Effect of periosteal acupuncture at Yintang point (GV28) on cognitive function of chronic insomnia and exploration of neural mechanism

Phase 1

• Conditions: chronic insomnia

• Registration Number: ITMCTR2200006489
• Lead Sponsor: Shaanxi Traditional Chinese Medicine Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

? comply with dsm-5 diagnostic criteria for insomnia.
? 18-65 years old, including 18 and 65, regardless of gender.
? the course of disease is consistent with persistent insomnia disorder (course of disease = 3 months).
? insomnia severity index (ISI) > 7.
? right hand.
? sign informed consent.

Exclusion Criteria

? insomnia associated with other mental diseases (depression, anxiety, fine score, double equality), physical diseases (pain, stroke, coronary heart disease, tumor, etc.).
? complicated with severe depression and anxiety (PHQ-9 depression screening = 20; GAD-7 anxiety screening = 19).
? insomnia caused by poor sleep hygiene.
? insomnia caused by jet lag and shift work.
? people with high risk of sleep apnea (high risk if there are = 3 positive items in the stop Bang questionnaire).
? people suffering from serious or unstable, uncontrolled chronic diseases, such as hypertension, liver and kidney function damage, etc.
? dependence or abuse of alcohol, drugs and other substances.
? have a history of central nervous system diseases such as epilepsy, brain tumor, hemangioma, encephalitis, acute brain injury, etc.
? pregnant or lactating women and those who plan to become pregnant in the near future.
? there are metal foreign bodies within 30cm of the treatment site, such as artificial cochlea, built-in pulse generator, aneurysm clip, stent, etc.
? regularly take any drugs that affect the central nervous system or sleep within 2 weeks before enrollment, such as sleeping aids, antidepressants, antipsychotics, antiepileptics, etc.
? regularly received TMS, tDCS, ect, acupuncture and other treatments within 1 month before enrollment.
? severe audio-visual impairment, unable to cooperate with the investigator to complete the study.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified