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The Manikin Study of Chest Compression With One Accelerometer Feedback Device

NCT ID: NCT02073539

Last Updated: 2014-03-21

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

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-03-31

Study Completion Date

2014-03-31

Brief Summary

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Chest compression (CC) feedback devices are used to perform CC measurements effectively and accurately on patients in hospital beds. However, these devices do not take account of the compression of the mattress, which results in overestimation of CC depth. This study is the validation study to demonstrate that a new method using one accelerometer(U-cpr) is useful to overcome this limitation and thus measure compression depth more accurately when performing cardiopulmonary resuscitation (CPR) on patients.

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Detailed Description

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Data collection The participants will be divided into three groups by random drawings. Each performer in the three-groups will compress the chest of the manikin on the bed with real-time 5cm,6cm and 7cm feed-back by one accelerometer (U-cpr).We will use two beds \[Stryker ST104-747(Transport stretcher®, 760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US) ,Shinchang SB-34p (Transport stretcher® , 850 x 2080 mm,Shinchang Co.,Busan,ROK)\]. Each participants will do 6 cycles of chest compression and 1cyle will be 2minutes. Between each cycles, participants will take a rest 5minutes.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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chest compression with 5cm feedback

We will feedback by one accelerometer (U-cpr). U-cpr is android based smartphone application.

Group Type EXPERIMENTAL

Stryker ST104-747

Intervention Type DEVICE

760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US

Shinchang SB-34p

Intervention Type DEVICE

, 850 x 2080 mm,Shinchang Co.,Busan,ROK

chest compression with 6cm feedback

We will feedback by one accelerometer(U-cpr). U-cpr is android based smartphone application.

Group Type EXPERIMENTAL

Stryker ST104-747

Intervention Type DEVICE

760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US

Shinchang SB-34p

Intervention Type DEVICE

, 850 x 2080 mm,Shinchang Co.,Busan,ROK

chest compression with 7cm feedback

We will feedback by one accelerometer(U-cpr). U-cpr is android based smartphone application.

Group Type EXPERIMENTAL

Stryker ST104-747

Intervention Type DEVICE

760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US

Shinchang SB-34p

Intervention Type DEVICE

, 850 x 2080 mm,Shinchang Co.,Busan,ROK

Interventions

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Stryker ST104-747

760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US

Intervention Type DEVICE

Shinchang SB-34p

, 850 x 2080 mm,Shinchang Co.,Busan,ROK

Intervention Type DEVICE

Other Intervention Names

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Transport stretcher® Transport stretcher®

Eligibility Criteria

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Inclusion Criteria

* Postgraduates year 1,2,3,4 and Emergency physicians in emergency department

Exclusion Criteria

* Wrist or Low back disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hanyang University Seoul Hospital

OTHER

Sponsor Role lead

Responsible Party

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Lee Sang Hyun

Clinical fellow

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sang hyun Lee, M.D

Role: PRINCIPAL_INVESTIGATOR

Hanyang University Seoul Hospital

Locations

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Hanyang University Seoul Hospital

Seoul, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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2013-12-010-001

Identifier Type: -

Identifier Source: org_study_id

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