The Effect of Attention Distractor on the Quality of Chest Compression

May 20, 2017 updated by: Joon Min Park, Inje University

The Effect of Attention Distractor During Cardiopulmonary Resuscitation on the Quality of Chest Compression: Randomized Crossover Trial With Simulated Situation

The investigators plan to investigate the effect of attention distractor on the quality of chest compression during cardiopulmonary resuscitation. For this, a simulated study with Manikin is performed and the paced auditory serial addition test (PASAT) is used for distracting performer's attention.

Study Overview

Study Type

Interventional

Enrollment (Actual)

44

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

      • Goyang-si, Korea, Republic of, 10380
        • Inje University Ilsan Paik Hospital

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 and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • healthy volunteers who completed basic life support course among medical personnel (doctors, nurses, paramedics) working in a university hospital

Exclusion Criteria:

  • pregnancy

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: HEALTH_SERVICES_RESEARCH
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
OTHER: CPR with attention distraction first
First, they perform two-minute chest compressions with conducting the PASAT. After 20 mins' rest, they perform two-minute chest compressions without conducting the PASAT.
A number between 1 to 9 is called every three seconds through a speaker, and the performer calculates the last two numbers and shouts the answer.
OTHER: CPR without attention distraction first
First, they perform two-minute chest compressions without conducting the PASAT. After 20 mins' rest, they perform two-minute chest compressions with conducting the PASAT.
A number between 1 to 9 is called every three seconds through a speaker, and the performer calculates the last two numbers and shouts the answer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
adequate compression rate
Time Frame: two minutes
the percentage of chest compression with adequate rate (100-120 per minute) during two-minute chest compression. Formula(%)=number of adequate chest compressions (rate:100-120/min) x 100 / number of all chest compressions during two minutes
two minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
adequate compression depth
Time Frame: two minutes
the percentage of chest compression with adequate depth (5-6cm) during two-minute chest compression. Formula(%)= number of adequate chest compressions(depth=5-6cm)x 100 / all chest compressions during two minutes
two minutes
adequate chest recoil
Time Frame: two minutes
the percentage of chest compression with adequate chest recoil during two-minute chest compression. Formula(%)=number of adequate chest recoils(automatically measured with simulator) x 100/ number of all chest compressions during two minutes
two minutes
mean compression rate
Time Frame: two minutes
Average of compression rate during two-minute chest compression. The scale for this outome is 'number per minute'.
two minutes
mean compression depth
Time Frame: two minutes
Average of compression depth during two-minute chest compression. The scale for this outcome is 'cm'.
two minutes
Subjective difficulty
Time Frame: Two minutes
Each performer rate the subjective difficulties of two arms with the 100mm VAS (0: very easy, 100: very difficult)
Two minutes

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Joon Min Park, Inje University Ilsan Paik Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (ACTUAL)

April 27, 2017

Primary Completion (ACTUAL)

May 14, 2017

Study Completion (ACTUAL)

May 20, 2017

Study Registration Dates

First Submitted

April 18, 2017

First Submitted That Met QC Criteria

April 18, 2017

First Posted (ACTUAL)

April 21, 2017

Study Record Updates

Last Update Posted (ACTUAL)

May 23, 2017

Last Update Submitted That Met QC Criteria

May 20, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 2017-04-007

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Cardiopulmonary Resuscitation, Simulation Training

Clinical Trials on paced auditory serial addition test (PASAT)

3
Subscribe