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Completed

NCT Number: NCT06794398

Feasibility of Appropriate Smartphone Position During Video-assisted Cardiopulmonary Resuscitation

There is a gap in our knowledge regarding whether video-assisted cardiopulmonary resuscitation (V-CPR) is feasible when a lay responder is alone at the scene. The feasibility of V-CPR was measured in a simulated cardiac arrest scenario when a lay responder was alone with the patient.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Human Patient Simulation Center

Pécs, 7621, Hungary

About this study

There is a gap in our knowledge regarding whether video-assisted cardiopulmonary resuscitation (V-CPR) is feasible when a lay responder is alone. The feasibility of V-CPR was measured in a simulated cardiac arrest scenario when a lay responder was alone with the patient. A pilot study was conducted to measure the appropriate smartphone position and placement time when a lay responder is alone. Two simulated cardiac arrest locations were prepared: a living room and yard.

The performance of the participants were recorded. After that, the quality and assessability of the videos were evaluated by five experts (experienced in CPR teaching and evaluation).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • layperson or health care professional, who is phisically and mentally able to do a simulated CPR scenario (participants in the scenario)
  • expert in CPR training (assessors)

Exclusion criteria

  • technical issue during data collection

Treatment and study plan

V-CPR inside a room when the lay responder is alone (no operator for holding the phone)

Device

Participants should find an appropriate smartphone position when they were able to use any objects in their environment. Participants get video-based (vocal and visual) instructions from the dispatcher during the V-CPR situation.

V-CPR in a yard (outside environment) when the lay responder is alone (no operator for holding the phone)

Device

Participants should find an appropriate smartphone position when they were able to use any objects in their environment. Participants get video-based (vocal and visual) instructions from the dispatcher during the V-CPR situation.

Primary outcomes

  1. Smartphone camera placement and perspective (used objects and visible environment)

    Time frame: During procedure

    Evaluating the used object (chair, table, shue, etc) to stabilize the smartphone for V-CPR in the prepared environment (a photo was taken by the study operator).

    Evaluating smartphone camera perspective by the dispatcher's laptop screen (smartphone camera picture was transferred via Microsoft Teams from the smartphone to the laptop during a live video-stream (to see what the dispatcher did see). Live video-stream was also recorded for post-analysis.

Secondary outcomes

  1. Smartphone camera placement time (time to the first chest compression)

    Time frame: During procedure

    Measuring the time from the dispatcher's instructions to the first chest compression (putting the hand on the patient's chest) based on the recorded video.

Other outcomes

  1. General quality of the video-records (clarity, lagging, camera perspective, visibility of chest compressions; by using a Likert-scale: from "1 - very bad quality" to "4 - very good quality")

    Time frame: During post-analysis of the video-records (within 1 week after data collection)

    Measuring the general quality of the video-records (Is chest compression depth, rate and hand position visible?; clarity and lagging of the video-record) based on the assessors subjective answers by using a Likert-scale: from "1 - very bad quality" to "4 - very good quality").

Sponsors and collaborators

Lead sponsor

University of Pecs

Other

Registry information

Official study title

Feasibility of Appropriate Smartphone Position During Video-assisted Cardiopulmonary Resuscitation When the Bystander is Alone At the Scene - a Randomized Controlled Crossover Simulation Trial

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jan 27, 2025
Registry last updated
Jan 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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