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Verification of the effect of the use of the test product on stress -Randomized crossover controlled trial-

Verification of the effect of the use of the test product on stress -Randomized crossover controlled trial- - Verification of the effect of the use of the test product on stress

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000058172
Enrollment
7
Registered
2026-03-31
Start date
2025-06-13
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Have participants smell the test product for 1 minute Apply the test product to their face with their hands for 1 minute Have participants wipe with the test product for 1 minute

Sponsors

KOBAYASHI Pharmaceutical Co., Ltd.
Lead Sponsor
Otemon Gakuin Educational Foundation
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Healthy female university students aged 18 or older who suffer from acne 2) Non-smokers 3) Not receiving medical treatment for hypertension, diabetes, mental illness, sleep disorders, or serious illnesses 4) Participants who have received an explanation of the study, fully understood the contents, and provided their own informed consent

Exclusion criteria

Exclusion criteria: 1) Heavy alcohol drinkers (average alcohol intake of 60g or more per day) 2) Individuals who have undergone hormone replacement therapy or are taking oral contraceptives within the past year 3) Individuals who are using drugs that affect the secretion of cortisol (steroids, phenytoin, phenobarbital) 4) Individuals with extremely irregular eating habits, or those with irregular lifestyles such as shift workers or night shift workers 5) Individuals taking foods for specified health uses, foods with functional claims, health foods (including supplements), etc. that take into consideration their effects on the autonomic nervous system and sleep 6) Individuals with blocked noses due to hay fever or other conditions that make it difficult to distinguish between different scents 7) Individuals who are allergic to the test products 8) Individuals who prefer fragrance-free products, or those who dislike the scent of the test product. 9) Individuals who are pregnant, wish to become pregnant, or are breastfeeding. 10) Individuals with irregular menstrual cycles (average menstrual cycle of 24 days or less, or 39 days or more). 11) Individuals who are regularly visiting a clinic for acne treatment. 12) Individuals with atopic skin. 13) Individuals who have previously experienced abnormal skin reactions such as redness, swelling, itching, irritation, discoloration (e.g., vitiligo), or hyperpigmentation after using cosmetic products containing ethanol, isopropylmethylphenol, or dipotassium glycyrrhizate.

Design outcomes

Primary

MeasureTime frame
Changes in salivary stress markers/indicators due to the use of the test product.

Secondary

MeasureTime frame
Changes in psychological stress induced by the test product. Changes in heart rate and brain waves due to the use of the test product. Questionnaire regarding skin condition and stress level prior to measurement.

Countries

Japan

Contacts

Public ContactShuu Imai

KOBAYASHI Pharmaceutical Co., Ltd. Life Science Research Department R&D Headquarters

sh.imai@kobayashi.co.jp072-640-0121

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026