ACTRN12621001280897尚未招募未知
A clinical trial examining the effects of SingINg For breathing on quality of life in COPD aNd ILD pAtients
St Vincents Hospital Melbourne0 个研究点目标入组 140 人开始时间: 2021年9月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 140
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patient Cohort:
- •1.Participants with a confirmed diagnosis of COPD or ILD
- •Diagnosis confirmed on either CT chest scan (within the last 5 years) or lung function testing (within the last 2 years)
- •2.On stable treatment for at least 4 weeks
- •Has not started any new or changed existing cardiorespiratory medications (including antibiotics and oral steroids). To be determined by study site clinician.
- •Has not been admitted to hospital with an exacerbations of their underlying disease (COPD or ILD) within the past 4 weeks.
- •3.Modified Medical Research Council dyspnoea score grerater than or equal to 2
- •4.Aged 18 years or over
- •5.Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
- •Carers Cohort (optional):
- •1.Nominated carers of eligible patients will be eligible to participate.
- •2.Aged 18 years or over
- •3.Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
排除标准
- •1.Participants cannot be actively undertaking a centre-based pulmonary rehabilitation program. However past completion of such a program is permitted.
研究者
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