UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000058950 |
|---|---|
| Receipt number | R000067417 |
| Scientific Title | A study on eye movements, fatigue, and performance during FPS gameplay |
| Date of disclosure of the study information | 2025/09/02 |
| Last modified on | 2025/09/01 10:51:03 |
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Basic information
Public title
A study on eye movements, fatigue, and performance during FPS gameplay
Acronym
Ocular Fatigue and Performance in FPS Games
Scientific Title
A study on eye movements, fatigue, and performance during FPS gameplay
Scientific Title:Acronym
Ocular Fatigue and Performance in FPS Games
Region
| Japan |
Condition
Condition
Fatigue
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To measure eye movements during FPS gameplay, evaluate visual function from the perspective of eye fatigue, and clarify the relationship between eye movements and FPS game performance
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Electrooculography, Eye Movements, Pupil Diameter, Heart Rate, R-R Interval, Electroencephalography, Cognitive Function
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
Educational,Counseling,Training
Type of intervention
| Behavior,custom |
Interventions/Control_1
Participants played the FPS game "VALORANT" and continued until they subjectively felt and reported mental or physical fatigue, or for a maximum duration of three hours, whichever came first.
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
| 18 | years-old | <= |
Age-upper limit
| 45 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Participants must be experienced players of the FPS game "VALORANT".
Had sufficient sleep the night before the experiment.
Avoided excessive alcohol consumption before the experiment.
Avoided caffeine intake on the day of the experiment.
In good health and free from any physical conditions that would interfere with the experiment's execution.
Key exclusion criteria
Currently taking medicine as mydriatics, miotics, antihistamines, antidepressants, or decongestants.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Kaneda |
| Middle name | |
| Last name | Koichi |
Organization
Chiba Institute of Technology
Division name
Faculty of Advanced Engineering
Zip code
275-0023
Address
Shibazono 2-1-1, Narashino-City, Chiba-Pref., Japan
TEL
047-454-9935
koichi.kaneda@p.chibakoudai.jp
Public contact
Name of contact person
| 1st name | Kaneda |
| Middle name | |
| Last name | Koichi |
Organization
Chiba Institute of Technology
Division name
Faculty of Advanced Engineering
Zip code
275-0023
Address
Shibazono 2-1-1, Narashino-City, Chiba-Pref., Japan
TEL
047-454-9935
Homepage URL
koichi.kaneda@p.chibakoudai.jp
Sponsor or person
Institute
Chiba Institute fo Technology
Institute
Department
Personal name
Funding Source
Organization
Foundation for the Fusion Of Science and Technology
Organization
Division
Category of Funding Organization
Non profit foundation
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Human Ethics Committee at the Chiba Institute of Technology
Address
Tsudanuma 2-17-1, Narashino-City, Chiba-Pref., Japan
Tel
047-478-0325
kenkyushien-stf@it-chiba.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
| 2025 | Year | 09 | Month | 02 | 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
| 2025 | Year | 08 | Month | 05 | Day |
Date of IRB
| 2025 | Year | 08 | Month | 05 | Day |
Anticipated trial start date
| 2025 | Year | 09 | Month | 02 | 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
| 2025 | Year | 09 | Month | 01 | Day |
Last modified on
| 2025 | Year | 09 | Month | 01 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067417
