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Multiprofessional Advance Care Planning and Shared Decision Making for End of Life Care (MAPS)

2016年6月3日 更新者:University of Zurich

Multiprofessional Advance Care Planning and Shared Decision-making for End of Life Care MAPS Trial

Multiprofessional Advance Care Planning and shared decision making for end of live care for terminal patients and their relatives.

The aim of this study is to develop, implement and test a complex intervention for improving patients' preparation for and participation in end of life decisions. In cooperation with local, national and international partners, the investigators will focus on strategies to enhance advance care planning and shared decision making on end of life issues, and documentation and transferability of end of life decisions across health care settings in coordinated approach involving patients, their families and care givers (in and out of hospital).

研究概览

研究类型

介入性

注册 (实际的)

115

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • ZH
      • Zurich、ZH、瑞士、8091
        • University Hospital Zurich, Clinical Ethics

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion criteria: -patients in which the treating physician on the ward would not be surprised if the patient died during the next year (surprise question of Weissman et al 2011)

  • male and female patients above 18 years of age
  • signed informed consent after being informed
  • patients able to appoint a surrogate decision maker (SM) and/or responsible physician to be contacted after discharge

Exclusion criteria: -patients not capable of speaking german

  • patients having no responsible physician to be contacted after discharge and no relative/future surrogate decision maker (SM)
  • inhouse patients being discharged within the next 2 days or ambulatory patients not regularly coming to the wards (at least every two month)
  • patients assessed by their physician to be in obvious denial of their situation (illness/prognosis)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
有源比较器:Control Group
A routine care discharge planning with the social service
A routine care discharge planning with the social service
实验性的:Advance Care Planning ACP

Patient get a decision aid video and library and up to 3 consultations with qualified Advance Care Planning Facilitators.

--------------------------------------------------------------------------------

Patient of the intervention group get a decision aid video and library and up to 3 consultations with qualified Advance Care Planning Facilitators.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
end of life wish on resuscitation known (if alive) or fulfilled(if dead) after 6 month by responsible physician and/or surrogate decision maker (SM)
大体时间:during 2 weeks six months after discharge
during 2 weeks six months after discharge

次要结果测量

结果测量
大体时间
end of live decisions on last place of care, antibiotics for pneumonia, feeding tube, intravenous fluids, dialysis, intubation and sedation,
大体时间:during 2 weeks six months after discharge
during 2 weeks six months after discharge
decisional conflict scale ("DCS"), O Connor et al 1995
大体时间:at discharge and during 2 Weeks six months after discharge
at discharge and during 2 Weeks six months after discharge
Satisfaction with information and care, (see Detering et al 2010)
大体时间:at discharge
at discharge
Hospital Anxiety and Depression scale ("HADS")
大体时间:discharge and during 2 weeks six months after discharge
discharge and during 2 weeks six months after discharge
Having an Advance directive
大体时间:at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
Having an appointed surrogate decision maker
大体时间:at discharge, during 2 weeks three month after discharge and during 2 weeks six month after discharge
at discharge, during 2 weeks three month after discharge and during 2 weeks six month after discharge
Any hospital stay
大体时间:during 2 weeks three months after discharge and during 2 weeks six months after discharge
during 2 weeks three months after discharge and during 2 weeks six months after discharge
Decisions regarding end of life issues already having been made/taken place
大体时间:during 2 weeks six months after discharge
during 2 weeks six months after discharge
open question on important medical decisions being made
大体时间:during 2 weeks three months after discharge
during 2 weeks three months after discharge
Treatment against patients wishes
大体时间:during 2 weeks three months after discharge and during 2 weeks six months after discharge, or 3 month after death
during 2 weeks three months after discharge and during 2 weeks six months after discharge, or 3 month after death
Distress of Patients or relatives because of content of the consultation
大体时间:at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Tanja Krones, MD、University Hospital Zurich, Clinical Ethics

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2013年7月1日

初级完成 (实际的)

2015年4月1日

研究完成 (实际的)

2015年8月1日

研究注册日期

首次提交

2012年11月26日

首先提交符合 QC 标准的

2013年7月30日

首次发布 (估计)

2013年8月2日

研究记录更新

最后更新发布 (估计)

2016年6月6日

上次提交的符合 QC 标准的更新

2016年6月3日

最后验证

2016年6月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • MAPS Trial

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