Skip to main content
Clinical Trials/NCT05312931
NCT05312931
Unknown
Not Applicable

Retention of Knowledge and Skills of First Aid After Change in Concept of Teaching First Aid

Brno University Hospital0 sites30 target enrollmentMay 1, 2022
ConditionsFirst Aid

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
First Aid
Sponsor
Brno University Hospital
Enrollment
30
Primary Endpoint
Measurement of CPR quality - frequency of chest compressions
Last Updated
4 years ago

Overview

Brief Summary

The investigators will evaluate the effect of simulation-based education in First Aid practice on knowledge and skills retention.

Detailed Description

In autumn semester 2020 a new concept of the subject First aid for the students of General medicine and Dentistry at Faculty of Medicine of Masaryk University was introduced. This concept based on evidence-based medical education puts different principles such as simulation-based education, learner-centred learning, peer learning and outcome-based education into practice. First aid training (FAT) is indispensable part of the curriculum and knowledge of the first year medical students. The investigator´s aim is to evaluate if the new concept of the first aid training led to improvement in knowledge and mainly in skills of the students. Investigator´s null hypothesis is that the new concept does not lead to improvement in the long-term retention of the knowledge and the skills than the original concept. The investigators will compare tested knowledge and skills of the students who underwent FAT in autumn semester 2019 (original concept, group A) and the students who underwent FAT in autumn semester 2020 (new concept, group B). The evaluation of the two groups will happen in the interval of 20-24 months after the completion of the FAT. Group A will be evaluated in autumn semester 2021, group B in autumn semester 2022. The evaluation method will be based on a knowledge test and a OSCE (objective structured clinical examination) stations. Applying principles of evidence-based medical education into practice and designing FAT according to simulation-based education could lead better long-term retention of knowledge and skills of the students.

Registry
clinicaltrials.gov
Start Date
May 1, 2022
End Date
April 30, 2023
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Brno University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Tereza Prokopova, MD

Principal investigator

Brno University Hospital

Eligibility Criteria

Inclusion Criteria

  • Students of General medicine and Dentistry of the Faculty of Medicine of Masaryk University who underwent FAT in autumn semester 2020 and 2021 and have not been involved in Student as Teacher programme.

Exclusion Criteria

  • Students of General medicine and Dentistry of the Faculty of Medicine of Masaryk University who underwent FAT in different time intervals or who underwent FAT in autumn semester 2020 and 2021 and also have been involved in Student as Teacher programme.

Outcomes

Primary Outcomes

Measurement of CPR quality - frequency of chest compressions

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: frequency of chest compressions (compressions/min) in 2 min CPR will be measured with qCPR software. Method of mesurement: (qCPR Anne - compression/ventilation feedback software).

Measurement of CPR quality - chest compression/ventilation ratio

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: chest compression/ventilation ratio - investigator will count the number of chest compressions and a number of ventilation in each cycle in 2 min CPR. It will be statistically analyzed.

Measurement of CPR quality - percentage of adequate depth of chest compressions

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: percentage of adequate depth of chest compressions (%) in 2 min CPR. Adequate depth of chest compression (5 - 6 cm). Method of mesurement: (qCPR Anne - compression/ventilation feedback software).

Measurement of CPR quality - rescue breaths

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: the number of detectable rescue breaths and number of unsuccessful rescue breaths during 2 min in CPR will be recorded. Detectable rescue breath means that the software was able to detect the rescue breath. Unsuccessful rescue breath means that the student tried to deliver rescue breath but the software was not able to detect it. Method of mesurement: (qCPR Anne - compression/ventilation feedback software).

Measurement of CPR quality - the longest pause in chest compressions (s)

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: the longest pause in chest compressions (s) in 2 min CPR. Method of mesurement: (qCPR Anne - compression/ventilation feedback software).

Measurement of CPR quality - percentage of chest compression when thorax was adequately released

Time Frame: Up to 36 months

CPR quality will be measured with CPR monitoring (qCPR Anne - compression/ventilation feedback software). Attributes of CPR and a method of measurement: percentage of chest compression when thorax was adequately released (%) in 2 min CPR. Method of mesurement: (qCPR Anne - compression/ventilation feedback software).

Secondary Outcomes

  • Comparison of group A and B: Depth of chest compressions(up to 36 months)
  • Comparison of group A and B: The longest pause in chest compressions(up to 36 months)
  • Comparison of group A and B: Chest compressions/ventilation ratio(up to 36 months)
  • Comparison of group A and B: Frequency of chest compression(up to 36 months)
  • Comparison of group A and B: rescue breaths(up to 36 months)

Similar Trials