Sleep Disorder
Conditions
Keywords
Sleep quality and skin conditions
Brief summary
The main objective of the study is to observe changes in the subjects' sleep quality, skin condition and life status after 4 weeks of using a sleep aid drink (AOXMED Poria γ-aminobutyric acid drink). This is a single-center, randomized, double-blind, controlled, 4-week (28-day) clinical study conducted in Chinese healthy women aged 25-55 years old who were offered a sleep aid drink.
Detailed description
The study population is 70 healthy Chinese women aged 25-55 years with a PSQI ≥ 7 (presence of sleep disorder) who report current problems with dryness, roughness, dullness and lack of elasticity on their face. The subjects will be randomly divided into an experimental group and a control product group of 35 subjects each, and the distribution of age and total hours of sleep will be more or less equal in both groups. Subjects will be formally enrolled after on-site assessment and will undergo follow-up site visits and test product administration. During the test cycle, subjects in the experimental group will take a drink with the active ingredients of Poria, Poria and GABA, and subjects in the control product group will take a control drink without Poria, Date Palm and GABA ingredients for 4 weeks. To avoid the influence of different skincare products on the results, all subjects will be asked to use the basic skincare products with only moisturizing ingredients provided by the sponsor during the test period. The efficacy of the test products will be verified by comparing the changes in sleep quality, skin condition and life status of the subjects before and after taking the test products for 2 and 4 weeks, and by comparing the differences in sleep quality, skin condition and life status between the test and control groups.
Interventions
COMBINATION_PRODUCTDrinks with active ingredients such as poria and GABA
Take drinks half an hour before bedtime, 10ml/bag/day, daily. Subjects are uniformly using skin care products provided by the sponsor during the test.
Sponsors
Botanee Group Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
FEMALE
Age
25 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
1. 25-55 years old, Chinese female; 2. PSQI index ≥ 7 (presence of sleep disorders); 3. The subject's self-reported facial problems such as dryness, roughness, dullness, and lack of elasticity; 4. The BMI of the subjects was between 18\ 24kg/m2; 5. After the doctor's clinical evaluation, there are mild facial skin roughness (1 point and above) and mild to moderate overall facial wrinkles (3\ 6 points); 6. Corneometer base measurement of facial skin moisture in 15\ 45 (Corneometer Unit, C.U.) Between; 7. Have basic Chinese reading ability; 8. can use smartphones; 9. Be in good health and free of any other chronic diseases other than skin problems and sleep disorders or diseases being treated; 10. Voluntarily participate in the test and sign the informed consent form; 11） Willingness to comply with all evaluation requirements;
Exclusion criteria
1. Products with anti-wrinkle, firming, repairing and nourishing effects are not included in the skin care products used; 2. Intend to become pregnant, or are pregnant or breastfeeding; 3. Have a history of alcoholism; 4. Have a history of allergies; 5. Participated in any clinical trial evaluation within 1 month; 6. Those who have applied any anti-inflammatory drugs to the test site within the past two months; 7. Those who have suffered from skin diseases (such as psoriasis, eczema, psoriasis, skin cancer, etc.); 8. patients with insulin-dependent diabetes; 9. Patients with asthma or other chronic respiratory diseases who are being treated; 10. Have taken/injected anti-allergic drugs in the past 1 month; 11. Patients who have received anti-cancer chemotherapy or immunotherapy patients within the past 6 months; 12. Have any other health problems or chronic diseases; 13. Applying retinoids, A hydroxy acids, salicylic acids, hydroquinone within the past 3 months, or prescription drugs (antibiotics, retinoids, A hydroxy acids and steroids) in use within the past 6 months, oral contraceptives (if you have been taking the same contraceptive pills for the past 6 months, you can continue to take them); 14. Experts or professionals believe that there are other iatrogenic reasons that will affect the evaluation results; 15) Those who have undergone surgery, plastic surgery or organ transplantation in the past year.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the Pittsburgh Sleep Quality Index | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline PSQI index at 2 weeks by questionnaire. Obtain change from Baseline PSQI index at 4 weeks by questionnaire. |
