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临床试验/NCT01362816
NCT01362816已完成不适用

The European Palliative Care Cancer Symptom Study (EPCCS). A Prospective Data Collection

Norwegian University of Science and Technology1 个研究点 分布在 1 个国家目标入组 1,739 人开始时间: 2011年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,739
试验地点
1
主要终点
change in cancer symptoms

研究概览

简要总结

The rising incidence of cancer and the rapidly increasing number of people living longer with incurable disease, accentuates the need for optimal symptom management throughout the disease trajectory. Thanks to the medical and technological development, and the increased interest in palliative care research, palliative medicine has gradually become more evidence based. Patients with advanced cancer experience multiple symptoms at the time with fluctuating intensity and severity. Pain, fatigue, nausea/vomiting, dyspnea, loss of appetite and depression are among the most common and experienced by more than 50%. However, the prevalence rates of these symptoms vary considerably across studies, with a range from 35 to 90 % for pain as an example. These differences may in part be explained by different assessment tools, study methods and design and population characteristics. There is also lack of agreed-upon, common criteria to describe the main characteristics of a palliative care cancer population and few standardized tools for assessment and classification of symptoms exist. These shortcomings limit the possibility to design randomized controlled treatment trials in palliative care; the optimal way to improve clinical symptom management. To do this, a better understanding of how symptoms evolve and how they should be assessed and classified throughout the palliative care disease trajectory is important, supplemented with registrations of the treatment provided. The primary aim of this international research project the European Palliative Care Cancer Symptom study (EPCCS) is to extend the knowledge about and gain new insight in the prevalence and development of the most frequent cancer related symptoms during the course of disease, in a large sample of palliative care cancer patients. The clinical usefulness of the new assessment and classification system developed by the European Palliative Care Research Collaborative (EPCRC) / European Association for Palliative Care Research Network (EAPC RN) will be examined and data on the organization and delivery of palliative care at participating centers will be collected. The project also aims to further develop and consolidate international research collaboration through the European Palliative Care Research Centre (PRC). Taken together, these efforts will increase the understanding of the palliative disease trajectory and provide necessary knowledge and structure for future randomized controlled trials (RCTs)

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient has a cancer diagnosis (radiological, histological, cytological or operative evidence)
  • Local, loco-regional or metastatic disease
  • Defined as a palliative care patient; enrolled in a palliative care programme
  • Age 18 years or older
  • Able to provide written informed consent
  • Able to complete the data collection tool, preferably without help
  • Available for follow up registration

排除标准

  • Patients receiving anti-cancer treatment with a curative intent
  • Patients who are unable to complete the registration due to language problems or severe physical problems
  • Patients who have psychotic disorders or obvious cognitive impairment
  • Patients who cannot come for regular follow-up visits, due to geographical or social reasons

结局指标

主要结局

change in cancer symptoms

时间窗: up to 6 months

assessment and classification system developed by the European Palliative Care Research Collaborative (EPCRC) / European Association for Palliative Care Research Network (EAPC RN)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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