Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
32 participants
INTERVENTIONAL
2015-07-31
2016-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Buteyko
Children in the intervention group will perform 6 sessions (twice a week) of treatment with the Buteyko Method.
Buteyko
Intervention will be held twice a week during 3 weeks.
Asthma education
Children assigned to the control group will receive, along with their parents, educational interventions in relation to asthma.
Asthma education
Educational interventions in relation to asthma will be given to children assigned to the control group.
Interventions
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Buteyko
Intervention will be held twice a week during 3 weeks.
Asthma education
Educational interventions in relation to asthma will be given to children assigned to the control group.
Eligibility Criteria
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Inclusion Criteria
* Regular inhaled corticosteroids with no change in dose in the preceding 4 weeks;
* Children cannot present: other respiratory disease (such as cystic fibrosis, bronchiectasis, tuberculosis), retinal detachment, hypertensive crisis, congenital heart defect, pulmonary edema, history of lobectomy or lung segmentectomy, respiratory infections 15 days prior to the evaluations.
Exclusion Criteria
* Give up participating in the research and present acute symptoms of respiratory tract during the assessments.
7 Years
12 Years
ALL
No
Sponsors
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Universidade Federal do Rio Grande do Norte
OTHER
Responsible Party
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Karla Morganna Pereira Pinto de Mendonça
Principal investigator
Locations
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Universidade Federal do Rio Grande do Norte (UFRN)
Natal, Rio Grande do Norte, Brazil
Countries
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Other Identifiers
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562.554
Identifier Type: -
Identifier Source: org_study_id
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