跳至主要内容
临床试验/NL-OMON54372
NL-OMON54372已完成不适用

The iLIVE project: Live well, die well. A research programme to support living until the end - iLIVE cohort study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • 1. Patient is 18 years or older.
  • 2. The patient is aware that recovering from his/her disease is unlikely, to be
  • assessed by the attending physician.
  • 3. The attending physician would not be surprised if the patient were to die
  • within 6 months.
  • 4. If the physician is uncertain about the surprise question, the patient is
  • eligible if presenting with at least one SPICT indicator
  • Relatives of participating patients are eligible to participate in the study if
  • they are 18 years or older and provide informed consent to participate, and if
  • the patient agrees. Relatives can be a family member, friend or other close
  • relative. They have to be aware that the patient is unlikely to recover from
  • his/her disease.

排除标准

  • 1.The patient is incapable of filling in a questionnaire in the country*s main
  • language or in English (patients may be supported by relatives when filling in
  • the questionnaire).
  • 2. The patient is incapable of providing informed consent to participate in the
  • study, as assessed by the attending physician.
  • Relatives are not eligible if they are incapable of filling in a questionnaire
  • in the country*s main language or in English.

研究者

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