Effect of AED-optimized Telephone-assisted CPR Instructions on No-flow Time and Chest Compression Fraction

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Minor Trial completed Show 4 more changesShow less
    • Final enrollment: 100 participants (planned 80)
    • Study completion date changed from estimate of Oct 30, 2026 to Sep 20, 2026
    • Eligibility criteria expanded, about 7 words
    • Publications: details revised at 1 of 1 entry
  2. Minor Enrollment closed, study ongoing
    • Primary completion pushed from Aug 31, 2026 to Sep 30, 2026
    • Study completion pushed from Sep 30, 2026 to Oct 30, 2026
    • Site details revised
    v4
  3. Minor Primary completion pushed from Jul 31, 2026 to Aug 31, 2026
    • Study completion pushed from Aug 31, 2026 to Sep 30, 2026
    • Start date changed from estimate of May 1, 2026 to Jul 10, 2026
    v3
  4. Minor Re-verified, no change to tracked fieldsv2
  5. Minor Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Out-of-hospital cardiac arrest (OHCA) remains a leading cause of mortality worldwide, with survival highly dependent on the immediate initiation of bystander cardiopulmonary resuscitation (CPR). Early recognition, prompt chest compressions, and rapid defibrillation are critical components of the chain of survival. Telephone-assisted CPR (T-CPR) provided by emergency dispatchers has been shown to significantly increase bystander intervention rates and improve outcomes. While the availability and use of automated external defibrillators (AEDs) further enhance survival, the optimal integration of AED use into dispatcher-guided, single-rescuer scenarios remains insufficiently studied. This prospective, randomized, controlled simulation study aims to evaluate the effect of modified telephone cardiopulmonary resuscitation (T-CPR) instructions optimized for automated external defibrillator (AED) use on no-flow time and chest compression fraction (CCF) during single-rescuer resuscitation. Participants are randomized to receive either standard T-CPR instructions or enhanced instructions focusing on minimizing interruptions in chest compressions and reducing time to first compression during AED use.
Trial Details
NCT Number NCT07520877
Lead Sponsor University of Pecs
Conditions
(from sponsor)
Cardiac Arrest (CA)
Related terms Heart Arrest
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov