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RecruitingNCT07085832Updated Jul 25, 2025

Assessment of Cardiopumonary Resuscitation (CPR) Competency Post ALS Course

An interventional study of Education (ALS provider course) in Egypt in Chestcompressionadequacy, sponsored by National Hepatology & Tropical Medicine Research Institute. Recruiting at 2 sites in Egypt. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-25.

Sponsored by National Hepatology & Tropical Medicine Research Institute · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Mar 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Jun 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

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

Read the detailed description

Assessment of certain CPR metrics will be done by the following approach;

Pre-course assessment:

Baseline measurement of CPR skills for two minutes cycle using a validated simulator by specialized adult feedback manikins e.g. Prestan CPR Feedback Manikins (i.e. built-in indicators for compression rate and depth), the following metrics will be followed and recorded:

  1. Chest Compression Metrics:

    A. Compression Depth: at least 2 inches (5 cm) for adults, with a maximum of 2.4 inches (6 cm)3.

    B. Compression Rate: 100 to 120 compressions per minute3. C. Release (Recoil): Full chest recoil is essential to allow for effective venous return3.

    D. Hands-off time (Pause): Measured during the simulation, less than 10 seconds3.

    E. Chest Compression Fraction (CCF): Calculated as the ratio of the time spent performing compressions to the total time spent on CPR (including compressions, ventilations, and any pauses). Target will be ≥80%4.

    F. Compression Quality: An overall assessment (percentage shown by the feedback device) of the effectiveness of compressions, which may include depth, rate, and continuity.

  2. Ventilation Metrics:

A. Tidal Volume: Target will be 400-700 mL of air for visible chest rise (in adults)3.

B. Ventilation Rate: 1 breath every 6 seconds (10 breaths per minute during continuous chest compressions for adults)3.

Intervention:

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

Post-course assessment:

Immediate assessment at the end of the second day for CPR competency of 2 minutes cycle using the same simulator and the same parameters assessed pre-course.The scoring method is designed so that each item in the checklist is awarded zero or one point, with zero indicating lack of skill and one is indicating proficiency in the relevant area. Thus, participants' skills levels are determined and categorized.

02

Conditions studied

  • Chestcompressionadequacy

Keywords

  • CPR, metrics
03

In context

Lead sponsor

National Hepatology & Tropical Medicine Research Institute is the lead sponsor of 20 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Other
    CPR competency pre and post ALS Course

    assessment of participants prior to initiation of ALS course

    Other: Education (ALS provider course) in Egypt

Interventions

  • OtherEducation (ALS provider course) in Egypt

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

06

What researchers measure

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

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — results after acceptance for publication

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2025 (actual). Primary completion is estimated for Mar 2026, 9 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 22, 2025
First posted
Jul 25, 2025
StartActual
Jun 1, 2025
Primary completionEst.
Mar 1, 2026
CompletionEst.
Jun 1, 2026
Last update
Jul 25, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07085832
Lead sponsor
National Hepatology & Tropical Medicine Research Institute
Responsible party
ICU (Associate professor, National Hepatology & Tropical Medicine Research Institute) — Principal investigator
First posted
Jul 25, 2025
Start date
Jun 1, 2025
Primary completion
Mar 1, 2026 (estimated)
Completion
Jun 1, 2026 (estimated)
Last update
Jul 25, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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