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临床试验/ChiCTR2500113083
ChiCTR2500113083尚未招募Unknown

An evidence-based advance care planning programme to promote end-of-life care planning among patients with advanced diseases in the Emergency Department – a feasibility randomised controlled trial

未提供1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年11月24日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Recruitment and retention rate

研究概览

简要总结

The study aims to examine the feasibility and acceptability of an evidence-based ACP programme among patients with advanced diseases in the Emergency Department. The objectives of the study are to determine the feasibility of conducting an ACP programme in the ED based on recruitment and attrition rate, to examine the acceptability of the intervention based on satisfaction survey and qualitative comments on patient’s experiences, and to examine the preliminary effect of the programme on patient reported ACP readiness and evidence of ACP documentation on medical record.

研究设计

研究类型
Interventional
主要目的
随机平行对照
盲法
None

入排标准

年龄范围
18 至 —(—)
性别
All

入选标准

  • Subjects will be recruited from Emergency Medicine Wards, ED of two public hospitals in Kowloon West Cluster, Hong Kong. One of the ED is in Kwai Tsing District providing tertiary care while the other ED is located on Lantau Island providing tertiary and rehabilitation service.Participants are adult (18 years old or above) admitted to the EMW, Chinese-speaking, fulfill the two general and one
  • clinical criterion stipulated in the Supportive and Palliative Care Indicator Tools (SPICT™) (The University of Edinburgh,
  • . SPICT was developed as an instrument to identify patients at risk of dying within one year (Paulik et al., 2024).
  • It has a sensitivity of 0.65 (95% CI) and a specificity of 0.72 (95% CI) in detecting life-limiting conditions (Paulik et al.,
  • .By using this dual indicators approach, it allows a more comprehensive and personalized model of care for patients
  • with advanced illnesses (Paulik et al., 2024).

排除标准

  • Patients will be excluded if they are mentally incompetent determined based on the Diagnostic assessment Confusion
  • Assessment Method (3D-CAM) (Marcantonio et al., 2015). The Chinese version of 3D-CAM can be used as a reliable
  • and accurate instrument for delirium assessment, its sensitivity ranges from 85.7 to 100% and the specificity from 95.7
  • to 96.4% (Mu et al., 2020).
  • Patients who were non-Chinese speaking, non-communicable, refusal or unable to give consent, altered sensorium or
  • cognitive functions, physical unwell to receive the intervention, and with previous documented ACP or AMD will be
  • excluded from the study.

研究组 & 干预措施

Experimental Group

Patients in the intervention group will receive a ACP programme which include a six-minute video on introduction toACP, followed by a 30-minute discussion guided by a trained nurse on ACP as well as a pamphlet with written information on the same topic.

Control Group

Patient in the control group will receive usual care such as ward routine and fall prevention advice.

结局指标

主要结局

Recruitment and retention rate

Time spent in each intervention

次要结局

  • ACP engagement
  • Decisional Conflict
  • Documentation of end-of-life care preferences
  • Demographics and health conditions
  • Qualitative Interview

研究者

发起方
未提供

研究点 (1)

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