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Buteyko Based Remedial Breathing Therapy With Children With Asthma

Not Applicable
Completed
Conditions
Asthma
Registration Number
NCT02140086
Lead Sponsor
ARCIM Institute Academic Research in Complementary and Integrative Medicine
Brief Summary

A randomized, controlled trial to investigate the effects of a buteyko based remedial breathing therapy on children with asthma regarding to their symptoms, use of medication and lung function tests.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • signed informed consent of the parents
  • age 6- 15 years
  • information and consent of the consulting doctor
  • levels of asthma therapy 1-3
Exclusion Criteria
  • participation in another study

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Reduction of Betamimetics (-30%) at 3- and/or 6-month follow upasthmaspezific parameters are measured before and after intervention as well as 3- and 6- month follow up
Secondary Outcome Measures
NameTimeMethod
Paediatric asthma caregiver´s quality of life questionnaire (PACQLQ)parameters are measured before and after intervention as well as 3- and 6- month follow up
NO-measurement nasal and oralparameters are measured before and after intervention as well as 3- and 6- month follow up
parameters of spirometryparameters are measured before and after intervention as well as 3- and 6- month follow up
Asthma Control Questionnaire (ACQ)parameters are measured before and after intervention as well as 3- and 6- month follow up

Scores of the ACQ (Asthma Control Questionnaire)

Paediatric Asthma Quality of Life Questionnaire (PAQLQ)parameters are measured before and after intervention as well as 3- and 6- month follow up

Scores of PAQLQ (Paediatric Asthma Quality of Life Questionnaire)

Buteyko-Questionnaireparameters are measured before and after intervention as well as 3- and 6- month follow up
ARCIM Questionnaire (AFB)parameters are measured before and after intervention as well as 3- and 6- month follow up

Scores of the AFB (ARCIM Questionnaire) regarding to asthma symptoms of the last 3 month (AFB is not validated)

Peak Flowparameters are measured before and after intervention as well as 3- and 6- month follow up

Trial Locations

Locations (1)

Filderklinik

🇩🇪

Filderstadt, Baden-Württemberg, Germany

Filderklinik
🇩🇪Filderstadt, Baden-Württemberg, Germany

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