ISRCTN14489433进行中(未招募)Unknown
Developing and evaluating a mobile phone-based early alert system using high-resolution air quality forecast to improve asthma control in Malaysia
Accord (United Kingdom)0 个研究点目标入组 60 人开始时间: 2023年8月1日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Adult patients aged 18 years old and above with physician-diagnosed asthma and receiving asthma treatment in the previous year
- •2. Adult patients who live in Klang District for the duration of the study
- •3. Patients who had reported poor asthma control and exacerbation aggravated by haze (findings from baseline study in RESPIRE 1)
- •4. Patients who are on controller medication (e.g., an inhaled corticosteroid (ICS), inhaled combination ICS/long-acting beta-agonists (LABA), leukotriene receptor antagonist (LTRA))
- •5. Patients who own and are able to use a smartphone
- •6. Patients who are able to understand the Malay/English language
- •7. Patients who are willing and able to give consent to participate in the study
排除标准
- •1. Patients below 18 years of age
- •2. Patients who have respiratory symptoms (e.g., cough, breathlessness, wheezing) due to other conditions for example established physician diagnoses of:
- •2.1. Respiratory infection e.g., pneumonia, tuberculosis (but not having underlying asthma)
- •2.2. Chronic obstructive pulmonary diseases
- •2.3. Congenital heart disease
- •2.4. Heart, liver or renal failure
- •2.5. Gastro-esophageal reflux
- •2.6. Active life-threatening malignancy and those receiving palliative care
- •3. Patients who have disabilities (physical/psychological) that may interfere with the completion of the study
- •4. Patients who are unwilling or unable to provide written informed consent (e.g. cognitive impairment)
研究者
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