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Observational study on the Quantitative Electroencephalography(EEG) Following Acupuncture Treatment in Patients with Insomnia

Observational study on the Quantitative Electroencephalography(EEG) and Low-resolution Electromagnetic Tomography(LORETA) Following Acupuncture Treatment in Patients with Insomnia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0001673
Enrollment
38
Registered
2015-10-22
Start date
2015-08-19
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

Wonkwang University Sanbon Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) age over 20 years below 60 years 2) who is difficult to get to sleep over 30 minutes and to maintain sleep at least 3 days a week. 3) who is scoring over 8 below 21 points of Insomnia Severity Index(ISI) 4) who consent to participate in this trial and sign an informed consent

Exclusion criteria

Exclusion criteria: 1) who has severe physical disease or unstable medical status. 2) who has neurodegenerative disease including parkinson's disease, subdural hemorrhage, normal pressure hydrocephalus, brain tumor, cerebrovascular accident, epilepsy, epileptic seizure, brain surgery, head traumatic injury or cognitive impairment. 3) who has pace maker, stimulation brain devices, ventriculo-peritoneal shunt or artificial organ. 4) who intended to suicide or homicide recently 5) who has substance abuse or dependence recently 6) who has unstable(noncompliance) psychotic disorder or bipolar disorder(manic episode) recently 7) who has experience of self-injury for the past 6 months 8) The dosage of hypnotic medicine has changed for the past 2 months. 9) who has experienced the electroconvulsive therapy for the past 6 months 10) who is fear of the acupuncture, isn't appropriate to have acupuncture treatment due to high risk of bleeding 11) who is pregnant or breast feeding 12) who participated other clinical study for the past month or participate other clinical study now. 13) who is difficult to participate this study judged by investigator.

Design outcomes

Primary

MeasureTime frame
Insomnia Severity Index(ISI)

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index(PSQI);Beck depression Index(BDI);State-Trait Anxiety Inventory;Euro-Quality of Life 5 dimensions(EQ-5D);Visual Analogue Scale of General health state;Quantative electroencephalogram;pulsimeter;Preclinic Phase(=Mibyung) Questionnaire;Constitutional Questionnaire

Countries

Korea, Republic of

Contacts

Public ContactGoeun Lee

National Rehabilitation Hospital

poupee15@naver.com+82-2-6738-5804

Outcome results

None listed

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