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临床试验/NCT03234049
NCT03234049已完成不适用

The Use of a Pediatric Trauma Checklist to Improve Clinical Performance in a Simulated Trauma Resuscitation: a Randomized Trial

KidSIM Simulation Program1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2016年11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
已完成
发起方
入组人数
56
试验地点
1
主要终点
Time measurement interval to initiation of bag mask ventilation

研究概览

简要总结

The use of a pre-arrival and pre-departure trauma checklist to optimize care has not yet been studied. The Alberta Children's Hospital (ACH) Trauma Checklist was developed by the ACH Resuscitation Council with input from the ACH Trauma Program. The purpose of this study is to determine if the introduction of the ACH Trauma Checklist as a cognitive aid, coupled with an educational session, will improve clinical performance in a simulated environment. The investigators plan to conduct a pilot, randomized control trial assessing the impact of the ACH trauma checklist on time to critical interventions on a simulated pediatric patient by multidisciplinary teams. The investigators hypothesize that teams who use a trauma checklist as a cognitive aid will have faster initiation of key clinical interventions within a simulated pediatric trauma resuscitation. Improvements in performance in a simulated environment with this tool may translate to similar results in the clinical setting.

详细描述

Research Aims:

Aim 1: To evaluate the effectiveness of a pre-arrival, pre-departure trauma checklist on improving time to initiation of key clinical interventions in a simulated pediatric trauma scenario

Aim 2: To evaluate the impact of a pre-arrival, pre-departure trauma checklist on completion of primary and secondary survey tasks as demonstrated by an Advanced Trauma Life Support (ATLS) performance tool.

Aim 3: To evaluate the cognitive task load of a trauma checklist on emergency department physicians during a simulated trauma resuscitation scenario.

Aim 4: To describe patterns of eye movement of a trauma team leader in a simulated scenario in relation to critical patient interventions and team communication.

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
None

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Trauma team leader inclusion criteria:
  • •Pediatric emergency medicine physician
  • •Second physician inclusion criteria:
  • •Pediatric emergency medicine physician
  • •Nurse inclusion criteria:
  • •Pediatric emergency registered nurse

排除标准

  • •Previous participation in the study

研究组 & 干预措施

Control Arm

No Intervention

In the control arm, teams will not receive a copy of the checklist for use.

Checklist Arm

Experimental

In the intervention arm, the participants will watch a 10 minute recorded educational video demonstrating the use of the trauma checklist prior to their simulation scenario. These teams will subsequently receive a copy of the checklist for use during their simulation scenario.

干预措施: Checklist (Other)

结局指标

主要结局

Time measurement interval to initiation of bag mask ventilation

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to first assisted bag mask breath

Time measurement interval to initiation of endotracheal tube placement

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to endotracheal tube placement

Time measurement interval to initiation of paralytic medication

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to delivery of intubation paralytic medication

Time measurement interval to application of pelvic binder

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to application of pelvic binder

Time measurement interval to initiation of induction medication

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to delivery of intubation induction medication

Time measurement interval to initiation of fluid bolus administration

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to initiation of first crystalloid fluid bolus

Time measurement interval to completion of log roll

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to completion of patient log roll

Time measurement interval to initiation of blood product administration

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to initiation of first blood product administration

Time measurement interval to Glasgow Coma Score calculation

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to first verbalized and calculated Glasgow Coma Score

Time measurement interval to initiation of hyperosmolar therapy

时间窗: within the 20 minute simulation scenario

Interval from start of scenario to initiation of hyperosmolar therapy, either mannitol or 3% saline

次要结局

  • Eye movements of the trauma team leader(within the 20 minute simulation scenario)
  • Advanced Trauma Life Support Task Performance(within the 20 minute simulation scenario)
  • Checklist completion(within the 20 minute simulation scenario)

研究者

发起方
KidSIM Simulation Program
申办方类型
Network
责任方
Sponsor

研究点 (1)

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