Feasibility Study for a Multi-centre Trial Investigating Whether Physiotherapy Improves Outcomes for Children With Dysfunctional Breathing
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 31
- 试验地点
- 2
- 主要终点
- Child and parent proxy report versions of the quality of life questionnaire(PedsQL)
研究概览
简要总结
Dysfunctional breathing in children primarily affects the ability to participate in sport or exercise but can also stop children doing other activities such as playing musical instruments. Clinical experience has shown that physiotherapy (through the use of breathing retraining and other associated techniques) can stop the symptoms of dysfunctional breathing, allowing children to return to normal activities and reduce or stop inhaled medications.
Whilst there is some evidence in adults with this condition to support the use of physiotherapy, there have been no studies carried out in children investigating whether physiotherapy is beneficial for children with dysfunctional breathing.
This study therefore aims to investigate the feasibility of a future large scale multicentre clinical trial designed to investigate whether physiotherapy improves outcomes for children with dysfunctional breathing. The improved management of this common but under recognised condition would lead to significant improvements in the quality of life of children coupled with the reduction in potentially harmful medications.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 8 Years 至 16 Years(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Aged 8-16 years Clinical diagnosis of dysfunctional breathing
排除标准
- •Uncontrolled comorbidities Participant and parents/guardians not fluent in written and spoken English Inability to follow instructions
结局指标
主要结局
Child and parent proxy report versions of the quality of life questionnaire(PedsQL)
时间窗: 24 months
To measure participant and parent proxy report of quality of life in the four domains of physical, emotional, social and school functioning
次要结局
- Symptom questionnaire (Nijmegen questionnaire)(24 months)
- Structured light plethysmography (SLP) scan (Thora-3DI)(24 months)
- Reliever inhaler usage recorded using a data logger device(24 months)
