UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000063622 |
|---|---|
| Receipt number | R000072815 |
| Scientific Title | A Study on the Concurrent Presentation of Optokinetic Stimuli and Tasks in Healthy Individuals |
| Date of disclosure of the study information | 2026/11/13 |
| Last modified on | 2026/11/13 14:40:11 |
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Basic information
Public title
A Study on the Concurrent Presentation of Optokinetic Stimuli and Tasks in Healthy Individuals
Acronym
Research on optokinetic stimuli
Scientific Title
A Study on the Concurrent Presentation of Optokinetic Stimuli and Tasks in Healthy Individuals
Scientific Title:Acronym
Research on optokinetic stimuli
Region
| Japan |
Condition
Condition
Healthy young adults
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study aims to investigate whether an intervention known as "optokinetic stimulation"-which is considered effective for hemispatial neglect, a condition that can occur following a stroke-remains effective when administered concurrently with other tasks, rather than in isolation as has traditionally been the case.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
apple test, line bisection test, bell test
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -participants are blinded
Control
Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Performing a task (assembling blocks to create a structure) concurrently with the presentation of optokinetic stimuli.
Interventions/Control_2
Do not perform other tasks while the optokinetic stimulus is being presented.
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
| 18 | years-old | <= |
Age-upper limit
| 23 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Healthy young adults
Key exclusion criteria
Individuals with a history of central nervous system disorders. Individuals who are left-handed.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Akifumi |
| Middle name | |
| Last name | Komura |
Organization
Seijoh University
Division name
Fuculty of Rehabilitation
Zip code
476-8588
Address
2-172 Fukinodai, Tokai city, Aichi, Japan
TEL
0526016000
koumura@seijoh-u.ac.jp
Public contact
Name of contact person
| 1st name | Akifumi |
| Middle name | |
| Last name | Komura |
Organization
Seijoh University
Division name
Fuculty of Rehabilitation
Zip code
476-8588
Address
2-172 Fukinodai, Tokai city, Aichi, Japan
TEL
0526016000
Homepage URL
koumura@seijoh-u.ac.jp
Sponsor or person
Institute
Seijoh University
Institute
Department
Personal name
Funding Source
Organization
Seijoh University
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
Seijoh University
Address
2-172 Fukinodai, Tokai city, Aichi, Japan
Tel
0526016000
kenkyu-entry@seijoh-u.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 | 11 | 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
Enrolling by invitation
Date of protocol fixation
| 2026 | Year | 10 | Month | 21 | Day |
Date of IRB
| 2026 | Year | 10 | Month | 21 | Day |
Anticipated trial start date
| 2026 | Year | 11 | Month | 13 | Day |
Last follow-up date
| 2027 | 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 | 11 | Month | 13 | Day |
Last modified on
| 2026 | Year | 11 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072815
