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MultiCPR: The Influence of Firefighter's PPE on Chest Compressions (MultiCPR3)

MultiCPR: The Influence of Firefighter's PPE on Chest Compressions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06986200
Acronym
MultiCPR3
Enrollment
38
Registered
2025-05-22
Start date
2025-06-16
Completion date
2025-12-01
Last updated
2026-01-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest (CA), Occupational Health

Brief summary

The aim of this clinical study is to evaluate the impact of wearing firefighters' personal protective equipment (PPE) on the quality of chest compressions during simulated resuscitation scenarios. The study compares the effects of one-minute versus two-minute intervals for switching the individual performing compressions. How does the clinical trial work? This randomized cross over trial will be conducted in several locations and will involve a total of 38 fire-fighters. The study will be conducted by the Department of Anesthesiology of the Medical University of Vienna. Participation in this clinical study is expected to last 30 minutes in total. Participants are randomized to either one or two minute intervalls of performing chest compressions in teams of two. After a cooling-of phase of at least 24 hours, they will be switched to the other group. Chest compressions will be performed for 12 minutes in full firefighter's PPE. Primary outcome will be chest compression depth.

Interventions

Performing chest compressions in full firefighter's personal protcetion equipment

PROCEDUREOne minute rotation intervall

Chest compressions using a one minute rotation intervall

PROCEDURETwo minute rotation intervall

Chest compressions using a two minute rotation intervall

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Inclusion: * Healthy fire-fighters trained in CPR * CPR Training in the last four years * Fit and rested Exclusion: \- Pregnant participants

Design outcomes

Primary

MeasureTime frameDescription
Chest Compressions depthduring 12 minutes of chest compressions. 2x12 = 24minutes in total per participantdepth in milimeter

Secondary

MeasureTime frameDescription
Chest compression rateduring 12 minutes of chest compressions. 2x12 = 24minutes in total per participant
Incomplete recoil (leaning) during chest compressionsduring 12 minutes of chest compressions. 2x12 = 24minutes in total per participantIncomplete recoil is an important measure during chest compressions as it impairs ventricular filling. Incomplete recoil is measured in milimeters.

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026