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临床试验/ISRCTN14489433
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

发起方
Accord (United Kingdom)

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