Wearable technology to assess children’s asthma control in the home-situatio
Recruiting
- Conditions
- Pediatric asthma / astma bij kinderenBronchial hyperresponsiveness (BHR) / bronchiale hyper reactiviteitExercise induced bronchoconstriction (EIB) / inspanningsastma
- Registration Number
- NL-OMON23181
- Lead Sponsor
- Medisch Spectrum Twente (MST, Enschede)
- Brief Summary
o publications yet.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Phase 1 (60 patients):
•Children with paediatric based asthma.
Exclusion Criteria
Both phase 1 and phase 2:
•Children with an inability to understand or speak Dutch. This also applies for the parents of all children below the age of 12.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of this study is the asthma control. This categorical variable will be tested for its agreement with the measured home-measured parameters.
- Secondary Outcome Measures
Name Time Method *Accuracy and reproducibility of the wearable devices.<br /><br>*Asthma severity in non controlled asthma patients and its relation to the wearable data.<br /><br>*Patient perception of asthma control. <br /><br>*The agreement of the Exhaled biomarker measurement with asthma control.<br>