Vanbutsele Gaëlle, Van Belle Simon, De Laat Martine, Surmont Veerle, Geboes Karen, Eecloo Kim, Pardon Koen, Deliens Luc
End-of-Life Care Research Group, Vrije Universiteit Brussel & Ghent University, Laarbeeklaan 103, 1090, Brussels, Belgium.
Palliative care team, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium.
BMC Health Serv Res. 2015 Dec 15;15:554. doi: 10.1186/s12913-015-1207-3.
Previous studies in the US and Canada, have shown the positive impact of early palliative care programs for advanced cancer patients on quality of life (QoL) and even survival time. There has been a lack of similar research in Europe. In order to generalize the findings from the US and Canada research on a larger scale, similar studies are needed in different countries with different care settings. The aim of this paper is to describe the research protocol of a randomized controlled trial, situated in Flanders, Belgium, evaluating the effect of systematic early integration of palliative care in standard oncology care.
METHODS/DESIGN: A randomized controlled trial will be conducted as follows: 182 patients with advanced cancer will be recruited from the departments of Medical Oncology, Digestive Oncology and Thoracic Oncology of the Ghent University Hospital. The trial will randomize patients to either systematic early integration of palliative care in standard oncology care or standard oncology care alone. Patients and informal caregivers will be asked to fill out questionnaires on QoL, mood, illness understanding and satisfaction with care at baseline, 12 weeks and every six weeks thereafter. Other outcome measures are end-of-life care decisions and overall survival time.
This trial will be the first randomized controlled trial in the Belgian health care setting to evaluate the effect of systematic early integration of palliative care for advanced cancer patients. The results will enable us to evaluate whether systematic early integration of palliative care has positive effects on QoL, mood and patient illness-understanding and which components of the intervention contribute to these effects.
Clinicaltrials.gov Identifier: NCT01865396 , registered 24(th) of May, 2013.
美国和加拿大此前的研究表明,针对晚期癌症患者的早期姑息治疗方案对生活质量(QoL)乃至生存时间都有积极影响。欧洲缺乏类似研究。为了在更大范围内推广美国和加拿大研究的结果,需要在不同国家、不同护理环境下开展类似研究。本文旨在描述一项位于比利时弗拉芒地区的随机对照试验的研究方案,该试验旨在评估将姑息治疗系统地早期整合到标准肿瘤护理中的效果。
方法/设计:将进行如下随机对照试验:从根特大学医院的医学肿瘤学、消化肿瘤学和胸肿瘤学部门招募182名晚期癌症患者。试验将把患者随机分为两组,一组接受将姑息治疗系统地早期整合到标准肿瘤护理中的方案,另一组仅接受标准肿瘤护理。患者和非正式照护者将被要求在基线、12周以及此后每六周填写关于生活质量、情绪、对疾病的理解以及对护理满意度的问卷。其他结局指标为临终护理决策和总生存时间。
该试验将是比利时医疗保健环境中首个评估将姑息治疗系统地早期整合到晚期癌症患者护理中的效果的随机对照试验。研究结果将使我们能够评估姑息治疗的系统早期整合是否对生活质量、情绪和患者对疾病的理解有积极影响,以及干预措施的哪些组成部分促成了这些影响。
Clinicaltrials.gov标识符:NCT01865396,于2013年5月24日注册。