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