UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000059712 |
|---|---|
| Receipt number | R000067451 |
| Scientific Title | A Prospective Crossover Study on the Quality of Chest Compressions Performed on a Moving EMS Stretcher at Different Height Settings Using a CPR Training Simulator |
| Date of disclosure of the study information | 2025/11/10 |
| Last modified on | 2025/11/10 08:43:17 |
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Basic information
Public title
A Prospective Crossover Study on the Quality of Chest Compressions Performed on a Moving EMS Stretcher at Different Height Settings Using a CPR Training Simulator
Acronym
A Prospective Crossover Study on the Quality of Chest Compressions Performed on a Moving EMS Stretcher at Different Height Settings Using a CPR Training Simulator
Scientific Title
A Prospective Crossover Study on the Quality of Chest Compressions Performed on a Moving EMS Stretcher at Different Height Settings Using a CPR Training Simulator
Scientific Title:Acronym
A Prospective Crossover Study on the Quality of Chest Compressions Performed on a Moving EMS Stretcher at Different Height Settings Using a CPR Training Simulator
Region
| Japan |
Condition
Condition
cardiopulmonary arrest
Classification by specialty
| Emergency medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The objective of this study is to investigate the effect of different stretcher heights during transportation on the quality of chest compressions.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Laerdal CPR score
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -no one is blinded
Control
No treatment
Stratification
YES
Dynamic allocation
YES
Institution consideration
Institution is not considered as adjustment factor.
Blocking
YES
Concealment
Central registration
Intervention
No. of arms
6
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Maneuver |
Interventions/Control_1
Height ABC
Interventions/Control_2
Height ACB
Interventions/Control_3
Height BAC
Interventions/Control_4
Height BCA
Interventions/Control_5
Height CAB
Interventions/Control_6
Height CBA
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Physicians and nurses aged 20 years or older, engaged in emergency medical services.
Key exclusion criteria
Individuals with underlying conditions requiring exercise restriction, those who do not provide informed consent, or those who fail to achieve guideline-based CPR quality in the pre-test.
Target sample size
24
Research contact person
Name of lead principal investigator
| 1st name | Ryo |
| Middle name | |
| Last name | Ayata |
Organization
Yamaguchi University Hospital
Division name
Advanced Medical Emergency and Critical Care Center
Zip code
755-8505
Address
1-1-1, Minami-Kogushi, Ube, YAMAGUCHI, 755-8505, Japan.
TEL
0836222343
ryoayata@yamaguchi-u.ac.jp
Public contact
Name of contact person
| 1st name | Ryo |
| Middle name | |
| Last name | Ayata |
Organization
Yamaguchi University Hospital
Division name
Advanced Medical Emergency and Critical Care Center
Zip code
755-8505
Address
1-1-1, Minami-Kogushi, Ube, YAMAGUCHI, 755-8505, Japan.
TEL
0836222343
Homepage URL
ryoayata@yamaguchi-u.ac.jp
Sponsor or person
Institute
Yamaguchi University
Institute
Department
Personal name
Funding Source
Organization
Yamaguchi 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
Center for clinical research Yamaguchi university hospital
Address
1-1-1, Minami-Kogushi, Ube, YAMAGUCHI, 755-8505, Japan.
Tel
0836-22-2428
me223@yamaguchi-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 | 11 | Month | 10 | 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
Enrolling by invitation
Date of protocol fixation
| 2025 | Year | 08 | Month | 01 | Day |
Date of IRB
| 2025 | Year | 11 | Month | 04 | Day |
Anticipated trial start date
| 2025 | Year | 11 | Month | 10 | Day |
Last follow-up date
| 2025 | Year | 12 | 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 | 11 | Month | 10 | Day |
Last modified on
| 2025 | Year | 11 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000067451
