Effectiveness of Video-assisted Cardiopulmonary Resuscitation Under Special Circumstances: a Randomized Controlled Simulation Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Pecs
- Enrollment
- 157
- Locations
- 1
- Primary Endpoint
- Chest compression depth
Study Overview
Brief Summary
Out-of-hospital cardiac arrest (OHCA) remains a major cause of death globally, with bystander CPR rates varying widely (13-82%) despite public health efforts. Early recognition, EMS activation, and immediate CPR are key to survival, often beginning with a layperson guided by an emergency dispatcher.
Telephone-assisted CPR (T-CPR), where dispatchers give verbal instructions, is common but limited-dispatchers can't see the scene or correct CPR technique. In contrast, video-assisted CPR (V-CPR) enables visual feedback, potentially improving performance in areas like compression rate and hand placement. However, evidence is mixed regarding its effect on compression depth, and initiating a video call may introduce delays.
While V-CPR's technical benefits have been studied, little is known about how real-world distractions-like noise or poor lighting-affect its effectiveness. Our simulation study aimed to compare T-CPR and V-CPR under both ideal and challenging conditions to assess the impact of environmental factors on layperson CPR quality and dispatcher support.
Detailed Description
Out-of-hospital cardiac arrest (OHCA) remains a major global health concern and one of the leading causes of mortality in industrialized nations. Despite various public health initiatives aimed at increasing layperson engagement in early intervention, bystander cardiopulmonary resuscitation (CPR) rates continue to vary widely across countries, ranging from 13% to 82%. Survival after OHCA is strongly associated with the early recognition of cardiac arrest, rapid activation of emergency medical services (EMS), and immediate initiation of effective CPR. In most cases, the first responder is a layperson who contacts the emergency dispatcher-making dispatcher-assisted CPR a critical link in the chain of survival.
Telephone-assisted CPR (T-CPR), where the dispatcher provides audio instructions, is a widely adopted and effective method to initiate life-saving efforts. However, the lack of visual feedback limits its potential: the dispatcher cannot observe the victim's condition, the responder's technique, or the scene dynamics. As a result, certain errors may go uncorrected, and the quality of CPR may be suboptimal.
With advancements in communication technology, real-time video communication between dispatchers and callers has become feasible. Video-assisted CPR (V-CPR) allows dispatchers to visually assess the situation, provide tailored feedback, and correct lay responder errors during the intervention. Several simulation studies have demonstrated that V-CPR can improve CPR performance compared to T-CPR, particularly in terms of compression rate, hand placement, and technique. However, the evidence regarding its superiority in achieving guideline-recommended compression depth remains mixed. Furthermore, the added complexity of initiating a video call and ensuring optimal camera positioning can delay CPR initiation and affect its effectiveness.
While prior studies have explored the technical feasibility and clinical benefits of V-CPR, the influence of environmental and situational variables-such as background noise, poor lighting conditions, or the presence of distractions-remains underexplored. These factors are highly relevant in real-world emergencies and may impact both the lay responder's performance and the dispatcher's ability to guide the process effectively.
Our study aimed to address this gap by conducting a simulation trial to compare the effectiveness of T-CPR and V-CPR under both ideal and environmentally challenging conditions. By systematically examining the impact of common distracting factors, our goal was to better understand the limitations and potential of video-assisted emergency guidance in realistic layperson resuscitation scenarios.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Investigator, Outcomes Assessor)
Masking Description
Participants will be informed about their group assignment post-randomization but will be blinded to the study's aims. The dispatcher and the simulation operator will be briefed on their specific tasks but will remain blinded to the study hypotheses and outcomes.
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •healthy voluntear
Exclusion Criteria
- •healthcare professionals (paramedics, nurses, etc.)
- •pregnant women
- •people with cardio-pulmonary and musculoskeletal diseases or any other impairment that would risk harm for the volunteer while performing CPR for 2 minutes
- •physical and/or psychological disabilities
- •technical issue during data collection
Arms & Interventions
sV-CPR
Participants perform video-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Intervention: sV-CPR (Behavioral)
V-CPR
Participants perform video-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Intervention: V-CPR (Behavioral)
T-CPR
Participants perform telephone-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Intervention: T-CPR (Behavioral)
sT-CPR
Participants perform telephone-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Intervention: sT-CPR (Behavioral)
Outcomes
Primary Outcomes
Chest compression depth
Time Frame: During procedure.
Chest compression depth will be evaluated by a manikin connected to a CPR software.
Secondary Outcomes
- Chest compression rate(During procedure)
- Hand position during chest compression.(During procedure)
