UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000061558 |
|---|---|
| Receipt number | R000070437 |
| Scientific Title | Evaluation of electric field intensity in the primary somatosensory cortex using simNIBS analysis based on individual MRI data. |
| Date of disclosure of the study information | 2026/05/13 |
| Last modified on | 2026/05/13 19:10:36 |
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Basic information
Public title
Evaluation of electric field intensity in the primary somatosensory cortex using simNIBS analysis based on individual MRI data.
Acronym
Evaluation of electric field intensity in the primary somatosensory cortex using simNIBS analysis based on individual MRI data.
Scientific Title
Evaluation of electric field intensity in the primary somatosensory cortex using simNIBS analysis based on individual MRI data.
Scientific Title:Acronym
Evaluation of electric field intensity in the primary somatosensory cortex using simNIBS analysis based on individual MRI data.
Region
| Japan |
Condition
Condition
healthy persons
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
to investigate the electric field intensity generated in the primary somatosensory cortex by transcranial electrical stimulation, taking into account individual brain structures.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Electric field intensity as simulated using simNIBS
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Non-randomized
Randomization unit
Blinding
Single blind -participants are blinded
Control
Dose comparison
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Transcranial electrical stimulation (electrode placement: C3, P3)
Interventions/Control_2
Transcranial electrical stimulation (electrode placement: CP3, Fp2)
Interventions/Control_3
High definition transcranial electrical stimulation
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
| 18 | years-old | <= |
Age-upper limit
| 25 | years-old | > |
Gender
Male and Female
Key inclusion criteria
healthy persons at aged 18-25 y.o.
Key exclusion criteria
metal implants in your body, an implanted medical device (such as a pacemaker) listed on the MRI questionnaire, less than one month since your surgery, or pregnant
Target sample size
50
Research contact person
Name of lead principal investigator
| 1st name | Kei |
| Middle name | |
| Last name | Saito |
Organization
Niigata University of Health and Welfare
Division name
Institute for Human Movement and Medical Sciences
Zip code
9503198
Address
1398 Shimami-cho, Kita-ku, Niigata City, Niigata
TEL
0252501954
kei-saito@nuhw.ac.jp
Public contact
Name of contact person
| 1st name | Kei |
| Middle name | |
| Last name | Saito |
Organization
Niigata University of Health and Welfare
Division name
Institute for Human Movement and Medical Sciences
Zip code
9503198
Address
1398 Shimami-cho, Kita-ku, Niigata City, Niigata
TEL
0252501954
Homepage URL
kei-saito@nuhw.ac.jp
Sponsor or person
Institute
Niigata University of Health and Welfare
Institute
Department
Personal name
Funding Source
Organization
Niigata University of Health and Welfare
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
Ethics Committee, Niigata University of Health and Welfare
Address
1398 Shimami-cho, Kita-ku, Niigata-shi, Niigata
Tel
025-257-4455
rinri@nuhw.ac.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
| 2026 | Year | 05 | Month | 13 | 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
| 2026 | Year | 05 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2026 | Year | 06 | Month | 10 | Day |
Last follow-up date
| 2028 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2026 | Year | 05 | Month | 13 | Day |
Last modified on
| 2026 | Year | 05 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070437
