UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000059365
Receipt number R000067899
Scientific Title HAIR-Q Study study: Hair and Questionnaire-based Diabetes Screening Study
Date of disclosure of the study information 2025/12/22
Last modified on 2026/02/12 10:54:11

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Basic information

Public title

A Novel Diabetes Screening Approach Combining Simple Questions and Hair Analysis

Acronym

HAIR-Q Study: Hair and Questionnaire-based Diabetes Screening Study

Scientific Title

HAIR-Q Study study: Hair and Questionnaire-based Diabetes Screening Study

Scientific Title:Acronym

HAIR-Q Study

Region

Japan


Condition

Condition

diabetes

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to develop a diabetes screening method in beauty salons.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

This study aims to develop a method for diabetes screening (early detection) in beauty salons. A questionnaire survey and measurement of glycated proteins in hair will be conducted to examine the feasibility of simple diabetes screening in this familiar setting.

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

20 years-old <=

Age-upper limit

70 years-old >

Gender

Male and Female

Key inclusion criteria

Aged 20 years or older and under 70 years.

Key exclusion criteria

Individuals who cannot use the web

Individuals without hair

Individuals deemed unsuitable for participation in this study by the principal investigator or co-investigators

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Naoki
Middle name
Last name Sakane

Organization

National Hospital Organization Kyoto Medical Center

Division name

Clinical Research Institute

Zip code

612-8555

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto

TEL

0756419161

Email

404-j-doit1@mail.hosp.go.jp


Public contact

Name of contact person

1st name Masayuki
Middle name
Last name Domichi

Organization

National Hospital Organization Kyoto Medical Center

Division name

Clinical Research Institute

Zip code

612-8555

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto

TEL

0756419161

Homepage URL


Email

404-j-doit1@mail.hosp.go.jp


Sponsor or person

Institute

National Hospital Organization Kyoto Medical Center

Institute

Department

Personal name



Funding Source

Organization

National Hospital Organization Kyoto Medical Center

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Hospital Organization Kyoto Medical Center

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto, Japan.

Tel

0756419161

Email

404-j-doit1@mail.hosp.go.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 12 Month 22 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

Open public recruiting

Date of protocol fixation

2025 Year 11 Month 17 Day

Date of IRB

2025 Year 12 Month 22 Day

Anticipated trial start date

2026 Year 01 Month 16 Day

Last follow-up date

2028 Year 12 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Observational study


Management information

Registered date

2025 Year 10 Month 10 Day

Last modified on

2026 Year 02 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067899