UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000061439 |
|---|---|
| Receipt number | R000070298 |
| Scientific Title | Exploring the neural correlates of cross-modal integration of visual and kinesthetic information in working memory for movement |
| Date of disclosure of the study information | 2026/07/27 |
| Last modified on | 2026/05/01 21:19:15 |
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Basic information
Public title
A functional magnetic resonance imaging study on cross-modal integration of visual and kinesthetic information in working memory for movement
Acronym
An fMRI study on cross-modal integration of visual and kinesthetic information in working memory for movement
Scientific Title
Exploring the neural correlates of cross-modal integration of visual and kinesthetic information in working memory for movement
Scientific Title:Acronym
Neural substrates of sensory information integration in motor working memory
Region
| Japan |
Condition
Condition
Healthy adults
Classification by specialty
| Rehabilitation medicine | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate the neural substrates of kinesthetic and visual information integration in working memory for movement in healthy adults using functional MRI.
Basic objectives2
Others
Basic objectives -Others
To investigate the impact of aging on the neural substrates of kinesthetic and visual information integration in working memory for movement using functional MRI.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Brain activity measured by functional magnetic resonance imaging
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
Prevention
Type of intervention
| Other |
Interventions/Control_1
Working memory tasks
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
| 75 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Healthy acults
Right handed
Key exclusion criteria
Presence or history of any central nervous system disorder
Psychotropic drug use
Lifetime history of substance abuse/dependence
Severe hearing impairment
Severe visual impairment
Upper-extremity amputee
Sensory or motor impairment in the upper extremity
Metal contained within your body
Claustrophobia
Target sample size
80
Research contact person
Name of lead principal investigator
| 1st name | Naofumi |
| Middle name | |
| Last name | Tanaka |
Organization
Saitama Medical University International Medical Center
Division name
Department of Physical Rehabilitation Medicine
Zip code
350-1298
Address
1397-1, Yamane, Hidaka, Saitama, Japan.
TEL
042-984-4111
tanaka-n@med.tohoku.ac.jp
Public contact
Name of contact person
| 1st name | Naofumi |
| Middle name | |
| Last name | Tanaka |
Organization
Saitama Medical University International Medical Center
Division name
Department of Physical Rehabilitation Medicine
Zip code
350-1298
Address
1397-1, Yamane, Hidaka, Saitama, Japan.
TEL
042-984-4111
Homepage URL
tanaka-n@med.tohoku.ac.jp
Sponsor or person
Institute
Saitama Medical University
Institute
Department
Personal name
Funding Source
Organization
Japan Science and Technology Agency
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
Clinical Research Properness Promotion Center, Saitama Medical University International Medical Center
Address
1397-1, Yamane, Hidaka, Saitama, Japan.
Tel
042-984-4523
chikens@saitama-med.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 | 07 | Month | 27 | 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 | 08 | Month | 01 | Day |
Last follow-up date
| 2029 | 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 | 01 | Day |
Last modified on
| 2026 | Year | 05 | Month | 01 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070298
