Clinical Trials in China / NCT07340268
Recruiting
Not applicable
The Effects of Transcranial Current Stimulation on Insomnia
NCT07340268 · tracked via the Priya Life Science China tracker
Condition(s) studied
Insomnia, Psychophysiological
Investigational drug(s) / intervention(s)
transcranial current stimulationSham stimulation
transcranial current stimulation: consecutive daily 20-min, 1.1-mA sessions
Sham stimulation: only wore the device and had no stimulation
Study summary
Effect of transcranial current stimulation on insomnia disorder
Eligibility
Inclusion Criteria:
* Clinical diagnosis of insomnia disorder
* Cooperate to complete the questionnaire surveys
Exclusion Criteria:
* Presence of mental disorders
* Current use of central nervous system stimulants
* Use of analgesics,sedatives or hypnotic medications, theophylline preparations, steroid medications
* Alcohol abuse or regular alcohol consumption
* Diagnosis of other sleep disorders, including obstructive sleep apnea, rapid eye movement sleep behavior disorder, or restless legs syndrome
* Sleep disorders secondary to organic diseases, such as epilepsy, diabetes, or renal failure
* Shift work or irregular work schedules that disrupt normal circadian rhythms
* Use of medications affecting central nervous system function within the past one month
* Recent sleep-related confounding behaviors within the past two weeks, including staying up late, alcohol consumption, or smoking
* Presence of organic brain lesions on head MRI and contraindications to MRI examination
Primary outcome measure(s)
- Change in global blood-oxygen-level-dependent (gBOLD) signal amplitude — 2 weeks and 3 months
The amplitude of the global blood-oxygen-level-dependent (gBOLD) signal was derived from resting-state functional MRI and reflects the overall magnitude of spontaneous brain activity. Unit of Measure: Z-score - Change in resting-state functional connectivity strength — 2 weeks and 3 months
Resting-state functional connectivity strength was calculated as the correlation coefficient between predefined brain regions based on functional magnetic resonance imaging data. - Change in amplitude of low-frequency fluctuations — 2 weeks and 3 months
Amplitude of low-frequency fluctuations was calculated from resting-state fMRI to quantify spontaneous neural activity. - Change in regional homogeneity — 2 weeks and 3 months
Regional homogeneity was used to assess the synchronization of local spontaneous brain activity - Change in phase difference of dynamic cerebral autoregulation — 2 weeks and 3 months
Dynamic cerebral autoregulation was assessed using the phase difference between cerebral blood flow velocity and arterial blood pressure fluctuations. Larger phase differences indicate better autoregulatory function. - Change in gain of dynamic cerebral autoregulation — 2 weeks and 3 months
Gain represents the magnitude of cerebral blood flow velocity changes in response to blood pressure fluctuations, with lower gain values indicating more effective autoregulation.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| the First Hospital of Jilin University | Ch’ang-ch’un | Jilin | Completed |
| the First Hospital of Jilin University | Ch’ang-ch’un | Jilin | Recruiting |
More Zan Wang trials in China
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07340268 on ClinicalTrials.gov ↗ ← All trials in China