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A Observational study to changing pattern of Mibyeong

A Prospective Observational study to determine the changing pattern of Mibyeong in Healthy People

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002403
Enrollment
400
Registered
2017-08-04
Start date
2016-09-29
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Kyung Hee University Oriental Medicine Hospital at Gangdong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (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

Exclusion criteria

Exclusion criteria: (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

Design outcomes

Primary

MeasureTime frame
questionnaire(pain);questionnaire(sleep);questionnaire(fatigue);questionnaire(stress);questionnaire(quality of life)

Secondary

MeasureTime frame
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)

Countries

Korea, Republic of

Contacts

Public Contacthye eun

Kyung Hee University

nahyeeun1@naver.com+82-2-440-7289

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026