Standardization of Ambulance Equipment

Safety Issues Clinical Trial

Official title:

The Influence of Standardization of Ambulance Equipment on the Speed of Medical Procedures Provision

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04774900
• Other study ID #: ZZSHMP_002_2021
• Status: Not yet recruiting
• Start date: October 1, 2021
• Est. completion date: December 31, 2021

Study information

• Verified date: August 2021
• Source: Emergency Medical Service, Prague
• Contact: David Peran, Dr.
• Phone: 00420 602 611 746
• Email: David.Peran[@]zzshmp.cz
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of the research is to find out what effect the standardization of ambulance equipment has on the speed of performing specific medical procedures.

Description:

The aim of the research is to find out what effect the standardization of ambulance equipment has on the speed of performing specific medical procedures. In two simulated scenarios, the times from the decision to execution of medical procedures will be measured. In the first scenario, the equipment is located in the standard way and the research participants know where it is located. In the second scenario, the equipment is placed elsewhere and participants do not have the opportunity to check the equipment before the scenario. For the statistical comparison the Student's T-test and Wilcoxon signed-rank test will be used. For analysis of variance will be used the ANOVA test and for more than two dependent selections the Friedman's ANOVA test will be used.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: December 31, 2021
• Est. primary completion date: November 30, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• consent to participate

• times of all procedures recorded

• all procedures provided in a correct way - in meaning of quality of the procedure

Exclusion Criteria:

• disagreement with participation

• not all procedures provided or not provided correctly

Related Conditions & MeSH terms

• Safety Issues

Intervention

Procedure:
• Administration of oxygen
Administration of high-flow oxygen via face mask to a high fidelity mannequin.
• Administration of drug in a nebulizer
Administration of bronchodilator via nebulizer mask to a high fidelity mannequin.
• Securing intravenous line
Securing an intravenous line at the forearm of high fidelity mannequin.
• Administration of IV drug
Administration of bronchodilator via IV line to a high fidelity mannequin.
• Needle decompression of tension pneumothorax
Needle decompression of tension pneumothorax on a high fidelity mannequin.

Locations

Country	Name	City	State
Czechia	Prague Emergency Medical Services	Praha

Sponsors (1)

Lead Sponsor	Collaborator
David Peran

Country where clinical trial is conducted

Czechia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time	Time from decision to execution	Through study completion, an average of 6 months and/or until 100 cases will be collected.