UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000059196 |
|---|---|
| Receipt number | R000067704 |
| Scientific Title | The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial. |
| Date of disclosure of the study information | 2025/09/26 |
| Last modified on | 2025/09/26 02:13:06 |
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Basic information
Public title
The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial.
Acronym
The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial.
Scientific Title
The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial.
Scientific Title:Acronym
The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial.
Region
| Japan |
Condition
Condition
none
Classification by specialty
| Emergency medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The objective is to determine whether fifth-year primary school pupils can perform appropriate chest compressions one year after receiving either CPR training emphasising the quality of chest compressions or training emphasising positive motivation.
Basic objectives2
Others
Basic objectives -Others
The objective is to determine whether fifth-year primary school pupils can perform appropriate chest compressions one year after receiving either CPR training emphasising the quality of chest compressions or training emphasising positive motivation.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Average depth of chest compressions (mm) performed during one minute one year after attending the training course.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -investigator(s) and assessor(s) are blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Other |
Interventions/Control_1
During the training session, perform cardiopulmonary resuscitation (CPR) training with the sound-producing surface facing upwards, utilising the 30kg force of Appa-kun. Throughout the training, use the same surface; do not change surfaces even if the sound does not produce effectively.
Interventions/Control_2
During the training session, perform CPR training with the sound-producing surface facing upwards, utilising the 10kg force of Appa-kun. Throughout the training, use the same surface; do not change surfaces even if the sound does not produce properly.
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
| 10 | years-old | <= |
Age-upper limit
| 11 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Primary schools whose headteachers have approved participation in this research for Year 5 pupils attending the Junior First Aid Course run by Toyonaka City Fire Department.
Key exclusion criteria
The purpose of this study is to verify differing educational effects; therefore, individuals who have previously received other training or for whom outcome measurement is difficult will be excluded. 1. Individuals unable to perform chest compressions and use an AED due to physical or mental reasons 2. Individuals for whom consent cannot be obtained from both the parent and the individual themselves 3. Individuals unable to participate in the full course of instruction and assessment 4. Individuals who have received training in cardiopulmonary resuscitation prior to this study 5. Other individuals deemed unsuitable by the researchers, considering the potential physical and mental impact on children
Target sample size
240
Research contact person
Name of lead principal investigator
| 1st name | Taku |
| Middle name | |
| Last name | Iwami |
Organization
Graduate School of Medicine and Faculty of Medicine, Kyoto University
Division name
Department of Preventive Services
Zip code
606-8501
Address
Yoshida Konoe chou, Sakyo-ku, Kyoto city
TEL
075-753-9301
kidscpr_rct@yobou.med.kyoto-u.ac.jp
Public contact
Name of contact person
| 1st name | Yusuke |
| Middle name | |
| Last name | Ito |
Organization
Graduate School of Medicine and Faculty of Medicine, Kyoto University
Division name
Department of Preventive Services
Zip code
606-8501
Address
Yoshida Konoe chou, Sakyo-ku, Kyoto city
TEL
075-753-9301
Homepage URL
kidscpr_rct@yobou.med.kyoto-u.ac.jp
Sponsor or person
Institute
Kyoto university
Institute
Department
Personal name
Funding Source
Organization
Operating Expenses - Education - Educational Research Project Expenses
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
Kyoto University Graduate School and Faculty of Medicine, Ethics Committee
Address
Yoshida Konoe chou, Sakyo-ku, Kyoto city
Tel
075-366-7618
ethcom@kuhp.kyoto-u.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
| 2025 | Year | 09 | Month | 26 | 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
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
Preinitiation
Date of protocol fixation
| 2025 | Year | 09 | Month | 25 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 10 | Month | 08 | Day |
Last follow-up date
| 2028 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 09 | Month | 26 | Day |
Last modified on
| 2025 | Year | 09 | Month | 26 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067704
