UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016767
Receipt number R000019454
Scientific Title The study of the influence of voluntary movement to the aftereffects of repetitive transcranial magnetic stimulation
Date of disclosure of the study information 2015/03/10
Last modified on 2016/09/28 14:16:04

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Basic information

Public title

The study of the influence of voluntary movement to the aftereffects of repetitive transcranial magnetic stimulation

Acronym

The study of the influence of voluntary movement to the aftereffects of repetitive transcranial magnetic stimulation

Scientific Title

The study of the influence of voluntary movement to the aftereffects of repetitive transcranial magnetic stimulation

Scientific Title:Acronym

The study of the influence of voluntary movement to the aftereffects of repetitive transcranial magnetic stimulation

Region

Japan


Condition

Condition

healthy volunteers

Classification by specialty

Neurology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to resolve how the voluntary movements effect the aftereffects of the rTMS

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

the excitability of the motor cortex

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Maneuver

Interventions/Control_1

the subjects do voluntary movements after QPS application

Interventions/Control_2

QPS alone

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

24 years-old <=

Age-upper limit

70 years-old >=

Gender

Male and Female

Key inclusion criteria

medical doctors who know TMS

Key exclusion criteria

epilepsy, mental illness, CVD

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yoshikazu Ugawa

Organization

Fukushima Medical University

Division name

the department of neurology

Zip code


Address

1 Hikarigaoka, Fukushima, Japan

TEL

024-547-1111

Email

ugawa-tky@umin.net


Public contact

Name of contact person

1st name
Middle name
Last name Suguru Kadowaki

Organization

Fukushima Medical University

Division name

the department of neurology

Zip code


Address

1 Hikarigaoka, Fukushima, Japan

TEL

024-547-1111

Homepage URL


Email

skado@fmu.ac.jp


Sponsor or person

Institute

Fukushima Medical University

Institute

Department

Personal name



Funding Source

Organization

self funding

Organization

Division

Category of Funding Organization

Self funding

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



Other administrative information

Date of disclosure of the study information

2015 Year 03 Month 10 Day


Related information

URL releasing protocol


Publication of results

Published


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

Completed

Date of protocol fixation

2012 Year 06 Month 22 Day

Date of IRB


Anticipated trial start date

2012 Year 06 Month 22 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

2015 Year 03 Month 10 Day

Last modified on

2016 Year 09 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019454