None listed
Conditions
Interventions
Behavioral, Dietary Supplement : The study consists of a 2-week pre-intervention period and a 2-week intervention period. All participants will visit the laboratory a total of seven times: twice durin
Sponsors
The Catholic University of Korea
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Eligible participants are adult women aged 18 years or older who have no food allergies and no active skin inflammation or dermatological conditions. Inclusion criteria also require a body mass index (BMI) of 23 or higher or a body fat percentage of 28% or higher.
Exclusion criteria
Exclusion criteria: Exclusion criteria include being male, currently pregnant, or breastfeeding. Individuals who have experienced a body weight change of ±5 kg within the past three months will also be excluded. Participants with planned travel during the study period or those currently enrolled in another clinical study will not be eligible. In addition, individuals who are taking medications prescribed by a psychiatrist, or who have scheduled medical procedures involving strong magnetic or electromagnetic radiation—such as X-rays, MRI, or CT scans—during the study period will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| changes in body composition (body weight, fat mass, muscle mass) | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in CGM metrics from a continuous glucose monitoring device, changes in waist circumference, changes in blood pressure, changes in meal timing, changes in dietary intake | — |
Countries
Korea, Republic of
Contacts
Public ContactHyunji Kim
The Catholic University of Korea
Outcome results
None listed