The Manikin Study of Chest Compression With One Accelerometer Feedback Device

Cardiac Arrest Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02073539
• Other study ID #: 2013-12-010-001
• Status: Completed
• Phase: N/A
• First received: February 24, 2014
• Last updated: March 20, 2014
• Start date: March 2014
• Est. completion date: March 2014

Study information

• Verified date: March 2014
• Source: Hanyang University Seoul Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Korea: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 19
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

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

Exclusion Criteria:

• Wrist or Low back disease

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Cardiac Arrest
• Heart Arrest

Intervention

Device:
• Stryker ST104-747
760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US
• Shinchang SB-34p
, 850 x 2080 mm,Shinchang Co.,Busan,ROK

Locations

Country	Name	City	State
Korea, Republic of	Hanyang University Seoul Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Hanyang University Seoul Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Chest compression depth	Primary out come is measured by Resusci Anne Modular System Skill Reporter manikin (9.89 kg, Laerdal Medical, Orpington, UK)	Within 1day	No
Secondary	Chest compression rate	Secondary out is measured by Resusci Anne Modular System Skill Reporter manikin (9.89 kg, Laerdal Medical, Orpington, UK).	Within 1day	No