- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03124290
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
Status
Completed
Intervention / Treatment
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.
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