UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024681
Receipt number R000028397
Scientific Title Examination of the neural basis of the visuoperceptual function
Date of disclosure of the study information 2016/11/03
Last modified on 2020/11/05 11:43:33

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Basic information

Public title

Examination of the neural basis of the visuoperceptual function

Acronym

Examination of the neural basis of the visuoperceptual function

Scientific Title

Examination of the neural basis of the visuoperceptual function

Scientific Title:Acronym

Examination of the neural basis of the visuoperceptual function

Region

Japan


Condition

Condition

Healthy individuals

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate the neural basis of visuoperceptual function.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The correlation between the change of BOLD signals, the change of electroencephalogram and the psychological changes

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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Behavior,custom

Interventions/Control_1

1. Psychological test: 30min
2. MRI/EEG scan: 130min (including preparation and explanation)
Break time
3. MRI/EEG scan: 30min (including preparation and explanation)
4. Psychological test: 65min

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

Healthy individuals who have the ability to provide informed consent.

Key exclusion criteria

Psychiatric disorders including drug dependence
Serious medical illness

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Yamada
Middle name
Last name Makiko

Organization

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

Division name

Department of Functional Brain Imaging Research

Zip code

263-8555

Address

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

TEL

043-206-3251

Email

yamada.makiko@qst.go.jp


Public contact

Name of contact person

1st name Haruki
Middle name
Last name Nishimura

Organization

National Institute of Radiological Sciences

Division name

Department of Functional Brain Imaging Research

Zip code

263-8555

Address

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

TEL

043-206-3025

Homepage URL


Email

nishimura.haruki@qst.go.jp


Sponsor or person

Institute

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

Institute

Department

Personal name



Funding Source

Organization

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

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

Certified Review Board

Address

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

Tel

043-206-4709

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

2016 Year 11 Month 03 Day


Related information

URL releasing protocol

https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000028397

Publication of results

Unpublished


Result

URL related to results and publications

https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000028397

Number of participants that the trial has enrolled

30

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

The results of this study are not published.

Date of the first journal publication of results


Baseline Characteristics

Healthy individuals

Participant flow

The data of all participants were analyzed.

Adverse events

None

Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2016 Year 10 Month 28 Day

Date of IRB

2016 Year 10 Month 28 Day

Anticipated trial start date

2016 Year 11 Month 02 Day

Last follow-up date

2017 Year 08 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 11 Month 02 Day

Last modified on

2020 Year 11 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028397


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name