UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000062422
Receipt number R000071444
Scientific Title Follow-up interview study on perceptions of the impact of daily alcohol consumption and acceptability of digital support
Date of disclosure of the study information 2026/08/31
Last modified on 2026/07/31 14:43:52

* 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

Follow-up interview study on perceptions of the impact of daily alcohol consumption and acceptability of digital support

Acronym

Follow-up interview study on perceptions of the impact of daily alcohol consumption and acceptability of digital support

Scientific Title

Follow-up interview study on perceptions of the impact of daily alcohol consumption and acceptability of digital support

Scientific Title:Acronym

Follow-up interview study on perceptions of the impact of daily alcohol consumption and acceptability of digital support

Region

Japan


Condition

Condition

Healthy subjects

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study will be conducted to examine perceptions of the effects of alcohol consumption on sleep, physical condition, work performance, and other aspects of daily life, as well as the acceptability of, trust in, and concerns about digital support technologies.

Basic objectives2

Others

Basic objectives -Others

Qualitative interview study on perceptions, acceptability, and concerns regarding digital support

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Qualitative themes regarding perceptions of the effects of alcohol consumption on sleep, physical condition, work, etc., and acceptability, trust, concerns, etc. regarding digital support technology

Key secondary outcomes

Qualitative themes regarding conditions under which behavioral changes may occur and factors hindering them


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

20 years-old <=

Age-upper limit

40 years-old >

Gender

Male and Female

Key inclusion criteria

1. Persons who participated in the relevant prior study
2. Persons who have received a sufficient explanation regarding the purpose and contents of this study, have the capacity to give informed consent, can understand the details well, and give their own consent via electronic informed consent

Key exclusion criteria

1. Persons who did not participate in the relevant prior study

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Takahiro
Middle name
Last name Masuda

Organization

Asahi Quality & Innovations, Ltd.

Division name

Next Beverage Laboratories

Zip code

302-0106

Address

1-21, Midori 1-chome, Moriya-shi, Ibaraki, Japan

TEL

0297-46-1111

Email

takahiro.masuda@asahi-qi.co.jp


Public contact

Name of contact person

1st name Ayumi
Middle name
Last name Sugioka

Organization

Macromill Carenet, Inc.

Division name

Clinical Research Solution Division

Zip code

108-0075

Address

Shinagawa East One Tower 11F, 2-16-1 Konan, Minato-ku, Tokyo, Japan

TEL

03-6716-7108

Homepage URL


Email

umin_info@macromillcarenet.jp


Sponsor or person

Institute

Macromill Carenet, Inc.

Institute

Department

Personal name



Funding Source

Organization

Asahi Quality & Innovations, Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethical Committee of Kobuna Orthopedics Clinic

Address

311-2 Joto-machi, Maebashi-shi, Gumma

Tel

027-212-5608

Email

sagawa@mc-connect.co.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

2026 Year 08 Month 31 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 30 Day

Date of IRB

2026 Year 07 Month 30 Day

Anticipated trial start date

2026 Year 07 Month 31 Day

Last follow-up date

2026 Year 08 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 07 Month 31 Day

Last modified on

2026 Year 07 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071444