None listed
Conditions
Sponsors
Ewha Womans University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Subject who voluntarily agree to participate and signs informed consent form 2) Aged more than 19 years and less less than 65 years, women and men 3) Those who have a body mass index (BMI) of 25kg/ bb m*2 or more and less than 30kg/m*2 4) Those who can follow the diet and exercise guidelines during the intervention period
Exclusion criteria
Exclusion criteria: 1) Those who have taken or are likely to take medications that affect body weight, blood sugar, lipids, or intestinal health within one month of the first visit 2) Those who have taken antibiotics within 2 months of the first visit or are likely to take it during the study 3) If you have, 1.Uncontrolled hypertension 2. Those who have been diagnosed with diabetes or are determined to need treatment, or who have fasting blood sugar level of 180 mg / dL or more 3. Liver dysfunction or hepatobiliary disease 4. Renal dysfunction 5. Hyperthyroidism and hypofunction, Cushing's syndrome 6. If you have a medical history of severe central nervous system disorders that require hospitalization or medication 7. Those with severe cerebrovascular disease, heart disease. However, dizziness If there is no medical history, it may be excluded at the discretion of the researcher. 8. Malignant tumor, lung disease, musculoskeletal disease, immune system or inflammatory disease 9. A person who complains of gastrointestinal disorders or severe gastrointestinal symptoms such as heartburn, indigestion or severe constipation 10) Those who have continuously consumed dietary supplements or herbal medicines affecting their weight, blood sugar, and lipids within one month of their first visit. 11) Those who have consistently consumed foods,Probiotics 12) Those who have hypersensitivity to the test / control food or ingredients or have experienced severe food allergic reactions. 13) Participants in other human application research within 1 month of first visit 14) Pregnant or lactating women 15) Those who have difficulty using a smartphone or computer 16) If the researcher deems inappropriate to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body fat improvement indicator | — |
Secondary
| Measure | Time frame |
|---|---|
| Body fat related metabolic indicators | — |
Countries
Korea, Republic of
Contacts
Public ContactKyuyoung Han
Ewha Womans University
Outcome results
None listed