UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Open public recruiting
Unique ID issued by UMIN UMIN000036806
Receipt No. R000041881
Scientific Title Elucidation of neural basis underlying individual difference in spatial orientation
Date of disclosure of the study information 2019/05/25
Last modified on 2019/05/21

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title Elucidation of neural basis underlying individual difference in spatial orientation
Acronym Neural basis underlying spatial orientation
Scientific Title Elucidation of neural basis underlying individual difference in spatial orientation
Scientific Title:Acronym Neural basis underlying spatial orientation
Region
Japan

Condition
Condition Healthy adult
Classification by specialty
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 The purpose of this study is to elucidate the neural basis involved in the individual difference in spatial orientation
Basic objectives2 Others
Basic objectives -Others To assess the effect of visual background on the spatial orientation
Trial characteristics_1 Confirmatory
Trial characteristics_2 Others
Developmental phase

Assessment
Primary outcomes Subjective visual vertical (SVV)
Subjective visual body axis (SVBA)
Key secondary outcomes MRI image (T1 and T2)

Base
Study type Interventional

Study design
Basic design Single arm
Randomization Non-randomized
Randomization unit
Blinding Open -no one is blinded
Control Self control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 1
Purpose of intervention Educational,Counseling,Training
Type of intervention
Device,equipment
Interventions/Control_1 Head MRI (T1 and T2)
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
20 years-old <=
Age-upper limit
60 years-old >
Gender Male and Female
Key inclusion criteria 1. Individuals without a neurological or psychiatric history
2. Right handedness
3. Capability of informed consent based on their own decision
Key exclusion criteria 1. Individuals with a history of head trauma
2. Individuals with a history of organic brain and spinal disease
3. Individuals with a history or organic vestibular disease
4. Individuals who have a history of disorders of consciousness and/or seizure
5. Individuals with dizziness and strong motion sickness
6. Individuals who are unable to undergo MRI
7. Individuals that researchers decide that they are inappropriate for study participation
Target sample size 50

Research contact person
Name of lead principal investigator
1st name Satoshi
Middle name
Last name Tanaka
Organization Hamamatsu University School of Medicine
Division name Psychology
Zip code 431-3192
Address 1-20-1 Handayama Higashi-ku, Hamamatsu-city, Japan
TEL 053-453-2387
Email tanakas@hama-med.ac.jp

Public contact
Name of contact person
1st name Satoshi
Middle name
Last name Tanaka
Organization Hamamatsu University School of Medicine
Division name Psychology
Zip code 431-3192
Address 1-20-1 Handayama Higashi-ku, Hamamatsu-city, Japan
TEL 053-453-2387
Homepage URL
Email tanakas@hama-med.ac.jp

Sponsor
Institute Hamamatsu University School od Medicine
Institute
Department

Funding Source
Organization Hamamatsu University School of Medichine
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 Hamamatsu University School of Medicine
Address 1-20-1 Handayama Higashi-ku, Hamamatsu-city, Japan
Tel 0534532850
Email quality@hama-med.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
2019 Year 05 Month 25 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
2019 Year 02 Month 10 Day
Date of IRB
2019 Year 05 Month 15 Day
Anticipated trial start date
2019 Year 05 Month 20 Day
Last follow-up date
2021 Year 05 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
2019 Year 05 Month 21 Day
Last modified on
2019 Year 05 Month 21 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041881

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.