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The efficacy and safety of Gong's brain acupuncture therapy compared to digital cognitive-behavioral therapy in chronic insomnia

The efficacy and safety of Gong's brain acupuncture therapy compared to digital cognitive-behavioral therapy in chronic insomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086619
Enrollment
Unknown
Registered
2024-07-08
Start date
2024-07-10
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

chronic insomnia

Interventions

Gong's Brain Acupuncture Treatment Group:Group G was treated with Gong's brain acupuncture. As shown in the picture, the patient takes a sitting position, hands folded on the treatment bed, head bent
dCBT-I Group:The control group (dCBT-I group) received digital cognitive-behavioral therapy. The system was jointly developed by Maidong Shukang and Peking University Sixth Institute. It is a digital

Sponsors

Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Age range from 18 to 80 years old (including 18 and 80 years old), regardless of gender; ? Meets the diagnostic criteria for non organic insomnia in the Diagnostic and Statistical Manual of Mental Disorders, Version V (DSM-V) of the United States, with a course of more than 3 months; include (a) The chief complaint is either difficulty falling asleep, difficulty maintaining sleep, or poor sleep quality; (b) This sleep disorder occurs at least three times a week and lasts for more than a month; (c) Focusing day and night on insomnia, overly concerned about the consequences of insomnia; (d) The dissatisfaction with the amount and/or quality of sleep has caused significant distress or affected social and occupational functions. ? No serious life or psychological events that interfere with sleep within three months (excluding fear of sleep); ? Voluntarily participate in the study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: ? Insomnia caused by sleep apnea syndrome, restless leg syndrome, pain, etc; ? Those who are using any other insomnia treatment method and are unable to stop the treatment method; ? Individuals with severe psychological stress that has not been cured or is currently undergoing treatment; ? Individuals with severe physical illnesses; ? Concomitant severe mental illness (such as severe anxiety, depression, schizophrenia, etc.); ? Alcohol and other dependent individuals; ? Travelers who work in shifts or night shifts and frequently cross time zones; ? Other situations that the researcher deems unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Insomnia Severity Index;Sleep Quality;

Secondary

MeasureTime frame
Depression level;Sleep efficiency/ duration;Anxiety level;Quality of life;Fatigue level;

Countries

China

Contacts

Public ContactZongwang Zhang

Liaocheng People's Hospital

zongwangzhang@sdu.edu.cn+86 133 4625 6809

Outcome results

None listed

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