Skip to content

A pilot study on the effect of acupuncture stimulation to electroencephalography

A pilot study on the effect of acupuncture stimulation to electroencephalography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0001870
Enrollment
40
Registered
2016-04-04
Start date
2013-08-05
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

Medical Device : A total of 20 subjects (20 males, 20 females) in their 50s will receive 12 acupuncture stimulations, at 30 minutes per stimulation, for one month and their EEGs will be measured and c
and the stimulation lines will be randomly assigned. The trial will be a single-blind test in which the subjects will be unable to distinguish between real and sham stimulation.

Sponsors

Daejeon Korean Medicine Hospital of Daejeon University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Individuals who voluntarily participate in the clinical trial and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with autoimmune diseases such as asthma; 2. Individuals with skin allergies such as atopy; 3. Individuals with accompanying conditions that can affect the head, neck, and facial electromyogram (common cold, head injury, neck and jaw pain, toothache, or eye diseases); 4. Individuals who have undergone surgery within the last year or who have a serious medical history; 5. Individuals with metal prostheses inserted into their body; 6. Individuals with current medication (oriental medicine and western medicine) or who plan to take medication during clinical trials; 7. Individuals who are judged unable to maintain a sitting position at least for one hour; 8. Individuals who are unsuitable for acupuncture stimulation 9. Individuals who are judged unable to fill out the forms related to research performance; 10. Individuals with a medical history in psychiatry or with brain-related disorders; 11. Individuals who are judged unable to participate in the experiment easily due to their biorhythms (lack of sleep; drinking within 72 hours); 12. Individuals who are judged by the investigators to be unsuitable to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
P300

Secondary

MeasureTime frame
slow alpha wave amplitude and latency

Countries

Korea, Republic of

Contacts

Public ContactKwang Ho Choi

Korea Institute of Oriental Medicine

ddoongho@kiom.re.kr+82-42-229-6726

Outcome results

None listed

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