UMIN-CTR Clinical Trial

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

Name:
UMIN ID:

Recruitment status Preinitiation
Unique ID issued by UMIN UMIN000023526
Receipt No. R000027097
Scientific Title Neural mechanism of behavioral and neurophysiological changed by sensorimotor incongruence.
Date of disclosure of the study information 2016/08/07
Last modified on 2016/08/07

* 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 Neural mechanism of behavioral and neurophysiological changed by sensorimotor incongruence.
Acronym Neural mechanism of behavioral and neurophysiological changed by sensorimotor incongruence.
Scientific Title Neural mechanism of behavioral and neurophysiological changed by sensorimotor incongruence.
Scientific Title:Acronym Neural mechanism of behavioral and neurophysiological changed by sensorimotor incongruence.
Region
Japan

Condition
Condition Healthy subjects
Classification by specialty
Orthopedics Rehabilitation medicine Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 Pathological pain and dysesthesia are caused by sensorimotor incongruence. However, it is still not clear that behavioral and neurophysiological changes caused by sensorimotor incongruence. In the present study, we clarify the neural mechanism of behavioral and neurophysiological changes using electroencephalogram.
Basic objectives2 Others
Basic objectives -Others Pathological pain and dysesthesia are caused by sensorimotor incongruence. However, it is still not clear that behavioral and neurophysiological changes caused by sensorimotor incongruence. In the present study, we clarify the neural mechanism of behavioral and neurophysiological changes using electroencephalogram.
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes dysesthesia
range of motion
muscle activity
Key secondary outcomes

Base
Study type Interventional

Study design
Basic design Parallel
Randomization Non-randomized
Randomization unit
Blinding Open -no one is blinded
Control Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 4
Purpose of intervention Treatment
Type of intervention
Other
Interventions/Control_1 Bimanual coordination task.
Mirror congruence condition.
Interventions/Control_2 Bimanual coordination task.
Mirror incongruence condition.
Interventions/Control_3 Bimanual coordination task.
Board congruence condition.
Interventions/Control_4 Bimanual coordination task.
Board incongruence condition.
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10

Eligibility
Age-lower limit
18 years-old <
Age-upper limit
60 years-old >
Gender Male and Female
Key inclusion criteria Participants had no current or past physical or mental illness (e.g., neurological disorders or chronic pain) and normal or corrected-to-normal vision. Demographic details including occupation and a brief medical history including hand dominance was obtained for all subjects.
Key exclusion criteria neurological disorders or chronic pain
Target sample size 30

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Osamu Katayama
Organization Graduate School of Health Sciences, Kio University
Division name Department of Neurorehabilitation
Zip code
Address 4-2-2 Umami-naka, Koryo-cho, Kitakatsuragi-gun, Nara, 635-0832, Japan.
TEL +81745541603
Email 609.sam@gmail.com

Public contact
Name of contact person
1st name
Middle name
Last name Osamu Katayama
Organization Graduate School of Health Sciences, Kio University
Division name Department of Neurorehabilitation
Zip code
Address 4-2-2 Umami-naka, Koryo-cho, Kitakatsuragi-gun, Nara, 635-0832, Japan.
TEL +81745541603
Homepage URL
Email 609.sam@gmail.com

Sponsor
Institute Kio University
Institute
Department

Funding Source
Organization Kio University
Organization
Division
Category of Funding Organization Other
Nationality of Funding Organization Japan

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
2016 Year 08 Month 07 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 Preinitiation
Date of protocol fixation
2016 Year 08 Month 31 Day
Date of IRB
Anticipated trial start date
2016 Year 09 Month 30 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 08 Month 07 Day
Last modified on
2016 Year 08 Month 07 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027097

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.