Amphetamine Use Disorders Clinical Trial
Official title:
Closed-loop Neuromodulation Based on Individualised EEG Biomarkers of Methamphetamine Use Disorder
NCT number | NCT06457243 |
Other study ID # | MZhao-019 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2024 |
Est. completion date | August 2025 |
Using specific EEG biomarkers in methamphetamine-dependent individuals, this study systematically probes closed-loop continuous Theta-burst Stimulation (cTBS) based on brain states, assessing dosage, neurologic and behavioral effects, while comparing its efficacy with traditional open-loop cTBS methods.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | August 2025 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Individuals aged between 18 and 60 years, irrespective of gender, having completed a minimum of 9 years of education and capable of effectively cooperating in questionnaire evaluations. - Meet the diagnostic criteria set forth by the DSM-V concerning the amphetamine-type substance addiction. - A history of utilizing amphetamine-type substances for a duration not less than one year, with a frequency of use being at least once per week. - Consent to actively cooperate in the completion of subsequent follow-up assessments. Exclusion Criteria: - Severe cognitive functional impairments manifested through a history of head trauma, cerebrovascular diseases, epilepsy, etc., or usage of cognitive enhancement drugs in the past 6 months; an intellectual disability with an IQ score less than 70. - A diagnosis of schizophrenia or other severe mental illnesses as per the DSM-5 criteria. - Abuse or dependence on other psychoactive substances (excluding nicotine) within the past 5 years. - Severe organic diseases that might compromise study participation. - Contraindications to cTBS, such as a history of epileptic seizures or the presence of metallic implants in proximity to the head. |
Country | Name | City | State |
---|---|---|---|
China | Min Zhao, PhD | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai Mental Health Center |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of Craving assessed by Visual Analog Scale (VAS) | The intensity of psychological craving in MA dependents was assessed using the Visual Analogue Scale (VAS), where individuals rated their cravings on a scale from 0 to 10, with higher scores indicating greater levels of craving. The VAS scores were utilized based on two conditions: during a resting state and when subjected to cue induction involving images associated with methamphetamine, serving as the criteria for evaluation.
individuals rated their cravings on a scale from 0 to 10, with higher scores indicating greater levels of craving. The VAS scores were utilized based on two conditions: during a resting state and when subjected to cue induction involving images associated with methamphetamine, serving as the criteria for evaluation. |
through study completion, an average of 1 month | |
Secondary | Changes of electroencephalogram power spectrum | Resting-state EEG can be used to extract power spectra and electrode functional connectivity; on-task EEG can be used to isolate time-frequency features during non-stimulated trials to extract alpha, beta, theta, and gamma band energy of the parietal and occipital electrodes. Both can be used to assess changes in neural activity before, during, and after their restimulation. | through study completion, an average of 1 month | |
Secondary | Probabilistic inversion learning task | The matching of symbols and colours was reversed without informing the subjects and their cognitive flexibility in the reversed condition was assessed | through study completion, an average of 1 month | |
Secondary | Anxiety | The reduction rate in the Beck Anxiety Inventory (BAI) scores was calculated before and after intervention to assess the rate of decrease in anxiety levels among MA dependents. | through study completion, an average of 1 month | |
Secondary | Depression | The reduction rate in the Beck Depression Inventory (BDI) scores was calculated before and after the intervention to evaluate the rate of reduction in their levels of depression. | through study completion, an average of 1 month | |
Secondary | sleep quality | Improvement in subjects' sleep before and after the intervention as assessed by the Pittsburgh Sleep Quality Index scale (PSQI) | through study completion, an average of 1 month |
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