A study evaluating the effect of notification of postprandial hyperglycemia and supporting counter measures on the habits of eating and exercising, and on the parameters of glucose metabolism.
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000049114
- Lead Sponsor
- Suntory Global Innovation Center Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 75
Not provided
(1)Systolic pressure <90 mmHg (2)Pregnant or lactating. (3)Who donated over 200ml blood components or whole blood within the past 4 weeks prior to the current study. (4)Male who donated over 400ml whole blood within the past 12 weeks prior to the current study. (5)Female who donated over 400ml whole blood within the past 16 weeks prior to the current study. (6)Male whose blood was collected more than 1200 mL within the last twelve months when the amount of blood sampling in the current study is added. (7)Female whose blood was collected more than 800 mL within the last twelve months when the amount of blood sampling in the current study is added. (8)Who are participating in other clinical studies, or who finished clinical study within the last 4 weeks. (9)Subjects a)with disease on heart, liver, kidney or other organs complications. b)with a previous history of disease on circulatory organs. c)who are contracting diabetes. (10)Who have possibility to be diagnosed as diabetes; whose HbA1c is equal to or more than 6.5 % or have past medical history of diabetes. (11)Who have increased the frequency of hard physical activity 1 day or more after a medical check-up conducted in 2022, or who have those constant habits 3 days or more per week. (12)Who restrict diets including carbohydrate. (13)Who must follow the specific health guidance. (14)With a previous history of feeling sick after blood sampling. (15)Who have difficulty in blood sampling from peripheral vein. (16)Who drink alcohol a lot. (17)Who have irregular eating patterns. (18)Who work irregular shifts or at midnight. (19)Whose BMI is less than 18.5 or equal to or more than 30.0 kg/m2. (20)Who are contracting alcohol hypersensitivity. (21)Who are judged as unsuitable for the study by the principal investigator for other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method HbA1c
- Secondary Outcome Measures
Name Time Method