UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054759
Receipt number R000062578
Scientific Title Accessibility Survey for the Visually Impaired (Main Survey)- Usability survey of Eye Navi Nishi-Chiba Campus specifications -
Date of disclosure of the study information 2024/06/27
Last modified on 2024/12/24 13:10:10

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Accessibility Survey for the Visually Impaired (Main Survey)- Usability survey of Eye Navi Nishi-Chiba Campus specifications -

Acronym

Accessibility Survey for the Visually Impaired (Main Survey)- Usability survey of Eye Navi Nishi-Chiba Campus specifications -

Scientific Title

Accessibility Survey for the Visually Impaired (Main Survey)- Usability survey of Eye Navi Nishi-Chiba Campus specifications -

Scientific Title:Acronym

Nishi-Chiba Eye Navi

Region

Japan


Condition

Condition

visually impaired person

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The vast Nishi-Chiba Campus, the headquarters of Chiba University, is not designed for the visually impaired. The surrounding area is well-equipped with Braille blocks. Chiba University, which is committed to diversity, needs to create a campus environment that is friendly to the visually impaired. However, the development of infrastructure requires a huge budget. Therefore, using the existing "EyeNavi" mobility support application for the visually impaired, we set up a flow line from the West Chiba Station ticket gate to the entrance of the Faculty of Education Building No. 4 via the South Gate, and asked visually impaired people to use it and confirm its practicality. The purpose of this project is not for development, but to confirm the usability.

Basic objectives2

Others

Basic objectives -Others

tolerability

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

usability

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

80 years-old >

Gender

Male and Female

Key inclusion criteria

Visually impaired (those who cannot move without a white cane)

Key exclusion criteria

Persons with some other functional disability

Target sample size

3


Research contact person

Name of lead principal investigator

1st name Takeshi
Middle name
Last name Sugawara

Organization

Chiba University Hospital

Division name

Ophthalmology

Zip code

2630024

Address

Chiba City, Chuo-ku, Inohana 1-8-1

TEL

0432262484

Email

takeshis@faculty.chiba-u.jp


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Sugawara

Organization

Chiba University Hospital

Division name

Ophthalmology

Zip code

2630024

Address

Chiba City, Chuo-ku, Inohana 1-8-1

TEL

0432262484

Homepage URL


Email

takeshis@faculty.chiba-u.jp


Sponsor or person

Institute

Chiba University Hospital

Institute

Department

Personal name



Funding Source

Organization

Chiba University Hospital

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

Chiba University Hospital

Address

Chiba City, Chuo-ku, Inohana 1-8-1

Tel

0432227171

Email

takeshis@faculty.chiba-u.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

2024 Year 06 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

3

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

Completed

Date of protocol fixation

2024 Year 04 Month 16 Day

Date of IRB

2024 Year 06 Month 24 Day

Anticipated trial start date

2024 Year 07 Month 01 Day

Last follow-up date

2024 Year 12 Month 12 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Create a walking support application for the visually impaired, Eye Navi Nishi-Chiba Campus limited mode, and have visually impaired people use it and provide feedback.


Management information

Registered date

2024 Year 06 Month 25 Day

Last modified on

2024 Year 12 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062578