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Clinical Trials/NCT01345396
NCT01345396
Suspended
Not Applicable

Assessment of an Educational Programme for Pregnant Asthmatic Women on the Level of Asthma Control and Unscheduled Doctor Visits During the Pregnancy

Centre Hospitalier Universitaire Saint Pierre1 site in 1 country80 target enrollmentFebruary 2010
ConditionsAsthma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma
Sponsor
Centre Hospitalier Universitaire Saint Pierre
Enrollment
80
Locations
1
Primary Endpoint
The level of asthma control
Status
Suspended
Last Updated
7 years ago

Overview

Brief Summary

Asthma is the most frequent respiratory disease during pregnancy. In a third of cases, the level of asthma control can decrease during the pregnancy, especially between the 29th and the 36th week. The occurrence of such complications are linked with a high asthma severity level just before the conception and an history of respiratory complications in a previous pregnancy. Many reviews and recommendations claim that pregnant women with asthma should be included in an educational progamme. However, this is poorly studied. The purpose of this study is to observe if an educational programme given before the 20th weeks of gestation has an effect on asthma control until the end of gestation.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
December 2015
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Responsible Party
Principal Investigator
Principal Investigator

Vincent Ninane

Prof. Dr. V. Ninane

Centre Hospitalier Universitaire Saint Pierre

Eligibility Criteria

Inclusion Criteria

  • Pregnant woman (less than 20 weeks of gestation at the inclusion time)
  • Diagnosis of asthma before the pregnancy (clinical history and specific medications used)
  • Agreement to enter into the study

Exclusion Criteria

  • Pregnant woman (more than 20 weeks of gestation at the inclusion time)
  • History of major respiratory problems during previous pregnancy(ies)
  • Refusal to enter into the study

Outcomes

Primary Outcomes

The level of asthma control

Time Frame: Inclusion (baseline), 36 weeks of gestation, 12 weeks post partum

Assessment by the Asthma Control Questionnaire

Secondary Outcomes

  • Number of unscheduled visits to the doctor for asthma(Inclusion (baseline), 36 weeks of gestation, 12 weeks post partum)
  • Quality of life(Inclusion (baseline), 36 weeks of gestation, 12 weeks post partum)
  • Knowledge about asthma(Inclusion (baseline), 36 weeks of gestation, 12 weeks post partum)

Study Sites (1)

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