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Study on the Clinical effect of electroacupuncture on Acute Sleep deprivation and event-related potentials affecting the Control of brain inhibition

Study on the Clinical effect of electroacupuncture on Acute Sleep deprivation and event-related potentials affecting the Control of brain inhibition

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005562
Enrollment
Unknown
Registered
2022-01-30
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Acute sleep deprivation

Interventions

Control group:Acute sleep deprivation
Treatment group:Acute sleep deprivation

Sponsors

The Third Affiliated Hospital of Henan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 24 Years

Inclusion criteria

Inclusion criteria: (1) Male college students in good health. (2) 18-24 years old, right-handed according to the revised Edinburgh handedness questionnaire. (3) The visual acuity is normal after naked vision or correction. (4) The state of sleep awakening is normal, and there is no special sleep rule, that is, there are no people who wake up early and late, and there is no history of shift. The self-made "sleep log" table and interview show that the subjects have good sleep habits. (5) Symptom checklist 90 (symptom list-90 SCL Mel 90), the total average score is less than 1, and the score of each factor is less than 1. (6) the score of Pittsburgh Sleep quality Index (PSQI) is less than 5. (7) No habit of drinking coffee, tea, drinking or smoking. (8) voluntarily sign a written informed consent.

Exclusion criteria

Exclusion criteria: (1) In the past month, he has taken sedative and sleep-aiding drugs, such as estazolam, alprazolam, etc. (2) Have received acupuncture and moxibustion treatment in the past one month. (3) Patients with severe heart, liver, kidney, mental illness or coagulation dysfunction. (4) Family history of mental illness and history of infectious diseases. (5) People with allergies, especially those who are allergic to needles. (6) Implantation of cardiac pacemaker or implantable electronic equipment.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment;

Secondary

MeasureTime frame
False alarm rates;N2 latency;N2 amplitude;P3 latency;The Epworth Sleeping Scale;Fatigue Scale-14;Hit rates;False alarm rate time;P3 amplitude;Hit rate time;

Countries

China

Contacts

Public ContactChen Xinwang
36137207@qq.com13526652895

Outcome results

None listed

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