Assessment of Cardiopumonary Resuscitation (CPR) Competency Post ALS Course

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorNational Hepatology & Tropical Medicine Research Institute

About this trial

to assess chest compression competency in healthcare providers following ALS training to identify areas for improvement and ensure high-quality CPR delivery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Providers who will complete an ALS training course (two day-course).

Disqualifiers

Providers who will not complete ALS training course, those with physical limitations preventing effective chest compressions. Providers who will take immediate life support course (one day course), candidates attend from other courses to attend missed session and candidates who arrive late and cannot join the pre-course assessment.

Trial design

Design model

Single group

Treatments tested in this trial

  • Education (ALS provider course) in Egypt

    Other intervention

    Participants complete an ALS course, including theoretical and practical components focused on scenario based simulations for CPR and chest compressions.

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: CPR competency pre and post ALS CourseOther 1 intervention

Trial outcomes

Primary outcomes

1

The primary outcome is to assess CPR competency between ALS providers at the end of the ALS course if they will achieve the standard cutoff values and score.

CCF%

Time frame
two day course
2

The primary outcome is to assess CPR competency between ALS providers at the end of the ALS course if they will achieve the standard cutoff values and score.

Chest compression depth %

Time frame
Two day course

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.