- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03586752
CPR Education: Traditional Program Versus On-line Program
"iGOGO-Automated External Defibrillator Donation "Continuing Education Project
Out-of-hospital cardiac arrest (OHCA) is an important public health issue. Chang Gung Memorial Hospital, a university affiliated medical center in Taoyuan city, northern Taiwan, actively cooperated with the government policy to donate a total of 250 automated external defibrillators (AED) and to deploy them in public areas during the period of 2012 to 2014. In addition, nearly 200 courses of cardiopulmonary resuscitation (CPR) education for healthcare providers and citizens were provided.
In order to keep the skills and the abilities of emergency medical responses in these 200 and more AED recipient areas, repeated CPR education and training should be implemented. Quality assurance and regular follow-up by medical directors with professional advice and feedback can therefore be provided at the same time. Therefore, this project aims to assess the quality of emergency responses in the recipient units in the next four years via regular follow-up by medical directors with advice and feedback. Continuing medical education of both e-learning and classes, online registration system, as well as first aid supplies will be provided at the regular follow-up visits. The results of this project will provide a feasible model of quality assurance of first aid and AED implementation program in the community.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taoyuan, Taiwan, 333
- Chang Gung Memorial Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adults aged 20 and over
- Adults who have not attended CPR training for at least one year prior to enrollment
Exclusion Criteria:
- unable to kneel to practice CPR
- pregnant
- unwilling to sign informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: On-line group
On-line program course
|
18 minutes on-line video at home and 30 minutes CPR skill practice at scene in 3 days after watching on-line video
|
|
Active Comparator: Standard group
Standard program course
|
60-minute CPR teaching video with practice, 20 minutes of automated electrical defibrillator operation, and a 10-minute discussion with regard to the legal issues associated with bystander CPR in Taiwan
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Written test for knowledge about CPR
Time Frame: 4 days
|
Knowledge about CPR will be assessed via a written test before and after the CPR training.
The test includes 25 questions with a total score of 100 (4 points for each).
|
4 days
|
|
CPR flow checklist
Time Frame: 4 days
|
An evaluator who is blinded to the training allocation will assess the performance of CPR via a flow checklist.
A total of 20 items will be checked with a maximum sum score of 40 points.
|
4 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The percentage of correct depth of all compressions
Time Frame: 90 minutes
|
The percentage of correct depth (5-6 centimeters) of all compressions will be assessed by High Quality CPR (HQCPR). HQCPR is a machine with interactive response system which can provide information while performing CPR on manikin (Laerdal, Resusci Anne QCPR). |
90 minutes
|
|
The percentage of correct speed of compressions of all compressions
Time Frame: 90 minutes
|
The percentage of correct speed of compressions (100 to 200 per minute) of all compressions will be assessed by HQCPR. HQCPR is a machine with interactive response system which can provide information while performing CPR on manikin (Laerdal, Resusci Anne QCPR). |
90 minutes
|
|
The percentage of correct recoil of all compressions
Time Frame: 90 minutes
|
The percentage of correct recoil (full chest recoil) of all compressions will be assessed by HQCPR. HQCPR is a machine with interactive response system which can provide information while performing CPR on manikin (Laerdal, Resusci Anne QCPR). |
90 minutes
|
|
The average compression depth
Time Frame: 90 minutes
|
The average compression depth (unit in centimeter) is calculated by summing up the depth of each compression then to be divided by the number of total compressions. The compression depth is recorded by HQCPR. HQCPR is an interactive response machine to provide the information on depth, speed and recoil while performing CPR on manikin (Laerdal, Resusci Anne QCPR). |
90 minutes
|
|
The average compression speed
Time Frame: 90 minutes
|
The average compression speed is presented as the number of compressions per minute by HQCPR. HQCPR is an interactive response machine to provide the information on depth, speed and recoil while performing CPR on manikin (Laerdal, Resusci Anne QCPR). |
90 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Cheng-Yu Chien, Dr., Chang Gung Memorial Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- GMRPG3F1273
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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