Wearable cough registration to assess children’s asthma control
- Conditions
- Asthma, Bronchial hyperresponsiveness, Children, Astma, Bronchiale Hyperreactiviteit, Kinderen.
- Registration Number
- NL-OMON20576
- Lead Sponsor
- MST Enschede
- Brief Summary
o publications yet.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
•Children with paediatrician diagnosed asthma, or children whom are suspected to suffer from asthma, based on reported symptoms, atopy and physical examination performed by a physician.
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
•Children who are unable to speak Dutch, or whose legal guardians are unable to speak Dutch.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study parameter is to correlate the cough sound parameters to ECT-determined asthma control, reflected by the behaviour of the FEV1 during the ECT.
- Secondary Outcome Measures
Name Time Method