UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000057410 |
|---|---|
| Receipt number | R000065592 |
| Scientific Title | Creating easy-to-notice and low-stress signal sounds based on biological rhythms |
| Date of disclosure of the study information | 2025/05/01 |
| Last modified on | 2025/03/26 16:06:50 |
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Basic information
Public title
Creating easy-to-notice and low-stress signal sounds based on biological rhythms
Acronym
Creating easy-to-notice and low-stress signal sounds based on biological rhythms
Scientific Title
Creating easy-to-notice and low-stress signal sounds based on biological rhythms
Scientific Title:Acronym
Creating easy-to-notice and low-stress signal sounds based on biological rhythms
Region
| Japan |
Condition
Condition
Healty adult men
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to clarify the differences in physiological responses of subjects to sounds under certain conditions throughout their daily lives.
Basic objectives2
Others
Basic objectives -Others
The purpose of this study is to clarify the differences in physiological responses of subjects to sounds under certain conditions throughout their daily lives.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Heart rate variability
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
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
Prevention
Type of intervention
| Other |
Interventions/Control_1
Start time: 8:00
Interventions/Control_2
Start time: 16:00
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
This study is performed on adults with no history of hearing problems.
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) 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
wakamura.tomoko.5v@kyoto-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
wakamura.tomoko.5v@kyoto-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
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 | 05 | 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
22
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
| 2017 | Year | 11 | Month | 02 | Day |
Date of IRB
| 2019 | Year | 04 | Month | 01 | Day |
Anticipated trial start date
| 2019 | Year | 04 | Month | 20 | Day |
Last follow-up date
| 2019 | Year | 08 | Month | 31 | Day |
Date of closure to data entry
| 2019 | Year | 08 | Month | 31 | Day |
Date trial data considered complete
| 2019 | Year | 09 | Month | 20 | Day |
Date analysis concluded
| 2023 | Year | 11 | Month | 30 | Day |
Other
Other related information
Management information
Registered date
| 2025 | Year | 03 | Month | 26 | Day |
Last modified on
| 2025 | Year | 03 | Month | 26 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065592
