<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Aleshchenko E</submitter><funding>Federal Joint Committee (G-BA) Innovation Fund in Germany</funding><pagination>e072860</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10860087</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(2)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>This article presents the study design of the qualitative part of the VersKiK study (Long-term care, care needs and wellbeing of individuals after cancer in childhood or adolescence: study protocol of a large scale multi-methods non-interventional study) aiming to explore actual follow-up needs of childhood and adolescence cancer survivors and their informal caregivers, gaps in current follow-up care provision and trajectories of cancer survivors' transition from paediatric to adult healthcare.&lt;h4>Methods and analysis&lt;/h4>We will conduct up to 30 interviews with survivors of childhood and adolescence cancer and their informal caregivers with up to 20 participant observations of follow-up appointments. The results of these will be discussed in up to four focus groups wi</pubmed_abstract><journal>BMJ open</journal><pubmed_title>VersKiK qualitative study design: actual follow-up needs of paediatric cancer survivors, their informal caregivers and follow-up stakeholder perceptions in Germany.</pubmed_title><pmcid>PMC10860087</pmcid><funding_grant_id>01VSF19013</funding_grant_id><pubmed_authors>Voigt M</pubmed_authors><pubmed_authors>Aleshchenko E</pubmed_authors><pubmed_authors>Swart E</pubmed_authors><pubmed_authors>Glogner J</pubmed_authors><pubmed_authors>Langer T</pubmed_authors><pubmed_authors>Baust K</pubmed_authors><pubmed_authors>Calaminus G</pubmed_authors></additional><is_claimable>false</is_claimable><name>VersKiK qualitative study design: actual follow-up needs of paediatric cancer survivors, their informal caregivers and follow-up stakeholder perceptions in Germany.</name><description>&lt;h4>Introduction&lt;/h4>This article presents the study design of the qualitative part of the VersKiK study (Long-term care, care needs and wellbeing of individuals after cancer in childhood or adolescence: study protocol of a large scale multi-methods non-interventional study) aiming to explore actual follow-up needs of childhood and adolescence cancer survivors and their informal caregivers, gaps in current follow-up care provision and trajectories of cancer survivors' transition from paediatric to adult healthcare.&lt;h4>Methods and analysis&lt;/h4>We will conduct up to 30 interviews with survivors of childhood and adolescence cancer and their informal caregivers with up to 20 participant observations of follow-up appointments. The results of these will be discussed in up to four focus groups wi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-04T12:05:57.636Z</modification><creation>2025-04-04T12:05:57.636Z</creation></dates><accession>S-EPMC10860087</accession><cross_references><pubmed>38326270</pubmed><doi>10.1136/bmjopen-2023-072860</doi></cross_references></HashMap>