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临床试验/NCT02140086
NCT02140086已完成不适用

Buteyko Based Remedial Breathing Therapy With Children With Asthma

ARCIM Institute Academic Research in Complementary and Integrative Medicine2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2014年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
32
试验地点
2
主要终点
Reduction of Betamimetics (-30%) at 3- and/or 6-month follow up

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
6 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • signed informed consent of the parents
  • age 6- 15 years
  • information and consent of the consulting doctor
  • levels of asthma therapy 1-3

排除标准

  • participation in another study

结局指标

主要结局

Reduction of Betamimetics (-30%) at 3- and/or 6-month follow up

时间窗: asthmaspezific parameters are measured before and after intervention as well as 3- and 6- month follow up

次要结局

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

研究者

发起方
ARCIM Institute Academic Research in Complementary and Integrative Medicine
申办方类型
Other
责任方
Sponsor

研究点 (2)

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