UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000062058 |
|---|---|
| Receipt number | R000071009 |
| Scientific Title | A Study on Effective Signage for Facilitating AED Location |
| Date of disclosure of the study information | 2026/07/01 |
| Last modified on | 2026/06/25 18:29:15 |
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Basic information
Public title
A Study on Effective Signage for Facilitating AED Location
Acronym
A Study on Effective Signage for Facilitating AED Location
Scientific Title
A Study on Effective Signage for Facilitating AED Location
Scientific Title:Acronym
A Study on Effective Signage for Facilitating AED Location
Region
| Japan |
Condition
Condition
N/A
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the most effective signage for facilitating the location of AED.
Basic objectives2
Others
Basic objectives -Others
To evaluate which types of information on signage most effectively facilitate the location of AED.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The time from viewing the signage to locating the target object and returning to the starting point (point A).
Key secondary outcomes
The signage that was remembered as the most memorable by the participant.
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
Numbered container method
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Other |
Interventions/Control_1
Participants will be instructed to view signage presented at a designated location, search for a target object, and return to the starting point with the object. Three different types of signage will be used, each corresponding to a target object placed at an equal distance from the starting point. For each condition, the time required to locate the target object and return to the starting point will be measured.
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
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Participants will consist of students and staff affiliated with University A.
Key exclusion criteria
Participants must be healthy adults with no relevant medical history and not be pregnant.
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | AYAKO |
| Middle name | |
| Last name | FUKUSHIMA |
Organization
Hokkaido University of Science
Division name
Faculty of health science, department of nursing
Zip code
006-8585
Address
15-4-1, Maeda 7-jo, Teine-ku, Sapporo-shi, Hokkaido, Japan
TEL
011-681-2161
fukushima-ay@hus.ac.jp
Public contact
Name of contact person
| 1st name | AYAKO |
| Middle name | |
| Last name | FUKUSHIMA |
Organization
Hokkaido university of science
Division name
Faculty of health science, department of nursing
Zip code
006-8585
Address
15-4-1, Maeda 7-jo, Teine-ku, Sapporo-shi, Hokkaido, Japan
TEL
011-681-2161
Homepage URL
fukushima-ay@hus.ac.jp
Sponsor or person
Institute
Hokkaido University of Science
Institute
Department
Personal name
Funding Source
Organization
Hokkaido University of Science
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
Hokkaido university of science
Address
15-4-1, Maeda 7-jo, Teine-ku, Sapporo-shi, Hokkaido, Japan
Tel
011-681-2161
fukushima-ay@hus.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
北海道
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 07 | Month | 01 | 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 | 07 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2026 | Year | 07 | Month | 31 | 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 | 06 | Month | 25 | Day |
Last modified on
| 2026 | Year | 06 | Month | 25 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000071009
