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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05639868
Other study ID # Upecs_V-CPR
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date January 23, 2023

Study information

Verified date January 2023
Source University of Pecs
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date January 23, 2023
Est. primary completion date January 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Video-assisted CPR
Participants in V-CPR group get video-based (vocal and visual) instructions from the dispatcher.
Telephone-assisted CPR
Participants in T-CPR group get voice-based (vocal) instructions from the dispatcher.

Locations

Country Name City State
Hungary University of Pécs Pécs

Sponsors (1)

Lead Sponsor Collaborator
University of Pecs

Country where clinical trial is conducted

Hungary, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of chest compressions (depth of chest compressions). Chest compression depth will be evaluated by a manikin connected to a CPR software. During procedure
Primary Quality of chest compressions (rate of chest compressions). Chest compression rate will be evaluated by a manikin connected to a CPR software. During procedure
Primary Quality of chest compressions (hand position of chest compressions). Hand position during chest compression will be evaluated by observation. During procedure
Secondary 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. During procedure
Secondary 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). Immediately after the CPR procedure (within 15 minutes)
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