Patient, Relative and Staff Experiences of Clinical Trial Participation in Neurooncology: "Maybe You Can Also Show the Positive, No Matter How It Ends".

IF 2.5 4区 医学 Q3 ONCOLOGY Cancer Management and Research Pub Date : 2024-06-21 eCollection Date: 2024-01-01 DOI:10.2147/CMAR.S447407
Ronja Thallner, Christoph Gumbinger, Anja Hohmann, Antje Wick, Wolfgang Wick, Loraine Busetto
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Abstract

Purpose: There is a lack of evidence regarding how patients with malignant brain tumor and their relatives experience participation in neurooncological clinical trials. Similarly, insights from the perspective of trial staff caring for this group of patients are missing. This study aims to investigate patient, relative and trial staff experiences regarding participation in clinical neurooncological trials.

Methods: Within a qualitative exploratory study, 29 semi-structured interviews with brain tumor patients, relatives and trial staff were conducted and analyzed using reflexive thematic analysis (RTA) by Braun and Clarke. A patient researcher and patient council were involved in data analysis and interpretation.

Results: Four themes were developed reflecting significant aspects of the trial experience: 1. "It all revolves around hope"; 2. "Trial participation: experiencing unique medical care"; 3. "Everyone's roles are changing"; 4. "Communication as a possible area of conflict". Experiencing trial participation and general medical treatment were found to be interconnected to such a degree that they were often not meaningfully distinguished by patients and relatives.

Conclusion: In addition to assessing traditional endpoints for patient outcomes, we recommend increased emphasis on investigating the impact of the "soft" components constituting trial participation. Due to the interconnectedness of medical treatment and trial participation, we recommend further investigation in comparison to experiences in regular care. A deeper understanding of trial participation is needed to inform improvements for patient experiences and staff satisfaction alongside medical and scientific progress.

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患者、亲属和工作人员参与神经肿瘤学临床试验的经历:"无论结局如何,也许你也能看到积极的一面"。
目的:关于恶性脑肿瘤患者及其亲属参与神经肿瘤临床试验的经历,目前还缺乏相关证据。同样,也缺乏从护理这类患者的试验工作人员角度出发的见解。本研究旨在调查患者、亲属和试验人员参与神经肿瘤临床试验的经历:在一项定性探索性研究中,对脑肿瘤患者、亲属和试验工作人员进行了 29 次半结构式访谈,并采用布劳恩和克拉克的反思性主题分析法(RTA)进行了分析。一名患者研究员和患者委员会参与了数据分析和解释:结果:形成了四个主题,反映了试验体验的重要方面:1.1. "一切都围绕着希望";2. "参与试验:体验独特的医疗护理";3. "每个人的角色都在改变";4. "沟通是可能存在冲突的领域"。我们发现,参与试验和一般医疗在很大程度上是相互关联的,以至于患者和亲属往往无法对其进行有意义的区分:结论:除了评估患者预后的传统终点外,我们建议更加重视调查构成试验参与的 "软 "因素的影响。由于医疗与试验参与的相互关联性,我们建议将其与常规护理中的经验进行比较,并开展进一步调查。我们需要更深入地了解试验参与,以便在医疗和科学进步的同时,为改善患者体验和提高员工满意度提供信息。
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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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