A Observational study to changing pattern of Mibyeong
- Conditions
- Not Applicable
- Registration Number
- KCT0002403
- Lead Sponsor
- Kyung Hee University Oriental Medicine Hospital at Gangdong
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 400
(1) men and women between the ages of 30-49 years:
(2) in fair subjective health
(3) fall in the ‘healthy’ group according to results of the Mibyeong survey
(4) meet two or fewer criteria of the metabolic syndrome screening test
(5) submitted the results of a NHIS health check-up received within the previous two years.
(6) Results of the above health check-up must meet one of the two conditions described below:
? overall health grade of ‘normal A’ or ‘normal B’
? blood pressure, blood glucose, total cholesterol, HDL, triglyceride, and LDL fall in the ‘normal A’ or ‘normal B’ range despite the presence of hypertension, diabetes, or dyslipidemia due to fair management of the condition(s) through pharmacotherapy, etc.
(7) able to participate independently in evaluation/ survey required in the present research
(8) able to participate in the long-term monitoring as subjects of the present research
(1) Individuals medically diagnosed with the following condition(s): cardiovascular diseases (myocardial infarction, congestive heart failure, angina, arrhythmia, etc.), cerebrovascular diseases (apoplexy, strokes, etc.), malignant tumors(cancers), psychiatric disorders (depression, anxiety disorders, etc.), arthritis(degenerative, rheumatoid), thyroid disorders(hyperthyroidism, hypothyroidism)
(2) Individuals who were on medications or received other types of treatment for internal, neurological, or psychiatric disorders within the previous month; with the exclusion of medications used to manage hypertension, diabetes, and dyslipidemia.
(3) pregnant or breastfeeding women, and women planning on becoming pregnant within the next 6 months.
(4) other individuals deemed ill-suited for participation in the present research by the principal researcher
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method questionnaire(pain);questionnaire(sleep);questionnaire(fatigue);questionnaire(stress);questionnaire(quality of life)
- Secondary Outcome Measures
Name Time Method machine measurement(vital signs);machine measurement(body composition);machine measurement(pulse wave);machine measurement(heart wave variability);questionnaire(chills and fever);questionnaire(weakness and firmness)