Study of Telephone-assisted CPR Instructions Optimized for AED Use to Improve Chest Compressions and Reduce No-flow Time in Single-Rescuer Cardiac Arrest
Led by University of Pecs · Updated on 2026-07-13
80
Participants Needed
1
Research Sites
4 weeks
Total Duration
AI-Summary
What this Trial Is About
Out-of-hospital cardiac arrest OHCA is a leading cause of death worldwide, with survival depending heavily on immediate bystander cardiopulmonary resuscitation CPR. Early recognition, quick chest compressions, and rapid defibrillation are vital for increasing survival chances. This study evaluates how telephone-assisted CPR T-CPR instructions optimized for automated external defibrillator AED use affect no-flow time and chest compression fraction CCF during single-rescuer resuscitation.
Participants are randomly assigned to receive either standard T-CPR instructions or enhanced AED-optimized T-CPR instructions. The enhanced instructions focus on minimizing interruptions in chest compressions, reducing the time to the first compression, and improving AED use workflow. Key changes include immediate AED activation, starting compressions during AED voice prompts, continuing compressions during AED preparation and charging, and minimizing pauses before and after shock delivery.
Participants perform dispatcher-assisted CPR following European Resuscitation Council guidelines and the respective national protocols. Researchers measure no-flow time, time to first chest compression, time to first shock, chest compression fraction, and peri-shock pause during the procedure. The study is conducted as a prospective, randomized, controlled simulation, with participation lasting during the resuscitation simulation and data collection periods.
CONDITIONS
Brief Title
Effect of AED-optimized Telephone-assisted CPR Instructions on No-flow Time and Chest Compression Fraction
Research Team
B
Bálint Bánfai, Ph.D.
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People with cardio-pulmonary or musculoskeletal diseases or any condition that risks harm during CPR
Physical or psychological disabilities
Technical issues during data collection
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Simulation and Intervention
Duration - Single session during the study period
Participants perform dispatcher-assisted CPR following assigned instructions, either standard or AED-optimized, during a simulated single-rescuer cardiac arrest scenario.
1 session (in-person)
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
Dispatcher-assisted AED use in single-rescuer cardiac arrest: study protocol for a randomized simulation study comparing standard and optimized dispatcher-assisted CPR instructions.
Barnabás Balassa, Henrietta Bánfai-Csonka, József Betlehem...