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A study on the relationship between electroencephalography and meridians in healthy subjects

A study on the relationship between electroencephalography and meridians in healthy subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008928
Enrollment
200
Registered
2023-11-06
Start date
2023-10-23
Completion date
Unknown
Last updated
2023-11-13

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 Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult men and women between the ages of 19 and 75 2. Those who have confirmed that there are no functional/organic diseases or clinically significant findings through medical history and physical examination 3. Participants or their legal representatives have voluntarily given written consent to participate in the study

Exclusion criteria

Exclusion criteria: 1) Participants or their legal representatives are unable to understand the consent form, or are unable to understand the main contents of the study, making it difficult for them to participate in the study. 2) Those with a history of neurological disease (traumatic brain injury, epilepsy, dementia, etc.) or childhood neurological disease 3) Those with a history of psychiatric disease 4) Those with systemic diseases that may affect the central nervous system (e.g. endocrine or metabolic diseases) 5) Those with alcohol and drug abuse or dependence 6) Those with serious behavioral and conduct disorders 7) Those who have experienced problems with academic and social activities 8) Those who take drugs that may affect the central nervous system 9) Those with clinically significant results in cognitive function on CNT 10) Those who are in high risk group for one or more of the state anxiety and trait anxiety in BDI, STAI-KYZ, or those who are in moderate risk group for two or more of the tests. 11) Those whom the clinical trial manager or clinical trial investigator determines to be difficult to conduct clinical research due to other reasons

Design outcomes

Primary

MeasureTime frame
Electroencephalogram data

Secondary

MeasureTime frame
1) Questionnaire of Cold-Heat Pattern Identification 2) Deficiency and Excess Pattern Identification Questionnaire

Countries

Korea, Republic of

Contacts

Public ContactYunna Kim

Kyung Hee University Oriental Medical Center

yunna.anna.kim@gmail.com+82-2-958-9188

Outcome results

None listed

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