Assessment of a Mobile App by Adolescents and Young Adults With Cystic Fibrosis: Pilot Evaluation
BackgroundCystic fibrosis (CF) continues to be the most common life-limiting chronic pulmonary disease in adolescents and young adults. Treatment of CF demands a high treatment time investment to slow the progression of lung function decline, the most important contributor to...
Main Authors: | Rudolf, Isa, Pieper, Katharina, Nolte, Helga, Junge, Sibylle, Dopfer, Christian, Sauer-Heilborn, Annette, Ringshausen, Felix C, Tümmler, Burkhard, von Jan, Ute, Albrecht, Urs-Vito, Fuge, Jan, Hansen, Gesine, Dittrich, Anna-Maria |
---|---|
Format: | Article |
Language: | English |
Published: |
JMIR Publications
2019-11-01
|
Series: | JMIR mHealth and uHealth |
Online Access: | https://mhealth.jmir.org/2019/11/e12442 |
Similar Items
-
The human respiratory tract microbial community structures in healthy and cystic fibrosis infants
by: Marie-Madlen Pust, et al.
Published: (2020-12-01) -
Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test
by: Tobias Welte, et al.
Published: (2020-05-01) -
Medical apps in endocrine diseases – hide and seek
by: Urs-Vito Albrecht, et al.
Published: (2014-04-01) -
Description of Cardiological Apps From the German App Store: Semiautomated Retrospective App Store Analysis
by: Albrecht, Urs-Vito, et al.
Published: (2018-11-01) -
VJ Segment Usage of TCR-Beta Repertoire in Monozygotic Cystic Fibrosis Twins
by: Sebastian Fischer, et al.
Published: (2021-02-01)