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ABSTRACT: Background
Medical treatment for children with Juvenile Idiopathic Arthritis (JIA) has improved radically since the development of biological disease-modifying antirheumatic drugs. However, children suffer from pain and anxiety, and parents often experience loneliness and lack of support. Some parents reported that information provided at the time their child was diagnosed could be difficult to assimilate. Therefore, the aim of this study was to develop a Juvenile Arthritis Support Program (JASP-1) for children recently diagnosed with JIA and their parents. Moreover, the aim was to explore patients´ and parents´ experiences with JASP-1 and its potential impact on patients´ physical health.Methods
JASP-1 included seven patient- and family-centered clinical visit from time of
SUBMITTER: Mordrup K
PROVIDER: S-EPMC11325655 | biostudies-literature | 2024 Aug
REPOSITORIES: biostudies-literature