Publications by authors named "Maximilian Hopfgartner"

Article Synopsis
  • * It uses an adapted CFIR questionnaire to analyze responses from 31 healthcare professionals, highlighting that while the interventions themselves are seen positively, resource shortages, poor policy integration, and lack of incentives are major obstacles.
  • * Recommendations to overcome these barriers include designing patient-focused tools, creating user manuals, conducting workshops, and enhancing communication through interdisciplinary meetings, alongside integrating psychosocial care into public health policies to improve treatment standards.
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Pediatric cancer is one of the most burdensome chronic diseases, necessitating a variety of severe medical interventions. As a result, the disease and its treatment cause numerous acute and long-term medical, psychological, and socioeconomic strains for young patients and their families. Therefore, psychosocial care using evidence-based interventions (EBIs) before, during, and after medical treatments is essential to ensure that patients receive adequate information and to minimize the adverse emotional and psychosocial impacts such as insecurity, fear, and shame.

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Background: Patient and public involvement and engagement (PPIE) in healthcare research is crucial for effectively addressing patients' needs and setting appropriate research priorities. However, there is a lack of awareness and adequate methods for practicing PPIE, especially for vulnerable groups like childhood cancer survivors.

Aims: This project aimed to develop and evaluate engagement methods to actively involve pediatric oncological patients, survivors, and their caregivers in developing relevant research questions and practical study designs.

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Objective: The present report describes the results of four delphi surveys conducted within the quality improvement project "My Logbook" which aims to translate evidence-based standards for psychosocial care in pediatric oncology into a practical consensus-based tool.

Methods: In four consecutive delphi surveys a total of n=153 international, multi-disciplinary experts rated the content, method, and design of the different booklets of "My Logbook" which a local expert group had conceptualized. After each survey, the feedback was incorporated, and the changes were evaluated in a final consensus vote by the quality assurance panel of the PSAPOH.

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Background: Psychosocial guidelines and standards systematically describe stressors and resources in particularly challenging situations and hence serve as a basis for interventions to achieve defined psychosocial goals. Despite fundamental principles and guidelines for psychosocial methods, the quality of provided care varies considerably depending on setting, provision, and profession. The purpose of the present protocol is to illustrate the development and evaluation of the standardized psychological intervention "My Logbook", a practical guide accompanying children through all stages of treatment by directly translating current quality standards of psychosocial care into practice.

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Article Synopsis
  • Public and Patient Involvement and Engagement (PPIE) in research is underutilized, despite evidence indicating that it enhances care quality and patient satisfaction in pediatric oncology.
  • The project evaluated knowledge and attitudes toward PPIE among healthcare professionals and patients across Europe through surveys and workshops, revealing a general lack of understanding of PPIE terminology and concepts.
  • Findings from the project will be used to develop a tailored training tool aimed at improving stakeholder involvement in PPIE within pediatric oncology research.
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