UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043209
Receipt number R000049316
Scientific Title Research on effective evacuation against tsunami using virtual reality
Date of disclosure of the study information 2021/02/01
Last modified on 2023/08/08 09:23:59

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Basic information

Public title

Research on effective evacuation against tsunami using virtual reality

Acronym

Research on tsunami evacuation using VR

Scientific Title

Research on effective evacuation against tsunami using virtual reality

Scientific Title:Acronym

Research on tsunami evacuation using VR

Region

Japan


Condition

Condition

Asymptomatic adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

In order to further enhance the reality of evacuation simulation, we will develop a tsunami simulation that combines VR and a walking controller, record evacuation behavior of participants, evaluate physiological and psychological states, and examine factors that influence these.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Heart rate, salivary amylase concentration, and the State-Trait Anxiety Inventory-Form JYZ (STAI-S)

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Device,equipment Other

Interventions/Control_1

Intervention group A is asked to evacuate in the tsunami simulation video after receiving an evacuation order.

Interventions/Control_2

Intervention group B is asked to evacuate in the tsunami simulation video without receiving an evacuation order.

Interventions/Control_3

Control group C walks around in the fantasy simulation video.

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

20 years-old <=

Age-upper limit

50 years-old >

Gender

Male and Female

Key inclusion criteria

(1) Japanese is the mother tongue
(2) Understand the purpose and content of this research, and obtain the necessary consent to participate in the research in writing

Key exclusion criteria

(1) Persons with serious physical illness such as infectious disease, cancer, severe diabetes, or gait disturbance
(2) Persons who are currently being treated for mental illness
(3) Persons who have difficulty understanding Japanese
(4) Persons who are judged to be inappropriate by the principal investigator

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Hiroaki
Middle name
Last name Tomita

Organization

Tohoku University School of Medicine

Division name

Department of Psychiatry

Zip code

980-8574

Address

1-1 Seiryo-machi, Aobaku, Sendai, Miyagi

TEL

022-717-7262

Email

htomita@med.tohoku.ac.jp


Public contact

Name of contact person

1st name Hitomi
Middle name
Last name Usukura

Organization

International Research Institute of Disaster Science, Tohoku University

Division name

Department of Disaster Psychiatry

Zip code

980-8573

Address

2-1 Seiryo-machi, Aobaku, Sendai, Miyagi

TEL

022-717-7897

Homepage URL


Email

usukura@med.tohoku.ac.jp


Sponsor or person

Institute

Tohoku University

Institute

Department

Personal name



Funding Source

Organization

Tohoku 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

Ethics Committee, Graduate School of Medicine

Address

N/A

Tel

N/A

Email

med-kenkyo@grp.tohoku.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

2021 Year 02 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

31

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

2020 Year 04 Month 20 Day

Date of IRB

2020 Year 04 Month 20 Day

Anticipated trial start date

2021 Year 03 Month 08 Day

Last follow-up date

2023 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

2021 Year 02 Month 01 Day

Last modified on

2023 Year 08 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049316


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name