- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02964832
Assessment of Chest Compression Depth Obtained Using the Smartphone Application as an Educational Tool With New Attachment Device
November 12, 2016 updated by: Joonbum Park, Soonchunhyang University Hospital
To improve the quality of CPR education, we want to assess the validity and reliability of the feedback depth measured by smartphone applications according to the smartphone attachment sites as an educational tool.
However, in the prior study, armband method showed overestimated chest compression depth.
The reason of the overestimation was analyzed that the weight of the smartphone amplified the inertial force to produce additional linear movement.
In this study, we will make new device to fix the smartphone on the arm and on the hand and compare the chest compression depth between CPR manikin and smartphone application.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
50
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 Contact
- Name: Joonbum Park, MD, PhD
- Phone Number: 82-2-709-9117
- Email: jesumania@gmail.com
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:
- BLS provider or instructor
Exclusion Criteria:
- one who has physical problem in chest compression
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: Diagnostic
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: PocketCPR;Grasp method
Subject grasp a smartphone in the hand and compress the chest of manikin.
|
|
Active Comparator: PocketCPR;Armband-in-hand method
Grab the smartphone-contained-armband in hand when performing chest compression
|
|
Active Comparator: PocketCPR;Armband-on-arm method
Fix the smartphone-contained-armband on upperarm when performing chest compression
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Assessment of validity of Chest compression depth by smartphone application,PocketCPR
Time Frame: Through study completion, average 4 weeks
|
Through study completion, average 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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
January 1, 2017
Primary Completion (Anticipated)
March 1, 2017
Study Completion (Anticipated)
June 1, 2017
Study Registration Dates
First Submitted
November 2, 2016
First Submitted That Met QC Criteria
November 12, 2016
First Posted (Estimate)
November 16, 2016
Study Record Updates
Last Update Posted (Estimate)
November 16, 2016
Last Update Submitted That Met QC Criteria
November 12, 2016
Last Verified
November 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- JPark1601
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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