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
- Conditions
- Not Applicable
- Registration Number
- KCT0002218
- Lead Sponsor
- Wonkwang University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
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.
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.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Southampton Acupuncture questionnaire
- Secondary Outcome Measures
Name Time Method Acupuncture Perception Questionnaire(APQ);Acupuncture Deqi Questionnaire(ADQ);The CARE measure;Quantative electroencephalogram