Insomnia
Conditions
Interventions
Experimental group:Conventional medication + mindfulness combined with electroencephalogram biofeedback group
Control group:Conventional medication + conventional insomnia care group
Sponsors
The Fourth Affiliated Hospital of Nanjing Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Meets the diagnostic criteria for insomnia; 2. Has no history of treatment with antipsychotic drugs, anti-insomnia drugs, or sedative-hypnotic drugs in the past 2 weeks; 3. Has given informed consent to participate in the study and has a high degree of treatment compliance; 4. Actual sleep time is less than 6 hours; 5. The score of the Pittsburgh Sleep Quality Index (PSQI) is >= 7 points.
Exclusion criteria
Exclusion criteria: 1. Those with combined neurological disorders or other internal diseases that can cause insomnia; 2. Those with severe organic diseases or physical disorders of the heart, liver, lungs, kidneys, etc.; 3. Those with a history of epilepsy or brain surgery; 4. Those who are intolerant to or have contraindications to the treatment methods of this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pittsburgh Sleep Quality Index Scale;Hamilton Anxiety Scale ;Hamilton Depression Scale;Watch sleep monitoring data; | — |
Secondary
| Measure | Time frame |
|---|---|
| Insomnia severity index;Social Disability Screening Schedule;Mindful Attention Awareness Scale;Dysfunctional Beliefs and Attitudes about Sleep Scale; | — |
Countries
China
Contacts
Public ContactYuanyuan Zhang
The Fourth Affiliated Hospital of Nanjing Medical University
Outcome results
None listed