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ID
Source
Brief title
Health condition
Asthma
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary outcome will be whether the perception is improved after six weeks of home-monitoring and receiving feedback
Secondary outcome
The secondary outcome will be input parameters for a follow-up study
Background summary
Asthmatic children with a bad perception will be included in this study. Those children will receive a home-spirometer and will be asked to measure their asthmatic complaints both subjectively (through a questionnaire including a VAS) and objectively (through performing a spirometry at home). Both outcomes will be combined and feedback will be given to these patients once a week, in total for six weeks. The impact of the given feedback on their perception will be evaluated by comparing the perception at inclusion and the perception after six weeks.
Study objective
There is expected the perception of a patient will be improved after six weeks of home-monitoring and receiving feedback
Study design
A few times a week the participant will perform measurements at home with the NuvoAir Next spirometer and a questionnaire and weekly a feedback session will take place to evaluate these measurements. After six weeks, all the measurements of those weeks will be evaluated to conclude whether the perception is improved. Also, all these measurements will be used for evaluating the secondary outcome: the input parameters for a follow-up study.
Inclusion criteria
Being able to perform spirometry correctly, suffering from moderate to severe asthma and having a bad perception.
Exclusion criteria
Suffering from dysfunctional breathing or exercise induced laryngeal obstructuion (EILO)
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL9638 |
| Other | MEC-U MST : K21-28 |