The Comparison of the Two Simulators for ACLS Training

August 5, 2021 updated by: Guolin Wang, Tianjin Medical University General Hospital

The Comparison of the Two Simulators for ACLS Straining:Does the Computer Simulator Have the Same Effectiveness as the Mannequin Simulato

Compared two different training simulators(the computer screen-based simulator versus the full-scale mannequin-based simulator) with respect to training effectiveness in ACLS training.At the same time,evaluate the effectiveness of combination of these two simulators(screen-based simulation followed by mannequin-based simulation),so that to find out a new simulation format for ACLS training.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

A prospective,single-blinded,randomized controlled study was used.30 first-year residents were randomized to Computer screen-based simulator group(C group),full scale Mannequin-based group(M group) and screen+Mannequin combing group(SM group).After a 30min ACLS lecture and 30min integrated CPR hands-on training,all groups received a pretest.The C group was exposed to two ACLS computer scenarions,M group was exposed to two ACLS mannequin scenario.Each scenario took 10min and followed by 20min debriefing with simulation educator.After the training session,each participant completed by modified'megacode'checklist.

Study Type

Interventional

Enrollment (Anticipated)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • China
    • Tianjin
      • Tianjin, Tianjin, China
        • Enrolling by invitation
        • the Computer Simulator,the Mannequin Simulator
      • Tianjin, Tianjin, China
        • Recruiting
        • the Computer Simulator,the Mannequin Simulator
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

- training doctors,intern Exclusion Criteria:Standardized training of doctors，Medical students

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: OTHER
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
OTHER: computer simulator
training students ACLS by one computer simulator
Other: computer simulator and mannequin simulator
compared two different training simulators with respect to training effectiveness in ACLS training.
OTHER: mannequin simulator
training students ACLS by one mannequin simulator
Other: computer simulator and mannequin simulator
compared two different training simulators with respect to training effectiveness in ACLS training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the effection of the two different simulators for ACLS training.
Time Frame: six months
If all the groups have improvement in konwledge,ACLS and non-technical skills.Compared with C group,M group，the scores of each group were compared
six months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Tianjin Medical University General Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 4, 2021

Primary Completion (ANTICIPATED)

December 31, 2021

Study Completion (ANTICIPATED)

December 31, 2021

Study Registration Dates

First Submitted

June 23, 2021

First Submitted That Met QC Criteria

August 5, 2021

First Posted (ACTUAL)

August 12, 2021

Study Record Updates

Last Update Posted (ACTUAL)

August 12, 2021

Last Update Submitted That Met QC Criteria

August 5, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • GWang

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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