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Research on how rapport accomplished through 'Drawing the room of mind' influences QEEG changes and sensation of accupuncture on the Shenmen(HT7) accupoint: through randomized control trial on healthy subjects in a single center

Research on correlation between rapport accomplishment and the subjects' accupuncture sensation and QEEG changes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002218
Enrollment
40
Registered
2017-02-08
Start date
2016-10-21
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 : This clinical research is conducted with subjects who voluntarliy submited to a consent and were reviewed according to the inclusion or exclusion criteria of the clinical trial plan.

Sponsors

Wonkwang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) age over 20 years below 49 years 2) Does not indulge in smoking, tea or coffee, has regular diet and a normal sleeping pattern. 3) right-handed. 4) Were informed of the purpose and process of this clinical trial and voluntarliy consented to it.

Exclusion criteria

Exclusion criteria: 1) Who received accupuncture at least once, since 3 months before the clinical trial 2) Who has a severe physical illness or medically unstable (Decided by the clinical trial conducter or medical expert. 3) Who has a congenital illness, psychological illness , central nervous problem , peripheral nervous probelm, endocrinal illness, immunodisease, heart probelm, liver problem, renal illness. 4) Who has a neurological illness such as head trauma or psychological history such as major depressive disorder, anxiety disorder, bipolar disorder, schizophrenia. 5) Who has pace maker, stimulation brain devices, ventriculo-peritoneal shunt or artificial organ. 6) Who took medicine other then vitamin since one week before the clinal trial.(example: beta blocker, aspirin, Non-steroidal anti-inflammatory drugs(NSAIDs), steroids, phobithiazines, Selective Serotonin Reuptake Inhibitors(SSRI), statins, angiotensin converting enzyme (ACE) inhibitors ,etc) 7)Who took caffeine contained products since at least 2 hours before the clinal trial.(example: Coffee, coffee milk, Blank tea, Green tea, cocoa, coke, chocolate, caffeine contained energy drinks. 8) Who fears of the acupuncture, or isn't appropriate to have acupuncture treatment due to high risk of bleeding 9) Who is pregnant or breast feeding 10)Who participated in other clinical study for the past month or is participating in other clinical studies currently. 11) Who is difficult to participate in this study judged by investigator.

Design outcomes

Primary

MeasureTime frame
Southampton Acupuncture questionnaire

Secondary

MeasureTime frame
Acupuncture Perception Questionnaire(APQ);Acupuncture Deqi Questionnaire(ADQ);The CARE measure;Quantative electroencephalogram

Countries

Korea, Republic of

Contacts

Public ContactGoeun Lee

National Rehabilitation Hospital

poupee15@naver.com+82-31-390-2762

Outcome results

None listed

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