Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05312931
Other study ID # ReFA
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2022
Est. completion date April 30, 2023

Study information

Verified date March 2022
Source Brno University Hospital
Contact Tereza Prokopová, MD
Phone +420736669784
Email prokopova.tereza@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


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 investigatorĀ“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. InvestigatorĀ“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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date April 30, 2023
Est. primary completion date April 30, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
OSCE
Students undergo OSCE (objective structured clinical exams). It means students will perform CPR for 2 min and their success rate will be monitored.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Brno University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of CPR quality - chest compression/ventilation ratio 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.
Up to 36 months
Primary Measurement of CPR quality - percentage of adequate depth of chest compressions 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).
Up to 36 months
Primary Measurement of CPR quality - the longest pause in chest compressions (s) 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).
Up to 36 months
Primary Measurement of CPR quality - percentage of chest compression when thorax was adequately released 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).
Up to 36 months
Primary Measurement of CPR quality - rescue breaths 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).
Up to 36 months
Primary Measurement of CPR quality - frequency of chest compressions 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).
Up to 36 months
Secondary Comparison of group A and B: Chest compressions/ventilation ratio Statistic analysis will be used in a comparison of Chest compressions/ventilation ratio in groups A and B.
Chest compressions/ventilation ratio - good ratio 30:2 according to ERC.
up to 36 months
Secondary Comparison of group A and B: Depth of chest compressions Statistic analysis will be used to compare the depth of chest compressions in groups A and B.
Depth of chest compressions: adequate chest compression is 5-6 cm.
up to 36 months
Secondary Comparison of group A and B: Frequency of chest compression Statistic analysis will be used in a comparison of the frequency of chest compression in groups A and B.
Frequency of chest compression: adequate average frequency is 100-120/min.
up to 36 months
Secondary Comparison of group A and B: The longest pause in chest compressions Statistic analysis will be used in a comparison of the longest pause in chest compressions in groups A and B.
The longest pause in chest compressions: adequate is up to 10s.
up to 36 months
Secondary Comparison of group A and B: rescue breaths Statistic analysis will be used in a comparison of the longest pause in chest compressions in groups A and B.
The number of detectable rescue breaths and number of unsuccessful rescue breaths during 2 min in CPR will be statistically analyzed.
up to 36 months
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04914871 - Readiness for Basic Life Support in Schools N/A
Active, not recruiting NCT06279702 - Serious Game Simulation and Comics in School Students N/A
Completed NCT06000878 - Evaluate the Effectiveness of First Aid E-book Intervention Among New Nurses N/A
Enrolling by invitation NCT06169839 - The Effect of Different Simulation Methods Used in Adult Basic Life Support Training N/A
Not yet recruiting NCT03191279 - First Aid by Laypersons - Effect on Mortality and Length of Stay N/A
Completed NCT06155149 - Effects of the Mobile Application Developed for Families After the Earthquake on First Aid Knowledge and Burn Prevention N/A