| Changes in the sleep duration | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline sleep duration at 2 weeks by sleep quality monitoring bracelet. Obtain change from Baseline sleep duration at 4 weeks by sleep quality monitoring bracelet. |
| Sleep Quality Assessment after 2-week application | Week2 | Obtain data on agreement with sleep improvement by sleep quality self-assessment questionnaire |
| Sleep Quality Assessment after 4-week application | Week4 | Obtain data on agreement with sleep improvement by sleep quality self-assessment questionnaire |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the individual type angle | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline Individual type angle at 2 weeks by Colorimeter. Obtain change from Baseline Individual type angle at 4 weeks by Colorimeter. |
| Changes in the proportion of crow's feet area | Week0（Baseline）、Week2、Week4 | Calculate the proportion of crow's feet area by Visia CR images. Obtain change from Baseline proportion of crow's feet area at 2 weeks. Obtain change from Baseline proportion of crow's feet area at 4 weeks. |
| Changes in the proportion of fine lines under the eye | Week0（Baseline）、Week2、Week4 | Calculate the proportion of fine lines under the eye by Visia CR images. Obtain change from Baseline proportion of fine lines under the eye at 2 weeks. Obtain change from Baseline proportion of fine lines under the eye at 4 weeks. |
| Changes in the degree of wrinkle severity | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline degree of wrinkle severity at 2 weeks by Dermatologist evaluation according to Skin Aging ATLAS of Asian Type. Obtain change from Baseline degree of wrinkle severity at 4 weeks by Dermatologist evaluation according to Skin Aging ATLAS of Asian Type. |
| Changes in the skin hydration | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline skin hydration at 2 weeks by Corneometer. Obtain change from Baseline skin hydration at 4 weeks by Corneometer. |
| Changes in the CIE RGB of skin tone | Week0（Baseline）、Week2、Week4 | Dermatologist use PANTONE SkinTone (Pantone color card) skin color guide to evaluate skin tone grade of subjects. Find the CIE RGB corresponding to the skin tone grade in Pantone ColorManager software and convert it into a color value using the formula for data analysis: CIE RGB = R+G\*256+B\*256\*256. Calculate the change from Baseline CIE RGB of skin tone at 2 weeks. Calculate the change from Baseline CIE RGB of skin tone at 4 weeks. |
| Skin condition Assessment after 2-week application | Week2 | Obtain data on agreement with skin condition improvement by skin condition self-assessment questionnaire |
| Skin condition Assessment after 4-week application | Week4 | Obtain data on agreement with skin condition improvement by skin condition self-assessment questionnaire |
| Changes in the satisfaction with the quality of life | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline satisfaction with the quality of life at 2 weeks accessed by WHOQOL-100 questionnaire. Obtain change from Baseline satisfaction with the quality of life at 4 weeks accessed by WHOQOL-100 questionnaire. |
| Changes in the grade of skin dryness | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline grade of skin dryness at 2 weeks by Dermatologist evaluation according to 5-point dryness scale. Obtain change from Baseline grade of skin dryness at 4 weeks by Dermatologist evaluation according to 5-point dryness scale. |
| Changes in the skin glossiness | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline skin glossiness at 2 weeks by Glossymeter. Obtain change from Baseline skin glossiness at 4 weeks by Glossymeter. |
| Changes in the skin firmness | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline skin firmness at 2 weeks by cutometer. Obtain change from Baseline skin firmness at 4 weeks by cutometer. |
| Changes in the skin elasticity | Week0（Baseline）、Week2、Week4 | Obtain change from Baseline skin elasticity at 2 weeks by cutometer. Obtain change from Baseline skin elasticity at 4 weeks by cutometer. |
Countries
China
Outcome results
None listed