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临床试验/NCT03995095
NCT03995095已完成不适用

Intervention in Spirituality at the End of Life. The Kibo Protocol

University of Valencia2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Change in the dimension of spirituality (PRE and POST measures)

研究概览

简要总结

This work aims to study the benefits that the therapeutic interview Kibo in palliative care patients can have for spirituality.

A parallel randomized controlled trial of two groups was performed. Information was collected on 60 palliative care patients during the moments before and after the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

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

  • To be 18 or more years of age.
  • Being in advanced or terminal disease phase (following World Health Organization criteria).
  • To have preserved cognitive capacity.
  • To have signed the informed consent.

排除标准

  • a) Estimated time of survival: Patients with a life expectancy of two weeks or less will not be intervened.

结局指标

主要结局

Change in the dimension of spirituality (PRE and POST measures)

时间窗: Baseline up to 4 weeks

This variable was assessed with the Spirituality questionnaire from the Spanish Society of Palliative Care (SECPAL). This questionnaire contains 8 items, and it provides scores from 0 to 32, where higher values represent a better outcome. In order to observe the change in the dimension of spirituality, it was measured at in two time points: First measurement: PRE. Once the participant had signed the informed consent, the initial score for this outcome was assessed. Second measurement: POST. Up to 4 weeks after the first measurement, the second measurement of the same variable was carried out. Between first and second measurement, the control group received the usual psychological attention, whereas the intervention group received usual psychological attention plus attention of spiritual needs following the Kibo protocol (intervention).

次要结局

  • Change in resilience (PRE and POST measures)(Baseline up to 4 weeks)
  • Change in demoralization (PRE and POST measures)(Baseline up to 4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

M. Antonia Pérez-Marín

Profesora Titular

University of Valencia

研究点 (2)

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