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临床试验/NCT02365792
NCT02365792撤回不适用

Efficacy of a Clinical Decision Support System in Prehospital Care: Single Blind, Randomized Clinical Trial.

KU Leuven1 个研究点 分布在 1 个国家开始时间: 2016年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
KU Leuven
试验地点
1
主要终点
Treatment protocol adherence

研究概览

简要总结

The ProDEms-trial focuses on nurses and ambulance drivers working in prehospital care, taking care on the one hand of patients suffering from time-sensitive critical conditions like STEMI, acute stroke or severe traumatic brain injury, and on the other hand of patients whose lives are not in immediate danger but suffer from acute exacerbation of chronic conditions or suffer from acute pain.

In the current study the investigators will use a multistage approach to test the hypothesis whether the use of a CDSS in prehospital emergency care will: 1. Improve protocol adherence, 2. Reduce emergency department length of stay, 3. Improves diagnostic accuracy; without impeding the workflow of the prehospital team or impairing patient safety.

研究设计

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

入排标准

年龄范围
1 Year 至 112 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients who receive treatment from the Paramedic Intervention Team (PIT) in the prehospital Emergency Medical Services (EMS) area of the University Hospitals, Leuven.

排除标准

  • •Patient-related interventions not dispatched by the Emergency Medical Dispatch center (EMD)
  • •Patient related interventions during transport between two healthcare facilities or in mass casualty situations.

研究组 & 干预措施

CDSS1

Active Comparator

The CDSS1 will provide decision support according to existing protocols for clinical procedures and medical treatment, mainly starting from specific symptoms or diagnostic related patients groups. The symptom oriented approach is categorised in a specific list of predetermined conditions.

干预措施: Clinical Decision Support Tool for Prehospital Care (Procedure)

CDSS2

Active Comparator

The CDSS2 will provide decision support according to existing protocols for clinical procedures and medical treatment, mainly starting from specific symptoms or diagnostic related patients groups. The symptom oriented approach is categorised in a specific list of predetermined conditions.

干预措施: Clinical Decision Support Tool for Prehospital Care (Procedure)

Booklet

Placebo Comparator

The control group will provide prehospital patient care with usual decision support: a pocket-size booklet, backed by a mobile phone through which the PIT can get in contact with an Emergency Physician.

干预措施: Clinical Decision Support Tool for Prehospital Care (Procedure)

结局指标

主要结局

Treatment protocol adherence

时间窗: Up to 12 months

Measured by comparing the prescribed actions to be taken following the selected standing order (-s) or procedures, with the actual action (-s) taken.

次要结局

  • Consistency in reported diagnose and the choice of PIT standing order (-s) or procedure (-s)(Up to 12 months)
  • Alignment between diagnostic accuracy and interventions taken.(Up to 12 months)
  • Length of Stay in the ED(Up to 12 months)
  • Prehospital Patient Time Interval(Up to 12 months)

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Olivier Hoogmartens

Head of the Academic Center for General Practice

KU Leuven

研究点 (1)

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