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Completed

NCT Number: NCT02073539

The Manikin Study of Chest Compression With One Accelerometer Feedback Device

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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Key information

Conditions

Cardiac Arrest Cardiovascular Diseases Heart Arrest Heart Diseases

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hanyang University Seoul Hospital

Seoul, 133792, South Korea

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Wrist or Low back disease

Treatment and study plan

Stryker ST104-747

Device

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

Other names: Transport stretcher®

Shinchang SB-34p

Device

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

Other names: Transport stretcher®

Primary outcomes

  1. Chest compression depth

    Time frame: Within 1day

    Primary out come is measured by Resusci Anne Modular System Skill Reporter manikin (9.89 kg, Laerdal Medical, Orpington, UK)

Secondary outcomes

  1. Chest compression rate

    Time frame: Within 1day

    Secondary out is measured by Resusci Anne Modular System Skill Reporter manikin (9.89 kg, Laerdal Medical, Orpington, UK).

Sponsors and collaborators

Lead sponsor

Hanyang University Seoul Hospital

Other

Registry information

Official study title

The Method of Proper Chest Compression Depth With Conventional and One Accelerometer Feedback Device During CPR in Hospital

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Feb 27, 2014
Registry last updated
Mar 21, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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