The Trial of Emergency Medicine Protocols In Simulation Sraining (TEMPIST) study

Not Applicable

Recruiting

• Conditions: Resuscitation; Public Health - Health service research; Injuries and Accidents - Other injuries and accidents

• Registration Number: ACTRN12616001456448
• Lead Sponsor: niversity Centre for Rural Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-10-18
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Doctors and Nurses from the Local Health District who are already attending resuscitation training courses at the UCRH or volunteer to participate in their own time. It is anticipated that groups will vary in their preexisting skill level and level of experience.

* Recruited staff will need to have worked within an Australian Emergency Department within the last 12 months.
* Age 18 or above.

Exclusion Criteria

* Nursing and Medical Students will be excluded from the trial.
Study personnel will be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
There are 4 scenarios. .Each scenario will be recorded on video and the primary outcome measures will be a list of 15 predetermined tasks that are expected to be completed within the 15 minute time frame. Thus across four scenarios, each team will be measured on a total of 60 key processes for adherence (yes or no) with half the processes for a given team with the handbook available. Two clinicians will observe the video recorded data and rate whether the group has performed the required tasks. [After completing all four simulation training scenarios.]

Secondary Outcome Measures

Name	Time	Method
Completion of the questionnaire specifically designed for this study. The composite secondary outcome measure will look at the quality and usefulness of the sessions. These will be scored on a five-point Likert scale. [After completing all four simulation training scenarios.];Completion of the questionnaire specifically designed for this study. The composite secondary outcome measure will look at the quality and usefulness of the protocols These will be scored on a five-point Likert scale. [After completing all four simulation training scenarios.]