Effectiveness of Video-assisted Cardiopulmonary Resuscitation

NCT ID: NCT05639868

Last Updated: 2023-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2023-01-23

Brief Summary

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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

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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.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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T-CPR

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

Group Type ACTIVE_COMPARATOR

Video-assisted CPR

Intervention Type OTHER

Participants in V-CPR group get video-based (vocal and visual) instructions from the dispatcher.

Telephone-assisted CPR

Intervention Type OTHER

Participants in T-CPR group get voice-based (vocal) instructions from the dispatcher.

V-CPR

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

Group Type EXPERIMENTAL

Video-assisted CPR

Intervention Type OTHER

Participants in V-CPR group get video-based (vocal and visual) instructions from the dispatcher.

Telephone-assisted CPR

Intervention Type OTHER

Participants in T-CPR group get voice-based (vocal) instructions from the dispatcher.

Unassisted CPR

CPR without dispatcher instructions.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Video-assisted CPR

Participants in V-CPR group get video-based (vocal and visual) instructions from the dispatcher.

Intervention Type OTHER

Telephone-assisted CPR

Participants in T-CPR group get voice-based (vocal) instructions from the dispatcher.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Pecs

OTHER

Sponsor Role lead

Responsible Party

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Dr. Bálint Bánfai

senior lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Bálint Bánfai, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pecs

Locations

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University of Pécs

Pécs, , Hungary

Site Status

Countries

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Hungary

References

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Szollosi V, Horvath B, Nemeth D, Banfai-Csonka H, Betlehem J, Banfai B. A randomized controlled simulation trial comparing video-assisted with telephone-assisted and unassisted cardiopulmonary resuscitation performed by non-healthcare university students. Sci Rep. 2023 Sep 11;13(1):14925. doi: 10.1038/s41598-023-42131-z.

Reference Type DERIVED
PMID: 37696968 (View on PubMed)

Other Identifiers

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Upecs_V-CPR

Identifier Type: -

Identifier Source: org_study_id

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