UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056174
Receipt number R000064188
Scientific Title Effects of light exposure that has less stimulation on intrinsically photosensitive retinal ganglion cells(ipRGCs) and keeps color rendering property during night on human circadian rhythms
Date of disclosure of the study information 2025/01/01
Last modified on 2024/11/17 23:21:19

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Basic information

Public title

Effects of light exposure that has less stimulation on intrinsically photosensitive retinal ganglion cells(ipRGCs) and keeps color rendering property during night on human circadian rhythms

Acronym

Effects of light exposure that has less stimulation on intrinsically photosensitive retinal ganglion cells(ipRGCs) and keeps color rendering property during night on human circadian rhythms

Scientific Title

Effects of light exposure that has less stimulation on intrinsically photosensitive retinal ganglion cells(ipRGCs) and keeps color rendering property during night on human circadian rhythms

Scientific Title:Acronym

Effects of light exposure that has less stimulation on intrinsically photosensitive retinal ganglion cells(ipRGCs) and keeps color rendering property during night on human circadian rhythms

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To determine how the light that has less stimulation on ipRGCs and keeps color rendering property during night affect human circadian rhythm.

Basic objectives2

Others

Basic objectives -Others

To determine how the light that has less stimulation on ipRGCs and keeps color rendering property during night affect human circadian rhythm.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sleep efficiency

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Light that has less stimulation on ipRGCs

Interventions/Control_2

General LED light

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

39 years-old >=

Gender

Male

Key inclusion criteria

Since the purpose is to collect the basic data, the study will be conducted with adults, not the elderly.

Key exclusion criteria

(1) Patients with a result score of 3 or 4 on the Cornell Medical Index for neurosis emotional disorders
(2) The score of Morningness Eveningness Questionnaire is 70 or more(extreme morning person) or 30 or less(extreme night person)
(3) Pittsburgh Sleep Questionnaire with a score of 6 or higher
(4) Those who have had a change in their living hours due to shift work or travel to time zones within one month
(5) Those who are taking any oral medication or smoking
(6) Those who has color vision variation
(7) Dark-adapted pupil size is out of range of 5.72 plus or minus 1.19 mm(mean plus or minus 3SD)
(8) Students who are currently enrolled or may be enrolled in a course that the principal investigator is taking

Target sample size

35


Research contact person

Name of lead principal investigator

1st name Tomoko
Middle name
Last name Wakamura

Organization

Kyoto University

Division name

School of Human Health Sciences, Graduate School of Medicine

Zip code

606-8507

Address

53, Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

81-75-751-3974

Email

wakamura.tomoko.5v@kyoto-u.ac.jp


Public contact

Name of contact person

1st name Tomoko
Middle name
Last name Wakamura

Organization

Kyoto University

Division name

School of Human Health Sciences, Graduate School of Medicine

Zip code

606-8507

Address

53, Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

81-75-751-3974

Homepage URL


Email

wakamura.tomoko.5v@kyoto-u.ac.jp


Sponsor or person

Institute

Kyoto University

Institute

Department

Personal name



Funding Source

Organization

Kyoto 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

Kyoto University Graduate School and Faculty of Medicine, Ethics Committee

Address

Konoe-cho, Sakyo-ku, Kyoto

Tel

075-753-4680

Email

ethcom@kuhp.kyoto-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

2025 Year 01 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

2024 Year 12 Month 31 Day

Date of IRB


Anticipated trial start date

2024 Year 12 Month 31 Day

Last follow-up date

2025 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

2024 Year 11 Month 17 Day

Last modified on

2024 Year 11 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064188