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Study on the Effector Mechanism of

Study on the Effector Mechanism of

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064346
Enrollment
Unknown
Registered
2022-10-03
Start date
2022-10-03
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

chronic sleep deprivation

Interventions

CPSD control group:Without any intervention
CPSD with pre-electroacupuncture:pre-electroacupuncture

Sponsors

Changchun University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: (1) School students aged 18 to 35 years (with imminent voluntary sleep deprivation in the coming period) with right-handedness; (2) Regular diet, no excitatory beverages consumed 1 week before the experiment; no acupuncture treatment within 1 month; (3) No pain (including dysmenorrhea), and the women were unmarried and not in the menstrual cycle at the time of examination; (4) Absence of any sleep disorder within the last month, regular work and rest, with a daily sleep time range of 7 to 9 hours; (5) Always in good health, no history of liver and kidney dysfunction, cardiovascular and cerebrovascular diseases, endocrine and immune system diseases, no history of mental diseases, no pathological or abnormal clinical findings during physical examination, normal naked or corrected visual acuity; normal BMI (18.5-25kg/m2); (6)Patients informed consent, and voluntary treatment in this study.

Exclusion criteria

Exclusion criteria: (1) Those who have recently taken psychotropic-related drugs that may interfere with the results of this experiment. (2) Having any current or prior psychiatric or neurological disorders. (3) People with sleep disorders, serious early riser or late sleeper; (4) severe heart, liver and renal insufficiency; (5) Subjects considered unsuitable for this study by the researchers: for example, people who may be claustrophobic; fear of electroacupuncture; those who have metal implants and cannot be tested by rs-fMRI.

Design outcomes

Primary

MeasureTime frame
functional Magenetic Resonance Imaging;electroencephalogram;Pittsburgh sleep quality index;Stanford Sleepiness Scale;Montreal Cognitive Assessment;Wechsler memory scale;

Secondary

MeasureTime frame
Hamilton Anxiety Scale;Hamilton Depression Rating Scale;Brain-derived neurotrophic factor(BDNF);5-hydroxytryptamine(5-HT);Melatonin;cortisol;

Countries

China

Contacts

Public ContactWang Hongfeng

Changchun University of Chinese Medicine

ccwhf@126.com13943193886

Outcome results

None listed

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