V-CPR Under Special Circumstances

NCT ID: NCT07101510

Last Updated: 2025-09-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 157 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-10
• Study Completion Date: 2025-09-10

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.

Conditions

Cardiac Arrest (CA)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

sV-CPR

Participants perform video-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.

Group Type: EXPERIMENTAL

sV-CPR

Intervention Type: BEHAVIORAL

In the sV-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a video connection with a dispatcher located in another room using a smartphone. To simulate challenging conditions, they must carry out the task in near-total darkness, with the phone's flashlight as the only light source.

V-CPR

Participants perform video-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.

Group Type: ACTIVE_COMPARATOR

V-CPR

Intervention Type: BEHAVIORAL

In the V-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a video connection with a dispatcher located in another room using a smartphone.

T-CPR

Participants perform telephone-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.

Group Type: ACTIVE_COMPARATOR

T-CPR

Intervention Type: BEHAVIORAL

In the T-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a telephone connection with a dispatcher located in another room using a smartphone (vocal communication only).

sT-CPR

Participants perform telephone-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.

Group Type: EXPERIMENTAL

sT-CPR

Intervention Type: BEHAVIORAL

In the sT-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a telephone connection with a dispatcher located in another room using a smartphone (vocal communication only). To simulate challenging conditions, they must carry out the task in higher environmental noises (traffic), generated by a loudspeaker.

Interventions

sV-CPR

In the sV-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a video connection with a dispatcher located in another room using a smartphone. To simulate challenging conditions, they must carry out the task in near-total darkness, with the phone's flashlight as the only light source.

Intervention Type: BEHAVIORAL

V-CPR

In the V-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a video connection with a dispatcher located in another room using a smartphone.

Intervention Type: BEHAVIORAL

T-CPR

In the T-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a telephone connection with a dispatcher located in another room using a smartphone (vocal communication only).

Intervention Type: BEHAVIORAL

sT-CPR

In the sT-CPR group, participants manage a simulated cardiac arrest scenario alone. They perform CPR while establishing a telephone connection with a dispatcher located in another room using a smartphone (vocal communication only). To simulate challenging conditions, they must carry out the task in higher environmental noises (traffic), generated by a loudspeaker.

Intervention Type: BEHAVIORAL

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Pecs

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University of Pécs

Pécs, , Hungary

Countries

Hungary

Other Identifiers

V-CPR special circumstances

Identifier Type: -

Identifier Source: org_study_id