Healthy Adults
Conditions
Interventions
Consume a fermentable fiber-containing food between meals daily for 6 weeks.
Sponsors
Healthcare Systems Co., Ltd.
Eligibility
Sex/Gender
Female
Inclusion criteria
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 intestinal health
Exclusion criteria
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 usually take a large amount of dietary fiber 5.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 6.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 7.Persons who have experience with cosmetic treatments on the face 8.Persons who have inflammation or skin diseases on the face 9.Persons who are undergoing hormone replacement therapy 10.Persons who have eyelash extensions 11.Persons who have artificial makeup on the outer corner of the eyes 12.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 13.Persons who were judged as inappropriate for study participants by the principal investigator 14.Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Skin test (stratum corneum moisture content, transepidermal water loss, skin viscoelasticity, VISIA image analysis) | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS (Visual Analog Scale) questionnaire Fecal examination (intestinal microflora, fecal short-chain fatty acid concentration) | — |
Countries
Japan
Contacts
Public ContactKosei Nishikawa
Healthcare Systems Co., Ltd. Clinical Research Department
Outcome results
None listed