parental authority, and of the child if he is over 8 years old

Exclusion Criteria

  • History of chronic respiratory disease other than asthma,
  • Inability of parents to receive informed information, inability to participate in the entire study, refusal to sign the consent form

Outcomes

Primary Outcomes

Controlled asthma

Time Frame: at inclusion

Composite criteria defined by a cACT (4-11 years) or ACT (12-16 years) score ≥ 20 and according to GINA criteria.

Secondary Outcomes

  • Characteristics of asthma(At inclusion and follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • number of infectious episodes in the past year(At inclusion and Follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • Observance(At Inclusion and Follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • history of SARS-Cov2 infection in the past year(At inclusion and Follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • Respiratory virus infection (SARS-CoV2 and other)(at exacerbation and at follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • QoL (Quality of life) in children aged 7-17 years(At Inclusion and Follow-up visit at 2-4 months for the sub-population included at exacerbation)
  • Outdoor levels of pollutants and pollens(At Inclusion and Follow-up visit at 2-4 months for the sub-population included at exacerbation)

Study Sites (1)

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