None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) female above 19 and below 60. Who can communicate and fill in the questionnaire (2) Night shift (more than from 0:00 AM to 6:00 AM) before visiting (3) Voluntarily sign the informed consent form after explained the purpose and characteristics of the clinical trial
Exclusion criteria
Exclusion criteria: (1) taking medication within 1 months due to hypertension, heart failure, myocardial infarction, arrythmia, COPD(Chronic Obstructive Pulmonary Disease), renal failure, tumor, depression (2) who diagnosed disease that can affect to autonomic nervous system such as orthostatic hypotension, diabetic neuropathy, Acute/Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Parkinsonism (3) Who took caffeine, alcohol and smoking within 12 hours before trial (4) Who took acupuncture treatment within 1 week (5) And ohters who judged unsuitable to participate in the trial by the researcher.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HF((High Frequency)) components of Heart rate variability | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate variability (Low frequency,High Frequency,LF/HF ratio, Total Power, Standard Deviation of Normal to Normal interval, Root mean square of seccesive difference, non parametric parameter);Galvanic Skin Response (GSR);Digital Infrared Thermography Imaging;Platelet activatiion level;Quantitative sensory testing | — |
Countries
Korea, Republic of
Contacts
Kyung Hee University Oriental Medical Center