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Study on the effect and mechanism of Electroacupuncture of ''Adjust Zang-fu and Arouse Spirit'' on the brain cognitive function of chronic partial sleep deprivation

Study on the effect and mechanism of Electroacupuncture of ''Adjust Zang-fu and Arouse Spirit'' on the brain cognitive function of chronic partial sleep deprivation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200061792
Enrollment
Unknown
Registered
2022-07-02
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

the brain cognitive function of chronic partial sleep deprivation

Interventions

Chronic partial sleep deprivation with electroacupuncture group:'Adjust Zang-fu and Arouse Spirit' electroacupuncture

Sponsors

Changchun University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for chronic partial sleep deprivation group (1) All medical workers (21-50 years old) on long-term regular night shift, right-handed; (2) The duration of intermittent SD was more than 6 days,and sleep was less than 5h per day; (3) sleep disorder,PSQi > 7;Montreal Cognitive Assessment Scale (MoCA) = 26; (4) Have always been in good health, have no history of liver and kidney dysfunction, cardiovascular and cerebrovascular diseases, endocrine and immune system diseases, and have no history of mental diseases, and have no pathological or abnormal clinical findings during physical examination; (5) Fixed job content, college degree or above, fixed activity city.

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. people who are sensitive to acupuncture and have acupuncture sickness; 2. Sleep time > 5h during night shift; 3. a history of smoking, drinking alcohol, drinking espresso, and a history of sleep disorders; 4. Suffer from physical or mental diseases that affect sleep, such as depression and apnea syndrome; 5. participants in other clinical studies or received acupuncture treatment within 7 days prior to enrollment; 6. Ingestion of prescription or non-prescription drugs within 7 days before treatment; 7. Leave the place of daily activities during the study period; 8. Refuse to participate in the survey or interrupt the survey due to poor cooperation; 9. Patients implanted with metal implants, such as pacemakers, defibrillators, cardiac stents, artificial heart valves, metal clips after aneurysm surgery, drug perfusion devices, nerve stimulators, bone growth stimulators and any other type of biological stimulators, metal sutures, etc.; Patients with bullets, broken shrapnel or iron sand particles in the body, or with fixed steel plates, nails and screws after fracture; Patients with internal artificial limbs or joints, penile prostheses, hearing AIDS, cochlear implants, middle ear implants, metallic foreign bodies in the eye, implants in the head and face, etc. 10. Patients with claustrophobia.

Design outcomes

Primary

MeasureTime frame
functional Magenetic Resonance Imaging;Magnetic resonance spectrum(MRS);Montreal Cognitive Assessment (MoCA);Pittsburgh sleep Index;

Secondary

MeasureTime frame
Stanford Sleepiness Scale(SSS);Wexler Memory Scale (WMS);Hamilton Anxiety Scale (HAMA);Hamilton Depression Scale (HAMD);Interleukin-6;Interleukin-1 ß;

Countries

China

Contacts

Public ContactHongfeng Wang
ccwhf@126.com+86 13943193886

Outcome results

None listed

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