跳至主要内容
临床试验/NCT04926610
NCT04926610Enrolling By Invitation不适用

The Effect of Proactive Clinical Ethics Consultations on End-of-life Care of the Critically Ill in the Intensive Care Settings

Kaohsiung Medical University Chung-Ho Memorial Hospital2 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2014年4月7日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
224
试验地点
2
主要终点
ICU length of stay

研究概览

简要总结

Study objective: This study is planning to explore factors predicting the use of life-sustaining treatment, develop the screening criteria of proactive clinical ethics consultations, the effect of proactive clinical ethics consultations and interprofessional practice on end-of-life care of the critically ill in the intensive care settings, and develop the competency for trainees by interprofessional education.

Methods: Data will be collected prospectively. Data between January 2013 and April 2014 was collected from hospital electronic record and ethics consultation document. All data will be analyzed for patients dying in the intensive care settings during the first stage of the study. Factors predicting the use of life-sustaining treatment will be determined. The Delphi technique will be applied to secure a consensus among the panel of experts chosen to help develop the screening criteria of proactive ethics consultations. A prospective randomized controlled trial will be conducted during the second stage of the study on a convenience sample of adult critical ill patients in the intensive care settings. Patients will randomize to the intervention group receive proactive ethics consultations. The control group will undergo routine intensive care, receiving clinical ethics consultations as requested by healthcare team, patients or family. All participants will be asked to complete a questionnaire rating their satisfaction with the healthcare process and consultations if conducted. Mean length of stay and the duration of the use of life-sustaining treatment will be compared between two groups. Secondary outcomes will include the proportion of satisfied families and healthcare team members. The interprofessional education with the core curriculum and case scenario for simulation will be developed, implement, and evaluated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Medical staff involved in caring for terminal patients
  • Cases of active clinical ethics consultation in our hospital

排除标准

  • Medical staff who refuse to participate in the study or are unable to understand the way the study is conducted
  • Cases of refusing to participate in the research or unable to understand the way the research is conducted.

结局指标

主要结局

ICU length of stay

时间窗: through study completion, an average of 2 years

days that patient in the intensive care unit

hospital length of stay

时间窗: through study completion, an average of 2 years

days that patient in the hospital

use of life-sustaining treatment

时间窗: through study completion, an average of 2 years

days of the use of life-sustaining treatment

次要结局

  • healthcare provider satisfaction questionnaire(within 2 weeks after patient discharge)
  • family or surrogate satisfaction questionnaire(within 4 weeks after patient discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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