UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000058975 |
|---|---|
| Receipt number | R000067447 |
| Scientific Title | Evaluation of A Virtual Reality Application for Neonatal Resuscitation Training |
| Date of disclosure of the study information | 2025/09/03 |
| Last modified on | 2025/09/03 10:03:35 |
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Basic information
Public title
Evaluation of Neonatal Resuscitation Training VR
Acronym
Evaluate NCPR-VR
Scientific Title
Evaluation of A Virtual Reality Application for Neonatal Resuscitation Training
Scientific Title:Acronym
Evaluate NCPR-VR
Region
| Japan |
Condition
Condition
Healthy newborn healthcare providers
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
We developed a VR application that can contribute to the proficiency of neonatal resuscitation techniques among neonatal healthcare providers. The purpose of this study is to evaluate the developed VR application from the perspectives of usability and user experience.
Basic objectives2
Others
Basic objectives -Others
Usability, ease of use
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The score of System Usability Scale
Key secondary outcomes
SUS, IPQ, UEQ, SSQ scores. Participant feedback (free text), subjective evaluation of usefulness.
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Other |
Interventions/Control_1
Learning experiences using VR applications
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
1) Be a physician, nurse, or midwife engaged in perinatal care.
2) Hold a valid NCPR certification. The type of NCPR certification is not restricted.
Key exclusion criteria
1) Individuals prone to motion sickness or dizziness
2) Individuals deemed ineligible by the principal investigator or liaison officer
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Masato |
| Middle name | |
| Last name | Eto |
Organization
Graduate School of Medicine, The University of Tokyo
Division name
Department of Medical Education Studies, International Research Center for Medical Education
Zip code
113-0033
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan
TEL
03-5841-3303
amari-shoichiro158@g.ecc.u-tokyo.ac.jp
Public contact
Name of contact person
| 1st name | Shoichiro |
| Middle name | |
| Last name | Amari |
Organization
Graduate School of Medicine, The University of Tokyo
Division name
Reproductive, Developmental and Aging Sciences,
Zip code
113-0033
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan
TEL
090-1429-8589
Homepage URL
amari-shoichiro158@g.ecc.u-tokyo.ac.jp
Sponsor or person
Institute
The University of Tokyo
Institute
Department
Personal name
Funding Source
Organization
The University of Tokyo
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
Research Ethics Committee, Graduate School of Medicine, The University of Tokyo
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan
Tel
03-5841-3303
ethics@m.u-tokyo.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 | 03 | 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
Open public recruiting
Date of protocol fixation
| 2025 | Year | 09 | Month | 02 | Day |
Date of IRB
| 2025 | Year | 08 | Month | 07 | Day |
Anticipated trial start date
| 2025 | Year | 09 | Month | 03 | Day |
Last follow-up date
| 2026 | 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 | 03 | Day |
Last modified on
| 2025 | Year | 09 | Month | 03 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067447
