Healthy subjects
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Aged 40-64 years. 2) BMI not less than 25.0 kg/m2, under 30.0 kg/m2 3) FPG not less than 100 mg/dL, under 126 mg/dL and/or HbA1c not less than 5.7%, under 6.5% 4) Capable of giving informed consent
Exclusion criteria
Exclusion criteria: 1) Subjects who are treated for diabetes. 2) Subjects who are received pharmacotherapy for dyslipidemia. 3) Subjects who are taking medications that affect weight fluctuation and glucose metabolism such as antidepressant. 4) Subjects who are habitually taking supplement (including "food for specified health use", and "foods with function claims") that affect weight fluctuation and glucose metabolism. 5) Subjects who are habitually drinking olive tea. 6) Subjects who had participated in intervention study using olive tea. 7) Subjects who succeeded in losing weight greater than or equal 5% in the past year. 8) Subjects who are treated for anemia or have treatment history for anemia. 9) Subjects who are enrollment in another interventional study 10) Subjects who were recognized unsuitable for this study by the Investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in body weight and abdominal circumference from baseline to 12 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in following items from baseline to 12 weeks 1) Glucose metabolic indicator 2) Dietary habit 3) Lipid metabolic indicator 4) Hepatic and renal function indicator | — |
Countries
Japan
Contacts
University of Tsukuba, Faculty of Medicene Course of clinical research and regional innovation donated by the JA Ibaraki