UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024799
Receipt number R000028533
Scientific Title The sensory stimuli induced hemodynamic responses in the cerebral cortex during the rehabilitative task
Date of disclosure of the study information 2016/11/16
Last modified on 2016/11/11 12:29:05

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Basic information

Public title

The sensory stimuli induced hemodynamic responses in the cerebral cortex during the rehabilitative task

Acronym

The sensory stimuli induced cortical responses

Scientific Title

The sensory stimuli induced hemodynamic responses in the cerebral cortex during the rehabilitative task

Scientific Title:Acronym

The sensory stimuli induced cortical responses

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the sensory stimuli induced cortical hemodynamic responses during the rehabilitative motor task.

Basic objectives2

Bio-availability

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

The hemodynamic responses by the near-infrared spectroscopy

Key secondary outcomes

The results of motor task and the subjective assessment of sensory stimuli


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is considered as a block.

Blocking

NO

Concealment

Pseudo-randomization


Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Behavior,custom

Interventions/Control_1

The sensory stimuli during the motor task

Interventions/Control_2

The pseudo sensory stimuli during the motor task

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

29 years-old >=

Gender

Male and Female

Key inclusion criteria

(1) healthy adults (20-29 years-old)
(2) voluntary participation by signboard
(3) obtaining the informed consent following the understanding of the research

Key exclusion criteria

(1) patient with orthopedic diseases or sensory dysfunctions related to the task-difficulties
(2) diagnosis experience of psychiatry or neurology
(3) student belonging to the researcher's class
(4) judgement of unsuitable by the principal investigator or researcher

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Urakawa Susumu

Organization

Hiroshima Univ

Division name

Dept of Musculoskeletal Functional Research and Regeneration

Zip code


Address

1-2-3, Kasumi, Minami-ku, Hiroshima

TEL

082-257-5430

Email

urkawas@hiroshima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Urakawa Susumu

Organization

Hiroshima Univ

Division name

Dept of Musculoskeletal Functional Research and Regeneration

Zip code


Address

1-2-3, Kasumi, Minami-ku, Hiroshima

TEL

082-257-5430

Homepage URL


Email

urkawas@hiroshima-u.ac.jp


Sponsor or person

Institute

Hiroshima Univ

Institute

Department

Personal name



Funding Source

Organization

Hiroshima Univ

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


Address


Tel


Email



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

広島大学


Other administrative information

Date of disclosure of the study information

2016 Year 11 Month 16 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

Enrolling by invitation

Date of protocol fixation

2016 Year 11 Month 11 Day

Date of IRB


Anticipated trial start date

2016 Year 11 Month 11 Day

Last follow-up date


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 11 Day

Last modified on

2016 Year 11 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028533


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name