UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000061185 |
|---|---|
| Receipt number | R000064917 |
| Scientific Title | Changes in Awareness and Practices of Chest Compressions Among Elementary School Educators: Implementation of an Audio-Visual Feedback Device |
| Date of disclosure of the study information | 2026/04/30 |
| Last modified on | 2026/04/07 14:42:58 |
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Basic information
Public title
Changes in Awareness and Practices of Chest Compressions Among Elementary School Educators
Acronym
Changes in Awareness and Practices of Chest Compressions Among Elementary School Educators
Scientific Title
Changes in Awareness and Practices of Chest Compressions Among Elementary School Educators: Implementation of an Audio-Visual Feedback Device
Scientific Title:Acronym
Changes in Awareness and Practices of Chest Compressions Among Elementary School Educators: Implementation of an Audio-Visual Feedback Device
Region
| Japan |
Condition
Condition
None
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study is a comparative investigation targeting elementary school educators to evaluate the effectiveness of a training program implementation of an AVF device. It aims to elucidate changes in the participants' awareness and practices related to chest compressions before and after the program's implementation.
Basic objectives2
Others
Basic objectives -Others
1)Awareness of Chest Compressions (Knowledge): The number of correct answers in a written test on chest compressions conducted before and after the intervention.
2)Awareness of Chest Compressions (CPR Willingness): The results of the willingness to perform CPR, evaluated before and after the intervention.
3)Quality of Chest Compressions: Measured using a skill report during a school-age model, including:
Compression depth (mm)
Compression rate (compressions per minute)
Percentage of recoil (the rate at which the chest wall returns to the position before compression is released).
Trial characteristics_1
Others
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
1)Awareness of Chest Compressions (Knowledge): The number of correct answers in a written test on chest compressions conducted before and after the intervention.
2)Awareness of Chest Compressions (CPR Willingness): The results of the willingness to perform CPR, evaluated before and after the intervention.
3)Quality of Chest Compressions: Measured using a skill report during a school-age model, including:
Compression depth (mm)
Compression rate (compressions per minute)
Percentage of recoil (the rate at which the chest wall returns to the position before compression is released).
Key secondary outcomes
1)Age
2)Gender
3)Height
4)Weight
5)Years of teaching experience
6)Experience in CPR training
7)Number of years since last CPR training Experience with training using schoolchildren models
8)Experience in resuscitation and lifesaving procedures
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
NO
Dynamic allocation
NO
Institution consideration
Institution is not considered as adjustment factor.
Blocking
NO
Concealment
No need to know
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Maneuver |
Interventions/Control_1
This is a CPR training session for school staff, consisting of practical instruction using a child mannequin with audiovisual feedback devices, as well as a lecture.
The entire intervention lasts approximately 50 minutes per session.
During the first practical session, participants perform 90 consecutive chest compressions on a pediatric manikin using an audiovisual feedback device.
Participants perform the procedure one at a time. Based on an objective evaluation using a skill reporter, the instructor provides approximately 2 minutes of individual verbal feedback regarding compression location, posture, and technique. While waiting, participants engage in self-study by watching case videos and reviewing materials on AED usage. This session lasts approximately 15 minutes.
General Lecture
The instructor delivers a lecture on basic life support. Duration: approximately 5 minutes.
For the second practical session, participants perform 90 chest compressions on a pediatric manikin using an audiovisual feedback device, similar to the first session.
Participants perform the procedure while monitoring the quality of their chest compressions in real time via the app screen. To minimize the effects of fatigue, the session is conducted in the same order as the first, and the waiting time is used for self-study.
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
All staff working at the school
Key exclusion criteria
Conditions such as a wrist fracture that are expected to interfere with performing chest compressions.
School nurses are excluded from this requirement, as they are expected to be licensed nurses or public health nurses.
Individuals who have obtained a license in basic life support or hold a medical license.
Target sample size
60
Research contact person
Name of lead principal investigator
| 1st name | kaede |
| Middle name | |
| Last name | Mizushima |
Organization
Tokyo Healthcare University
Division name
Higashigaoka faculty of nursing
Zip code
1520021
Address
2-5-1,Meguro-ku,Tokyo
TEL
03-5779-5031
kg024024@thcu.ac.jp
Public contact
Name of contact person
| 1st name | Kaede |
| Middle name | |
| Last name | Mizushima |
Organization
Tokyo Healthcare University
Division name
Tokyo Healthcare University
Zip code
1520021
Address
2-5-1, Meguro-ku, Tokyo
TEL
03-5779-5032
Homepage URL
kg024024@thcu.ac.jp
Sponsor or person
Institute
Tokyo Healthcare University
Institute
Department
Personal name
Funding Source
Organization
Tokyo Healthcare University
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Tokyo University of Health Science Ethics Commitee on Human Research
Address
4-1-17 Higashi-Gotanda, Shinagawa-ku, Tokyo
Tel
03-5721-7655
rinri@thcu.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 04 | Month | 30 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
31
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2024 | Year | 10 | Month | 22 | Day |
Date of IRB
| 2024 | Year | 12 | Month | 20 | Day |
Anticipated trial start date
| 2025 | Year | 02 | Month | 17 | Day |
Last follow-up date
| 2025 | Year | 04 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2026 | Year | 04 | Month | 07 | Day |
Last modified on
| 2026 | Year | 04 | Month | 07 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064917
