The Efficacy of Simulation Manikins in the Military Medics Training

Sponsor
Czech Technical University in Prague (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05612828
Collaborator
Military University Hospital, Prague (Other)
50
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Study Details

Study Description

Brief Summary

The aim of the study is to verify the applicability of simulation manikin in combat training of military medics. The research will be conducted on healthy volunteers - medics of the Czech Armed Forces, as a part of the compulsory medical courses required for foreign military missions as a "Combat Life Saver". Comparison of the performance of two groups of course participants who were trained using the standard approach versus experiential learning using simulation manikins.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Conventional versus simulation manikin training
N/A

Detailed Description

With the development of modern hi-tech manikins and their growing popularity in the training of "civilian" medics, the possibilities of their application in the training of military medics are emerging. The aim of the study is to verify the applicability of simulation manikin in combat training of military medics. The research will be conducted on healthy volunteers - medics of the Czech Armed Forces, as a part of the compulsory medical courses required for foreign military missions as a "Combat Life Saver". Comparison of the performance of two groups of course participants who were trained using the standard approach versus experiential learning using simulation manikins. In addition to monitoring the particular professional performance of the trainees, changes in basic physiological functions, including the endocrinological response to stress conditions, will be evaluated.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized control trialrandomized control trial
Masking:
Double (Participant, Investigator)
Primary Purpose:
Health Services Research
Official Title:
The Efficacy of Simulation Manikins in the Military Medics Training
Actual Study Start Date :
Nov 7, 2022
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Conventional training

Combat Life Savers trained by conventional combat medicine approach.

Behavioral: Conventional versus simulation manikin training
Two approaches to training Combat Life Savers will be employed and performance of participants will be evaluated.

Experimental: Simulation manikin training

Training based on principles of simulation medicine.

Behavioral: Conventional versus simulation manikin training
Two approaches to training Combat Life Savers will be employed and performance of participants will be evaluated.

Outcome Measures

Primary Outcome Measures

  1. Duration time of the of use of tourniquet [10 minutes]

    Time to complete diagnostics and treatment of bleeding (in seconds)

  2. Correctness of treatment of severe bleeding [10 minutes]

    Based on standardized forms (points on a standardised scale)

  3. Duration time of the of use of nasal airway [10 minutes]

    Time to complete diagnostics and treatment of airway obstruction (in seconds)

  4. Correctness of treatment of airway obstruction [10 minutes]

    Based on standardized forms (points on a standardised scale)

  5. Duration time of the use of chest seal [10 minutes]

    Time to complete diagnostics and treatment of open pneumothorax (in seconds)

  6. Correctness of treatment of open pneumothorax [10 minutes]

    Based on standardized forms (points on a standardised scale)

Secondary Outcome Measures

  1. Stress level 1 [1 hour]

    Level of stress response based on changes in blood pressure (in mm of mercury)

  2. Stress level 2 [1 hour]

    Level of stress response based on changes in heart rate (in beats per minute)

  3. Stress level 3 [1 hour]

    Level of stress response based on changes in cortisol level (in nmol/L)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • active soldier during the Tactical Combat Casualty Care course
Exclusion Criteria:
  • not willing to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Czech Technical University in Prague Kladno Czechia 27201

Sponsors and Collaborators

  • Czech Technical University in Prague
  • Military University Hospital, Prague

Investigators

  • Study Director: Karel RoubĂ­k, Ph.D., Czech Technical University in Prague

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Czech Technical University in Prague
ClinicalTrials.gov Identifier:
NCT05612828
Other Study ID Numbers:
  • VentRes-2022-01-JP
First Posted:
Nov 10, 2022
Last Update Posted:
Dec 13, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Czech Technical University in Prague
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 13, 2022