Critically Ill Patient's Capacity (Capacity)
研究概览
详细说明
After written information and consent, an independent, specially trained investigator interviews patients with a standardised test.
After written information and consent, an independent, specially trained investigator interviews residents, doctors and nurses in charge of the patient and ask them how they rates patients capacity.
研究类型
注册 (实际的)
联系人和位置
学习地点
-
-
-
Clermont-Ferrand、法国、63003
- CHU clermont-ferrand
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Caregivers :
Doctors, hospital interns, nurses state of both sexes, aged 18 years or more working in Intensive Care, members of a social security system engaged in a clinic on the day of the assessment
- Patients :
Patients of both sexes, aged 18 years or more hospitalized in Intensive Care, members of a social security system
Exclusion Criteria:
-
学习计划
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
Decision making
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
correlation between the decision-making capacity and the decision-making capacity assessed by standardized methods
大体时间：at day 1
|
standardized methods (patient has decision-making capacity yes/no) as described by Sessums LL, Zembrzuska H, Jackson JL.
Does this patient have medical decision-making capacity?
JAMA.
2011;306(4):420-427. doi:10.1001/jama.2011.1023.
|
at day 1
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
correlation between the global decision-making capacity evaluated by the physician in charge of the patient and the specific decision-making capacity assessed by physician in charge of the patient
大体时间：at day 1
|
Ability to designate a person of confidence, capacity to consent to inclusion in a research protocol, ability to participate in a discussion on the limitation therapy
|
at day 1
|
|
association between burnout in evaluators and consistency of their decision-making capacity assessments
大体时间：at day 1
|
at day 1
|
|
|
Correlation between the decision-making capacity evaluated by the physician in charge of the patient, the nurse in charge of the patient and a physician not in charge of the patient
大体时间：at day 1
|
at day 1
|
合作者和调查者
调查人员
- 首席研究员：Alexandre Lautrette、University Hospital, Clermont-Ferrand
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.