Mental Fatigue
Conditions
Interventions
Experimental group:finger well-point exercise
Control group:close eyes and rest
Sponsors
Experimental Acupuncture Research Center, Tianjin University of Traditional Chinese Medicine; Tianjin Jinghai District Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: 1. Gender is not limited, aged 18-30 years old; 2. Visual acuity or corrected visual acuity above 1.0, right-handed; 3. One week before the test, maintain a regular sleep routine (about 8 hours of sleep per night), and keep a sleep diary one week before the test; 4. Pittsburgh Sleep Quality Index (PSQI) score below 5; 5. The individual has no history of mental abnormalities and family mental illness, and no negative emotions such as depression and anxiety in the near future; 6. Did not take any drugs for three weeks before the test; 7. Prohibit the intake of caffeine, tobacco, alcohol or tea, or any other substances that may affect the test results one week before the test and throughout the test; 8. Wear fNIRS without any discomfort (can withstand fNIRS monitoring for more than 30min); 9. After explaining the specific implementation steps of the test to the subjects in detail, the individual voluntarily signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Female pregnancy and menstrual period; 2. Accompanied by psychological, psychiatric, neurological, color blindness and other medical history or family history, drug abuse history; 3. Have a history of smoking, alcoholism, and drinking of strong tea and coffee; 4. History of cardiovascular disease, respiratory disease, nervous system disease, mental disorder or sleep disorder; 5. There are trauma, skin lesions, etc. on the body, or skin infections and ulcers in and around the parts involved in the test; 6. Those who have participated in other clinical researchers within one month before the trial or participated in other clinical researchers during the trial; 7. Those who do not sign the informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| visual analogue scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| reaction time;Accuracy rate; | — |
Countries
China
Contacts
Public ContactZhou Dan
Experimental Acupuncture Research Center, Tianjin University of Traditional Chinese Medicine; Tianjin Jinghai District Hospital
Outcome results
None listed