Children with cancer and their families after active treatment: analyses of biopsychosocial needs and implications for healthcare - a study protocol.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
05 04 2022
Historique:
entrez: 6 4 2022
pubmed: 7 4 2022
medline: 8 4 2022
Statut: epublish

Résumé

Patients and families affected by paediatric cancer experience psychosocial burden not only during active treatment but also during follow-up care. Use of health services during follow-up treatment should be organised according to patients' and family members' needs with regard to their physical and mental situation. This study aims (1) at analysing healthcare use (medical and psychosocial) and associated factors in follow-up care of paediatric cancer patients and (2) at investigating the psychosocial situation and support needs of children and their families during follow-up care. Based on the results, recommendations for healthcare planning and for the development of new and the optimisation of existing support offers will be derived. We will conduct a prospective observational study using a naturalistic explorative design with quantitative and qualitative methods. Paediatric cancer patients in follow-up care, their parents and siblings will be invited to fill out a questionnaire at three measurement points (baseline, 6 months follow-up, 12 months follow-up; target n=252 complete data sets over all measurement points). Additionally, parents will be interviewed using a semistructured interview guideline (target n=15-20) at baseline. Quantitative data will be analysed using descriptive statistics, linear mixed models and regression models. Moreover, explorative analyses will be conducted. Qualitative data will be analysed using qualitative content analyses. The study was approved by the Local Psychological Ethics Committee (LPEK-0281). Our findings will be published in scientific, peer-reviewed journals and presented to clinicians and researchers on conferences. To assure that results will be available to affected patients and families, a lay summary will be written and disseminated using several ways (upload on the homepage of the research group, upload on the homepage of the psychosocial working group in the Society for Paediatric Oncology/Haematology in Germany, sending to relevant patient organisations). DRKS00025289.

Identifiants

pubmed: 35383068
pii: bmjopen-2021-055633
doi: 10.1136/bmjopen-2021-055633
pmc: PMC8984037
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e055633

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

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Auteurs

Laura Inhestern (L)

Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany l.inhestern@uke.de.

Verena Paul (V)

Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Jana Winzig (J)

Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Stefan Rutkowski (S)

Clinic of Pediatric Hematology and Oncology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Gabriele Escherich (G)

Clinic of Pediatric Hematology and Oncology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Corinna Bergelt (C)

Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Medical Psychology, University Medicine Greifswald, Greifswald, Germany.

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Classifications MeSH