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Novel Intervention for Amphetamine-type Stimulants Addiction

The Repetitive Transcranial Magnetic Stimulation (rTMS) for Amphetamine-type Stimulants Addiction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02713815
Enrollment
60
Registered
2016-03-21
Start date
2016-07-31
Completion date
2019-07-31
Last updated
2019-12-03

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

Conditions

Amphetamine Addiction

Keywords

Amphetamine-type stimulants, prefrontal-striatal circuits, rTMS, Glutamate/GABA, motivational and cognitive intervention

Brief summary

The repetitive transcranial magnetic stimulation (rTMS) will be used to treat amphetamine-type stimulant (ATS) addiction.

Detailed description

The Glutamate and GABA deficits in prefrontal cortex play a vital role in ATS addiction and relapse, and proposed repetitive transcranial magnetic stimulation (rTMS) as a novel interventions. Focused on evaluating Glutamate/GABA functions in prefrontal cortex and functional connectivity with deep brain regions, neuropsychological tests, biochemical tests, magnetic resonance spectroscopy (MRS) and functional MRI will be used to investigate the neurobiological mechanism of ATS addiction and relapse. These methods will also be used to evaluate the efficacy of the novel intervention and investigate the mechanisms. The study will be very helpful to develop novel interventions in clinical practice and decrease ATS-related harm for both the patients and their families.

Interventions

RADIATIONrepetitive transcranial magnetic stimulation (rTMS)

Stimulate the dorsomedial prefrontal cortex for 4 weeks by Theta-burst stimulation (TBS), once a day

Stimulate the dorsomedial prefrontal cortex for 4 weeks by sham Theta-burst stimulation (TBS), once a day

Sponsors

Yunnan Institute For Drug Abuse
CollaboratorUNKNOWN
Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* In accordance with the Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) for methamphetamine (MA) use disorders * Dextromanual

Exclusion criteria

* Have a disease that affect cognitive function such as history of head injury, cerebrovascular disease, epilepsy, etc * Have cognitive-promoting drugs in the last 6 months * Other substance abuse or dependence in recent five years (except nicotine) * Mental impairment, Intelligence Quotient (IQ) \< 70 * Mental disorders * Physical disease

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Craving for ATS assessed by Visual Analog Scales (VAS) at 1 monthBaseline and 1 monthevaluate all participants' craving for ATS by Visual Analog Scales (VAS)

Secondary

MeasureTime frameDescription
Number of participants who relapse1 monthFollow up with patients after discharge, evaluate number of participants who relapse
Depression status assessed by Patient Health Questionnaire-9(PHQ-9)1 monthevaluate all participants' depression status by Patient Health Questionnaire-9(PHQ-9)
Anxiety status assessed by Generalized Anxiety Disorder Screener (GAD-7)1 monthevaluate all participants' anxiety status by Generalized Anxiety Disorder Screener (GAD-7)
Cognitive function assessed by Cogstate Battery1 monthevaluate all participants' cognition by Cogstate Battery Chinese version
Functional connectivity assessed by MRI1 monthevaluate all participants' functional connectivity in the brain by MRI

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026