CPR Surface Choice on Chest Compression Quality

NCT ID: NCT06406101

Last Updated: 2024-10-08

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

147 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-08

Study Completion Date

2024-05-15

Brief Summary

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The objective of our randomized simulation study on mannequins with a population of Basic Life Support students is to compare the quality of chest compressions, taking depth as the main variable, in two simulated scenarios of out-of-hospital cardiac arrest on a bed: one where Cardiopulmonary Resuscitation is performed on the bed and another where the patient is transferred to the ground for Cardiopulmonary Resuscitation.

Detailed Description

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Conditions

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Cardiac Arrest Simulation of Physical Illness

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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Floor

Group Type EXPERIMENTAL

Floor

Intervention Type OTHER

Uninterrupted 2-minute chest compressions on a manikin that has been moved from the bed to the floor in a simulated scenario of out-of-hospital cardiac arrest

Bed

Group Type ACTIVE_COMPARATOR

Bed

Intervention Type OTHER

Uninterrupted 2-minute chest compressions on a manikin that is laying on bed in a simulated scenario of out-of-hospital cardiac arrest

Interventions

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Floor

Uninterrupted 2-minute chest compressions on a manikin that has been moved from the bed to the floor in a simulated scenario of out-of-hospital cardiac arrest

Intervention Type OTHER

Bed

Uninterrupted 2-minute chest compressions on a manikin that is laying on bed in a simulated scenario of out-of-hospital cardiac arrest

Intervention Type OTHER

Eligibility Criteria

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Exclusion Criteria

* Arthritis
* Heart disease
* Advanced lung disease
* Severe physical disability
* Morbid obesity
* Chronic fatigue
* Pregnancy

Withdrawal Criteria:

* Those individuals who, due to limitations in physical exercise, do not reach 2 minutes of compressions
* Students who have not obtained the certificate of successfully completing the course.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hospital Clinic of Barcelona

OTHER

Sponsor Role lead

Responsible Party

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Enrique Carrero

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Adriana Capdevila, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Clinic Barcelona, Universitat de Barcelona

Locations

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Hospital Clinic Barcelona

Barcelona, , Spain

Site Status

Countries

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Spain

Other Identifiers

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HCBCPR_24147

Identifier Type: -

Identifier Source: org_study_id

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