Tokyo, Sept. 26 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059196) titled 'The effectiveness of educational method that emphasize the quality of chest compression in elementary schoolchildren: a single blind randomized control trial' on Sept. 26.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Single blind -investigator(s) and assessor(s) are blinded
Control - Active
Primary Sponsor:
Institute - Kyoto university
Condition:
Condition - none
Classification by malignancy - Others
Genomic information - NO
Objective:
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
Intervention:
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.
Eligibility:
Age-lower limit - 10
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 Size - 240
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 09 Month 25 Day
Anticipated trial start date - 2025 Year 10 Month 08 Day
Last follow-up date - 2028 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067704
Disclaimer: Curated by HT Syndication.
