UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000054294 |
|---|---|
| Receipt number | R000062015 |
| Scientific Title | The Shift in Motivation for Disaster Preparedness among Health Nurses through VR-based Disaster Education |
| Date of disclosure of the study information | 2025/04/01 |
| Last modified on | 2025/05/01 09:48:29 |
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Basic information
Public title
The Shift in Motivation for Disaster Preparedness among Health Nurses through VR-based Disaster Education
Acronym
The Shift in Motivation for Disaster Preparedness among Health Nurses through VR-based Disaster Education
Scientific Title
The Shift in Motivation for Disaster Preparedness among Health Nurses through VR-based Disaster Education
Scientific Title:Acronym
The Shift in Motivation for Disaster Preparedness among Health Nurses through VR-based Disaster Education
Region
| Japan |
Condition
Condition
Public Health Nurses in Areas Designated for Special Strengthening of Tsunami Evacuation Measures in the Nankai Trough Earthquake Zone
Classification by specialty
| Nursing |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Conduct a quantitative study where data is collected through surveys or assessments measuring the perceived severity and likelihood of disaster scenarios among municipal public health nurses. Implement the intervention program with a controlled group, while another group serves as a comparison. Analyze the data collected before and after the intervention to determine any significant changes in threat assessment and response evaluation.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Design an experimental study where municipal public health nurses are randomly assigned to either a control group or an intervention group. The control group receives traditional training methods, while the intervention group undergoes VR-based training sessions focused on enhancing their self-efficacy, perception of severity, and likelihood of health crisis scenarios. Assessments are conducted before and after the intervention to measure any changes in the participants' perceptions. Statistical analysis is then performed to compare the outcomes between the two groups.
Key secondary outcomes
Conduct an experimental study where municipal public health nurses are randomly assigned to either a control group or an intervention group. The control group receives traditional training methods, while the intervention group undergoes VR-based training sessions focused on improving threat assessment and response evaluation skills. Assessments are conducted before and after the intervention to measure any changes in the participants' abilities to assess threats and evaluate responses. Statistical analysis is then performed to compare the outcomes between the two groups.
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
| Behavior,custom |
Interventions/Control_1
The researchers will conduct programs for participants that incorporate VR technology.
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
| 18 | years-old | < |
Age-upper limit
| 70 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Public health nurses in municipalities designated as special reinforcement areas for Nankai Trough earthquake and tsunami evacuation measures.
Key exclusion criteria
1.Individuals experiencing symptoms resembling PTSD based on past experiences.
2.Individuals with severe motion sickness.
3.Individuals unable to attend the intervention program sessions.
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Asami |
| Middle name | |
| Last name | Sasaki |
Organization
Graduate School of Medical Sciences, master's Program in Nursing, University of Fukui
Division name
Disaster nursing Certified Nurse Specialist
Zip code
910-1106
Address
Fukuiken yosidagun eiheijityou matuoka gokuryou 1003 hureriagakuentosi313
TEL
09051839915
sk23802@g.u-fukui.ac.jp
Public contact
Name of contact person
| 1st name | Asami |
| Middle name | |
| Last name | Sasai |
Organization
Graduate School of Medical Sciences master's Program in Nursing University of Fukui
Division name
Disaster nursing Certified Nurse Specialist
Zip code
910-1106
Address
Fukuiken yosidagun eiheijityou matuoka gokuryou 1003 hureriagakuentosi313
TEL
09051839915
Homepage URL
sk23802@g.u-fukui.ac.jp
Sponsor or person
Institute
University of Fukui
Institute
Department
Personal name
Funding Source
Organization
Japanese Red Cross Nursing Association
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Graduate School of Medical Sciences master's Program in Nursing University of Fukui
Address
Fukuiken Yosidagun Eiheijityou Matuoka Simoaiduki 23-3
Tel
0770613111
sk23802@g.u-fukui.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 | 04 | Month | 01 | 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
9
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 | 06 | Month | 30 | Day |
Date of IRB
| 2024 | Year | 08 | Month | 09 | Day |
Anticipated trial start date
| 2024 | Year | 06 | Month | 30 | Day |
Last follow-up date
| 2025 | 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
| 2024 | Year | 05 | Month | 01 | Day |
Last modified on
| 2025 | Year | 05 | Month | 01 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062015
