跳至主要内容
临床试验/NL-OMON26073
NL-OMON26073尚未招募不适用

Attempts to CONTrol the END of life in people with dementia - Work Package 1.

eiden University Medical Center, Leiden, The Netherlands0 个研究点目标入组 900 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
尚未招募
发起方
入组人数
900

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

入选标准

  • The person with dementia:
  • has a diagnosis of irreversible dementia established by a physician
  • has been informed about and is aware of his or her diagnosis
  • has a family caregiver (spouse, friend, partner, daughter/son, etc.) who is willing to participate in the study
  • has decision making capacity and is able to communicate through sufficient memory and language
  • has sufficient capacity of the local or English language to participate in the interview
  • is able to understand and sign the consent form
  • has adequate vision and hearing (can be achieved by using corrective lenses and hearing aid if required)
  • consents to participate.
  • The family caregiver:
  • is willing and able to participate in the study
  • the person with dementia they care for is willing and able to participate
  • is at least 18 years old
  • has sufficient capacity of the local or English language to participate in the interview
  • consents to participate.
  • The physician:
  • practices a specialty that includes provision of end-of-life care for individuals living with dementia (depending on the country, the specialty could be primary care physicians such as general practitioners and elderly care physicians, geriatricians, geriatric psychiatrist, neurologists)
  • is willing and able to participate in the study
  • consents to participate.

排除标准

  • The person with dementia is currently affected by a severe psychiatric disorder (e.g., major depression, schizophrenia, substance abuse, PTSD) as diagnosed by a psychiatrist, psychologist, or physician.
  • The person is expected to die in a few weeks.

研究者

发起方
eiden University Medical Center, Leiden, The Netherlands

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