UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000059007
Receipt number R000067483
Scientific Title Research on the effects of fermentable dietary fiber and behavioral intervention on the skin
Date of disclosure of the study information 2025/09/05
Last modified on 2025/09/05 15:02:16

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Basic information

Public title

Research on the effects of fermentable dietary fiber and behavioral intervention on the skin

Acronym

Research on the effects of fermentable dietary fiber and behavioral intervention on the skin

Scientific Title

Research on the effects of fermentable dietary fiber and behavioral intervention on the skin

Scientific Title:Acronym

Research on the effects of fermentable dietary fiber and behavioral intervention on the skin

Region

Japan


Condition

Condition

Healthy Adults

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects on skin condition of adult women aged 20 to under 50 years old who take in foods containing fermented dietary fiber and undergo behavioral intervention (face massage and cotton packs) for 12 consecutive weeks at 6 weeks and 12 weeks.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Skin test (VISIA image analysis)

Key secondary outcomes

Skin test (stratum corneum moisture content, transepidermal water loss, skin viscoelasticity)
VAS (Visual Analog Scale) questionnaire


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Food Behavior,custom

Interventions/Control_1

Intake of foods containing fermented dietary fiber and behavioral intervention (face massage and cotton packs) for 12 weeks.

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

50 years-old >

Gender

Female

Key inclusion criteria

1. Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document
2. Japanese women who are 20 years old or more and under 50 years old
3. Persons who have concerns about their skin
4. Persons who have concerns about their gastrointestinal health

Key exclusion criteria

1. Persons who have chronic illness, receiving medication, have a serious disease history
2. Persons who are allergic to the test food (especially wheat, eggs, milk, soybeans, peaches, almonds, and oranges)
3. Persons who usually take a large amount of the test food
4. Persons who regularly do facial massages
5. Persons who regularly use face masks
6. Persons who don't regularly use lotion
7. Persons who usually take a large amount of dietary fiber
8. Persons who usually take medicine, specified health food, healthy food and supplements that may have the skin condition or other supplements that are expected to have cosmetic effects
9. Persons who regularly use vitamin A (tretinoin, retinol, retinol analogues) in their skin care
10. Persons who usually take medicine, specified health food, healthy food and supplements that may have the intestinal environment or other supplements that are expected to have cosmetic effects or foods that are expected to have prebiotic or probiotic effects
11. Persons who have experience with cosmetic treatments on the face
12. Persons with obvious inflammation on the face or skin diseases diagnosed by a doctor
13. Persons who are undergoing hormone replacement therapy
14. Persons who have eyelash extensions
15. Persons who have artificial makeup on the outer corner of the eyes
16. Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam
17. Persons who were judged as inappropriate for study participants by the principal investigator
18. Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding
19. Persons who regularly engage in aerobic exercise such as walking, jogging, or cycling (at least three times a week).

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Takamasa
Middle name
Last name Masuda

Organization

Healthcare Systems Co., Ltd.

Division name

Clinical Research Department

Zip code

105-0004

Address

Park Place Bld. 5F, 5-27-1, Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

0368092722

Email

masudat@hc-sys.jp


Public contact

Name of contact person

1st name Takamasa
Middle name
Last name Masuda

Organization

Healthcare Systems Co., Ltd.

Division name

Clinical Research Department

Zip code

105-0004

Address

Park Place Bld. 5F, 5-27-1, Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

0368092722

Homepage URL


Email

masudat@hc-sys.jp


Sponsor or person

Institute

Healthcare Systems Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Mizkan Corporation

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

The Ethics Committee of Healthcare Systems Co., Ltd.

Address

1-14-18, Shirakane, Showa-ku, Nagoya, Aichi, JAPAN

Tel

03-6809-2722

Email

soumu@hc-sys.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 09 Month 05 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

2025 Year 09 Month 05 Day

Date of IRB

2025 Year 09 Month 05 Day

Anticipated trial start date

2025 Year 09 Month 05 Day

Last follow-up date

2025 Year 12 Month 13 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 09 Month 05 Day

Last modified on

2025 Year 09 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000067483