<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rutland SB</submitter><funding>NIDDK NIH HHS</funding><pagination>e19413</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7872830</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Cystic fibrosis (CF) is an inherited chronic condition that requires extensive daily care and quarterly clinic visits with a multidisciplinary care team. The limited exchange of information outside of the quarterly clinic visits impedes optimal disease self-management, patient engagement, and shared decision making.&lt;h4>Objective&lt;/h4>The aim of this study is to adapt a mobile health (mHealth) app originally developed in Sweden to the needs of patients, families, and health care providers in a CF center in the United States and to test it as a platform for sharing patient-generated health data with the CF health care team.&lt;h4>Methods&lt;/h4>Focus groups with health care providers of patients with CF, adolescents with CF, and caregivers of children with CF were conducted to de</pubmed_abstract><journal>JMIR formative research</journal><pubmed_title>A Mobile Health Platform for Self-Management of Pediatric Cystic Fibrosis: Qualitative Study of Adaptation to Stakeholder Needs and Integration in Clinical Settings.</pubmed_title><pmcid>PMC7872830</pmcid><funding_grant_id>P30 DK072482</funding_grant_id><pubmed_authors>Geurs R</pubmed_authors><pubmed_authors>Oates GR</pubmed_authors><pubmed_authors>Mims C</pubmed_authors><pubmed_authors>Bergquist RP</pubmed_authors><pubmed_authors>Gutierrez HH</pubmed_authors><pubmed_authors>Rutland SB</pubmed_authors><pubmed_authors>Hager A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Mobile Health Platform for Self-Management of Pediatric Cystic Fibrosis: Qualitative Study of Adaptation to Stakeholder Needs and Integration in Clinical Settings.</name><description>&lt;h4>Background&lt;/h4>Cystic fibrosis (CF) is an inherited chronic condition that requires extensive daily care and quarterly clinic visits with a multidisciplinary care team. The limited exchange of information outside of the quarterly clinic visits impedes optimal disease self-management, patient engagement, and shared decision making.&lt;h4>Objective&lt;/h4>The aim of this study is to adapt a mobile health (mHealth) app originally developed in Sweden to the needs of patients, families, and health care providers in a CF center in the United States and to test it as a platform for sharing patient-generated health data with the CF health care team.&lt;h4>Methods&lt;/h4>Focus groups with health care providers of patients with CF, adolescents with CF, and caregivers of children with CF were conducted to de</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2026-05-03T01:37:28.315Z</modification><creation>2021-02-25T09:07:27Z</creation></dates><accession>S-EPMC7872830</accession><cross_references><pubmed>33496667</pubmed><doi>10.2196/19413</doi></cross_references></HashMap>