ISRCTN14489433
Active, not recruiting
未知
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 sites60 target enrollmentAugust 1, 2023
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Improving asthma control among adult patients with asthma during increased outdoor pollution.
- Sponsor
- Accord (United Kingdom)
- Enrollment
- 60
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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)
Outcomes
Primary Outcomes
Not specified
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