NCT05312931

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started May 2022

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 17, 2022

Completed
2 months until next milestone

First Posted

Study publicly available on registry

April 6, 2022

Completed
25 days until next milestone

Study Start

First participant enrolled

May 1, 2022

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2023

Completed
Last Updated

April 6, 2022

Status Verified

March 1, 2022

Enrollment Period

12 months

First QC Date

February 17, 2022

Last Update Submit

March 28, 2022

Conditions

Keywords

retention of knowledgeretention of skillsFirst Aid

Outcome Measures

Primary Outcomes (6)

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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 Outcomes (5)

  • Comparison of group A and B: Chest compressions/ventilation ratio

    up to 36 months

  • Comparison of group A and B: Depth of chest compressions

    up to 36 months

  • Comparison of group A and B: Frequency of chest compression

    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: rescue breaths

    up to 36 months

Study Arms (2)

Group A

students who underwent original concept of First Aid

Other: OSCE

Group B

student who underwent new concept of First Aid

Other: OSCE

Interventions

OSCEOTHER

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

Group AGroup B

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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.

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Martina Kosinová, MD

    Masaryk University Faculty of Medicine

    STUDY CHAIR

Central Study Contacts

Tereza Prokopová, MD

CONTACT

Tereza Vafková, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

February 17, 2022

First Posted

April 6, 2022

Study Start

May 1, 2022

Primary Completion

April 30, 2023

Study Completion

April 30, 2023

Last Updated

April 6, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will not share

The investigators do not plan to share IPD.