Tilt Cardiopulmonary Resuscitation With a Feedback Device

August 25, 2014 updated by: Jaehoon Oh, Hanyang University
According to the European Resuscitation Council (ERC) Guidelines for patient to a depth of approximately 5-6 cm on a firm and flat surface when possible. However, Cardiopulmonary resuscitation (CPR) performers may need to continue the chest Resuscitation 2010, CPR performers should compress the sternum of a compression in an oblique direction, such as in elevators. For a pregnant patient in cardiac arrest, the 2010 ERC Guidelines recommend that the performer place the patient in a left-lateral tilt of 15 - 30° using a firm wedge to support the pelvis and thorax because the pregnant uterus can compress the inferior vena cava. We hypothesized Smartphone based chest compression feedback app would improves quality of CPR in an angulated surface.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
      • Seoul, Korea, Republic of, 133792
        • Hanyang University, College of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy person
  • > 18 years old
  • Basic life support educated person

Exclusion Criteria:

  • Cardiovascular disease
  • Musculoskeletal disease
  • Psychiatric disease
  • Pregnant
  • > 65 years old

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Without feedback
Participants compress the chest of the manikin without smartphone based feedback app.
Experimental: With feedback
Participants compress the chest of the manikin with a smartphone based feedback app.
Device: Audiovisual feedback from smartphone based app

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Chest compression depth
Time Frame: within the first 30 days after the end of recording
To measure chest compression depth during 2 minutes
within the first 30 days after the end of recording
Chest compression rate
Time Frame: within the first 30 days after the end of recording
To measure the chest compression rate during 2 minutes
within the first 30 days after the end of recording

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accurate chest compression
Time Frame: within the first 30 days after the end of recording
To measure the percentage of accurate chest compressions (i.e. correct depth, hand position, and recoil) of total chest compressions during 2 minutes
within the first 30 days after the end of recording

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Hanyang University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2014

Primary Completion (Actual)

August 1, 2014

Study Completion (Actual)

August 1, 2014

Study Registration Dates

First Submitted

June 25, 2014

First Submitted That Met QC Criteria

June 25, 2014

First Posted (Estimate)

June 26, 2014

Study Record Updates

Last Update Posted (Estimate)

August 27, 2014

Last Update Submitted That Met QC Criteria

August 25, 2014

Last Verified

August 1, 2014

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Tilt CPR

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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