Development and Validation of a Regional Multi-scale System for the Prediction of the Patient Flow in the Emergencies and the Need for Hospitalization (PRED-URG)
2022年3月21日 更新者:Assistance Publique - Hôpitaux de Paris
Development and Validation of a Regional Multi-scale System in Ile-de-France for the Prediction of the Patient Flow in the Emergency Department and the Need for Hospitalization
The main objective of this retrospective study is to validate a prediction system of emergencies department (ED) attendance on a wide range of time and the need for hospitalization, at various levels of perimeter (with all emergency departments or one ED in particular), with all patients or with one sub-group of patients (age, gravity, care).
研究概览
详细说明
As secondary objectives, the study aims:
- to measure the influence of different factors as environmental or structural and to identify the modifiable factors, then to allow us to test by simulation, impact of various interventions (for example: opening of hospitals and reinforcement of ED teams) on arrival flows or regenerated tension inside ED teams.
- to study the relation between the flows (arrival patients, hospitalized patients) and the time of ED visit or the indicators of tension of ED team.
- Typology of ED in the region of Paris permitting afterward comparison the benchmarking type between similar structures.
This retrospective study will be performed on database: individual data in the region of Paris of summation of ED visits and data on the structures of health cares, as well as environmental data (principal given cares, weather, moves, circulations, pollution, strikes, vacations, etc.)
研究类型
观察性的
注册 (预期的)
18000000
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Mathias WARGON, MD
- 电话号码:+33 1 49 83 10 86
- 邮箱:m.wargon@ch-bry.org
学习地点
-
-
Val-de-Marne
-
Bry sur Marne、Val-de-Marne、法国、94360
- 招聘中
- Emergency Department - Bry sur Marne Hospital
-
接触:
- Mathias WARGON, MD
- 电话号码:+33 1 49 83 10 86
- 邮箱:m.wargon@ch-bry.org
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Adults or children who have been recorded as patients in emergency departments between 2010 and 2015 are all eligibles with unlimited number of care.
85 Health Facilities in Ile de France who have emergency departments will participate the study.
描述
Inclusion Criteria:
- All subjects have been recorded as patients in emergency departments between 2010 and 2015.
Exclusion Criteria:
- None
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
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 |
---|---|---|
Prediction of emergency department visits
大体时间:throughout the study, an average of 18 months
|
Calculated base on regional database: individual data of summation of ED visits in the region of Paris and structural data of health cares
|
throughout the study, an average of 18 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Prediction by age
大体时间:throughout the study, an average of 18 months
|
By sub-group of child or senior
|
throughout the study, an average of 18 months
|
Prediction by lever of gravity
大体时间:throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Prediction by type of care
大体时间:throughout the study, an average of 18 months
|
By type : (medical, surgical or intensive) care
|
throughout the study, an average of 18 months
|
Prediction by need of hospitalization or no
大体时间:throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Relation between flow of patients and indicator of tension of team
大体时间:throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Relation between flow of patients and time of ED visit
大体时间:throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
Typology of ED of the region of Paris
大体时间:throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Mathias WARGON, MD、Emergency Department - Bry sur Marne Hospital
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年6月1日
初级完成 (预期的)
2023年12月1日
研究完成 (预期的)
2023年12月1日
研究注册日期
首次提交
2017年2月6日
首先提交符合 QC 标准的
2017年2月9日
首次发布 (实际的)
2017年2月14日
研究记录更新
最后更新发布 (实际的)
2022年3月22日
上次提交的符合 QC 标准的更新
2022年3月21日
最后验证
2022年3月1日
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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