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Effectiveness of Video-assisted Cardiopulmonary Resuscitation

Primary Purpose

Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
Hungary
Study Type
Interventional
Intervention
Video-assisted CPR
Telephone-assisted CPR
Sponsored by
University of Pecs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrest

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: healthy volunteer 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 psychological disabilities

Sites / Locations

  • University of Pécs

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

No Intervention

Arm Label

T-CPR

V-CPR

Unassisted CPR

Arm Description

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

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

CPR without dispatcher instructions.

Outcomes

Primary Outcome Measures

Quality of chest compressions (depth of chest compressions).
Chest compression depth will be evaluated by a manikin connected to a CPR software.
Quality of chest compressions (rate of chest compressions).
Chest compression rate will be evaluated by a manikin connected to a CPR software.
Quality of chest compressions (hand position of chest compressions).
Hand position during chest compression will be evaluated by observation.

Secondary Outcome Measures

Time factors of CPR
Measuring the time of check breathing, time to recognize cardiac arrest, time to first chest compression, and cumulative time of no-flow time by the CPR software and observation.
Attitude of bystanders.
Subjective feelings after performing CPR based on a short survey using Likert-scale based queries (lower numbers indicate worse, higher score indicates better opinion).

Full Information

First Posted
November 14, 2022
Last Updated
January 23, 2023
Sponsor
University of Pecs
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1. Study Identification

Unique Protocol Identification Number
NCT05639868
Brief Title
Effectiveness of Video-assisted Cardiopulmonary Resuscitation
Official Title
Is Video-assisted Cardiopulmonary Resuscitation More Effective Than Telephone-assisted or Not-instructed Cardiopulmonary Resuscitation by Laypeople? - a Randomized Controlled Simulation Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
December 1, 2022 (Actual)
Primary Completion Date
January 20, 2023 (Actual)
Study Completion Date
January 23, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pecs

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Sudden cardiac arrest is a major public health problem worldwide and it is one of the leading causes of death in industrialized countries. Emergency Medical Services (EMS) dispatchers play an important role to recognize cardiac arrest and give help to the lay first responder via telephone CPR (T-CPR) which improves survival rates. The current technology allows the live video connection between the scene and the dispatcher which provides the opportunity for video-assisted CPR (V-CPR) via the bystander smartphone. Effectiveness of V-CPR has only been investigated to a limited extent. Comparing effectiveness of V-CPR (effectiveness of chest compression, time parameters eg. time to first chest compression) to T-CPR and non-instructed CPR can be useful to implement V-CPR technology.
Detailed Description
Sudden cardiac arrest is a major public health problem worldwide and it is one of the leading causes of death in industrialized countries. EMS dispatchers play an important role to recognize cardiac arrest and give help to the lay first responder via telephone CPR (T-CPR) which improves survival rates. The current technology allows the live video connection between the scene and the dispatcher which provides the opportunity for video-assisted CPR (V-CPR) via the bystander smartphone. Effectiveness of V-CPR has only been investigated to a limited extent. Comparing effectiveness of V-CPR (quality of chest compressions: depth, rate, hand position), time parameters: time to recognize cardiac arrest, time of check breathing, total no-flow time, to first chest compression) to T-CPR and non-instructed CPR can be useful to implement V-CPR technology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
T-CPR
Arm Type
Active Comparator
Arm Description
Participants perform telephone-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Arm Title
V-CPR
Arm Type
Experimental
Arm Description
Participants perform video-assisted CPR based on the European Resuscitation Council (ERC) 2021 guidelines.
Arm Title
Unassisted CPR
Arm Type
No Intervention
Arm Description
CPR without dispatcher instructions.
Intervention Type
Other
Intervention Name(s)
Video-assisted CPR
Intervention Description
Participants in V-CPR group get video-based (vocal and visual) instructions from the dispatcher.
Intervention Type
Other
Intervention Name(s)
Telephone-assisted CPR
Intervention Description
Participants in T-CPR group get voice-based (vocal) instructions from the dispatcher.
Primary Outcome Measure Information:
Title
Quality of chest compressions (depth of chest compressions).
Description
Chest compression depth will be evaluated by a manikin connected to a CPR software.
Time Frame
During procedure
Title
Quality of chest compressions (rate of chest compressions).
Description
Chest compression rate will be evaluated by a manikin connected to a CPR software.
Time Frame
During procedure
Title
Quality of chest compressions (hand position of chest compressions).
Description
Hand position during chest compression will be evaluated by observation.
Time Frame
During procedure
Secondary Outcome Measure Information:
Title
Time factors of CPR
Description
Measuring the time of check breathing, time to recognize cardiac arrest, time to first chest compression, and cumulative time of no-flow time by the CPR software and observation.
Time Frame
During procedure
Title
Attitude of bystanders.
Description
Subjective feelings after performing CPR based on a short survey using Likert-scale based queries (lower numbers indicate worse, higher score indicates better opinion).
Time Frame
Immediately after the CPR procedure (within 15 minutes)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy volunteer 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 psychological disabilities
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bálint Bánfai, PhD
Organizational Affiliation
University of Pecs
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pécs
City
Pécs
ZIP/Postal Code
7621
Country
Hungary

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effectiveness of Video-assisted Cardiopulmonary Resuscitation

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