UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000034747
Receipt number R000039624
Scientific Title A neuroimaging study of visual cognition
Date of disclosure of the study information 2018/11/02
Last modified on 2019/09/25 16:00:36

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Basic information

Public title

A neuroimaging study of visual cognition

Acronym

A neuroimaging study of visual cognition

Scientific Title

A neuroimaging study of visual cognition

Scientific Title:Acronym

A neuroimaging study of visual cognition

Region

Japan


Condition

Condition

Normal volunteers

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study aims to examine visual cognition and underlying neural mechanisms using neuroimaging and physiological measurements including MRI, EEG, and eye tracking systems.

Basic objectives2

Bio-availability

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Performance in visual tasks, MRI and EEG data will be examined

Key secondary outcomes



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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

This study contains MRI measurements about 60 min. This procedure meets a definition of "Interventions".

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

40 years-old >

Gender

Male and Female

Key inclusion criteria

A person who has normal or corrected-to-normal vision

Key exclusion criteria

A person who has had brain disease
A person who has had substance dependence
A person who has had psychiatric disorders
A person who has had severe body disease
A person who is pregnant or potentially pregnant
A person who has a pacemaker, metal, or tatoo on his/her body
A person with serious claustrophobia
A person who is regarded as ineligible for participation by a researcher /doctor

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Makiko
Middle name
Last name Yamada

Organization

National Institutes for Quantum and Radiological Science and Technology

Division name

Department of Functional Brain Imaging Research

Zip code

263-8555

Address

4-9-1 Anagawa, Inage-ku, Chiba

TEL

043-206-3425

Email

yamada.makiko@qst.go.jp


Public contact

Name of contact person

1st name Kazuhisa
Middle name
Last name Shibata

Organization

National Institutes for Quantum and Radiological Science and Technology

Division name

Department of Functional Brain Imaging Research

Zip code

263-8555

Address

4-9-1 Anagawa, Inage-ku, Chiba

TEL

043-206-3425

Homepage URL


Email

shibata.kazuhisa@qst.go.jp


Sponsor or person

Institute

National Institutes for Quantum and Radiological Science and Technology

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology

Address

4-9-1 Anagawa, Inage, Chiba

Tel

043-206-4706

Email

helsinki@qst.go.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

2018 Year 11 Month 02 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

2

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

Terminated

Date of protocol fixation

2018 Year 10 Month 31 Day

Date of IRB

2018 Year 10 Month 31 Day

Anticipated trial start date

2019 Year 09 Month 17 Day

Last follow-up date

2019 Year 09 Month 25 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 11 Month 02 Day

Last modified on

2019 Year 09 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039624


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name