War-Related Injuries Clinical Trial
Official title:
The Efficacy of Simulation Manikins in the Military Medics Training
Verified date | February 2024 |
Source | Czech Technical University in Prague |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Enrolling by invitation |
Enrollment | 50 |
Est. completion date | December 31, 2026 |
Est. primary completion date | December 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - active soldier during the Tactical Combat Casualty Care course Exclusion Criteria: - not willing to participate |
Country | Name | City | State |
---|---|---|---|
Czechia | Czech Technical University in Prague | Kladno |
Lead Sponsor | Collaborator |
---|---|
Czech Technical University in Prague | Military University Hospital, Prague |
Czechia,
McCarthy M. US military revamps combat medic training and care. Lancet. 2003 Feb 8;361(9356):494-5. doi: 10.1016/S0140-6736(03)12494-4. No abstract available. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration time of the of use of tourniquet | Time to complete diagnostics and treatment of bleeding (in seconds) | 10 minutes | |
Primary | Correctness of treatment of severe bleeding | Based on standardized forms (points on a standardised scale) | 10 minutes | |
Primary | Duration time of the of use of nasal airway | Time to complete diagnostics and treatment of airway obstruction (in seconds) | 10 minutes | |
Primary | Correctness of treatment of airway obstruction | Based on standardized forms (points on a standardised scale) | 10 minutes | |
Primary | Duration time of the use of chest seal | Time to complete diagnostics and treatment of open pneumothorax (in seconds) | 10 minutes | |
Primary | Correctness of treatment of open pneumothorax | Based on standardized forms (points on a standardised scale) | 10 minutes | |
Secondary | Stress level 1 | Level of stress response based on changes in blood pressure (in mm of mercury) | 1 hour | |
Secondary | Stress level 2 | Level of stress response based on changes in heart rate (in beats per minute) | 1 hour | |
Secondary | Stress level 3 | Level of stress response based on changes in cortisol level (in nmol/L) | 1 hour |
Status | Clinical Trial | Phase | |
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