Aleshchenko Ekaterina, Langer Thorsten, Calaminus Gabriele, Glogner Juliane, Haugke Henrike, Trocchi Pietro, Swart Enno, Baust Katja
Institute of Social Medicine and Health Systems Research, Faculty of Medicine, Otto von Guericke University, Magdeburg, Germany.
University Hospital of Schleswig-Holstein, Campus Luebeck, Luebeck, Germany.
Cancer Med. 2024 Dec;13(23):e70455. doi: 10.1002/cam4.70455.
The shift from child-centered to adult-focused healthcare presents social and psychological challenges for adolescents and young adults with chronic conditions, which can affect their participation in follow-up care. This study aims to investigate the factors that influence patient-driven motivations for adhering to follow-up recommendations, while also exploring the barriers and supports that impact the transition process for pediatric cancer survivors.
We developed interview guidelines grounded in the Theory of Planned Behavior (TPB) and the stereotype priming model (SPM). We conducted 10 episodic narrative interviews with pediatric cancer survivors during their transition phase. The interview transcripts were analyzed through qualitative thematic content analysis, followed by quantitative analysis using multiple regression models. This research is a part of the broader VersKiK study, which aims to propose enhancements to the organization of (long-term) follow-up care after cancer in childhood and adolescence in Germany.
In this study, pediatric cancer survivors transitioning to adult healthcare showed varied motivations for follow-up care. Positive attitudes, driven by understanding the benefits, improved engagement, while anxiety and fear of losing familiar care created barriers. Family and peer support played a key role in encouraging adherence. Perceived control over healthcare management, supported by organizational help, was crucial, but logistical and financial challenges often undermined this control.
Several motives underlying pediatric cancer survivors' behavior significantly influence their transition experiences. Enhancing positive attitudes, strengthening social support, and improving perceived control through targeted interventions may support smoother transitions to adult healthcare facilities.
Registered at German Clinical Trial Register (IDs: DRKS00025960 and DRKS00026092).
从以儿童为中心的医疗保健向以成人为重点的医疗保健的转变,给患有慢性病的青少年和年轻人带来了社会和心理挑战,这可能会影响他们参与后续护理。本研究旨在调查影响患者遵循后续建议的自主动机的因素,同时探讨影响儿科癌症幸存者过渡过程的障碍和支持因素。
我们以计划行为理论(TPB)和刻板印象启动模型(SPM)为基础制定了访谈指南。我们在儿科癌症幸存者的过渡阶段对他们进行了10次情景叙事访谈。访谈记录通过定性主题内容分析进行分析,然后使用多元回归模型进行定量分析。这项研究是更广泛的VersKiK研究的一部分,该研究旨在提出改进德国儿童和青少年癌症(长期)后续护理组织的建议。
在本研究中,向成人医疗保健过渡的儿科癌症幸存者对后续护理表现出不同的动机。因了解益处而产生的积极态度促进了参与度的提高,而焦虑和对失去熟悉护理的恐惧则造成了障碍。家庭和同伴支持在鼓励坚持方面发挥了关键作用。在组织帮助的支持下,对医疗保健管理的感知控制至关重要,但后勤和财务挑战常常削弱这种控制。
儿科癌症幸存者行为背后的几个动机显著影响他们的过渡经历。通过有针对性的干预增强积极态度、加强社会支持并改善感知控制,可能有助于更顺利地过渡到成人医疗保健机构。
在德国临床试验注册中心注册(标识符:DRKS00025960和DRKS00026092)。