Intermittent Theta Burst for the Treatment of Alcohol Use Disorders in Veterans

Stanford University

Status: Terminated

Conditions: Cigarette Smoking; Depressive Disorder; Alcohol Use Disorder

Treatments: Device: Intermittent theta burst transcranial magnetic stimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT03291431

41896

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy of intermittent theta burst repetitive transcranial magnetic stimulation (iTBS) as a treatment for Veterans with an alcohol use disorder (AUD) to decrease the exceedingly high rate of relapse associated with this condition. iTBS has demonstrated equivalent efficacy and safety to repetitive transcranial magnetic stimulation employing 10Hz stimulation protocols in treatment of depressive disorders. The advantage of iTBS is that it can be delivered in approximately 5 minutes where conventional 10Hz repetitive transcranial magnetic stimulation (rTMS) protocols are typically 20-25 minutes. It is hypothesized that Veterans with AUD who receive active iTBS applied to the left dorsolateral prefrontal cortex (DLPFC), compared to controls (i.e., Veterans with AUD who receive sham iTBS), will show significant decreases alcohol craving, depressive symptomatology and cigarette consumptions, as well as improved neurocognition, a longer period of abstinence, and a lower overall rate of relapse over 6 months following standard psychosocial treatment for AUD at VA substance treatment clinics. In exploratory analyses, it is also predicted that magnetic resonance measures of left DLPFC glutamate concentration, volume of anterior frontal cortical brain regions, and performance on fMRI tasks interrogating the function of the salience/reward circuits will serve as biomarkers of iTBS treatment response. The goal of this proposal is to implement treatment that effectively promotes sustained abstinence in Veterans with AUD, given long-term abstinence is related to optimal neurobiological, neuropsychological and psychosocial recovery and functioning.

Enrollment: 17 patients

Sex: All

Ages: 21 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 21-65 years of age
• Meet Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) criteria for alcohol use disorder, and alcohol is self-identified as primary substance of misuse.
• Actively in treatment at VA Palo Alto HCS Addiction Treatment Service
• Able to read, verbalize understanding, and voluntarily sign the Informed Consent Form prior to participation in study procedures.

Exclusion criteria

• History of Schizophrenia Spectrum Disorders, Bipolar Disorders, a
• Current substance use disorder that exceeds the severity of the AUD (based on DSM-5 diagnostic criteria)
• Current use of an FDA approved medication (i.e., disulfiram, acamprosate, and naltrexone) for treatment of AUD,
• Active current suicidal intent or plan (patients with a previous clinical flag for risk for suicide will be required to have an established safety plan involving their primary psychiatrist and the treatment team before entering the clinical trial),
• Any form of previous TMS or electroconvulsive treatment.
• Thyroid disease,
• Unstable congestive heart failure, angina, other severe cardiac illness as defined by treatment regimen changes in the prior 3 months
• Cerebrovascular accident
• Cancer if < 1 year since end of treatment
• Unstable diabetes
• COPD requiring oxygen supplementation
• Alzheimer's disease
• Parkinson's disease
• Any Biomedical implants with ferromagnetic content
• Neurostimulation devices, cardiac pacemakers or any magnetic resonance contraindications
• Traumatic brain injury with self-reported or observed loss of consciousness > 30 minutes
• Any primary or traumatically induced seizure disorder
• Lack of fluency in English, Wechsler Adult Reading Test below the 7th percentile (i.e., moderate or greater impairment in estimated general intelligence),
• Females who are pregnant or actively attempting pregnancy (conservative exclusion for magnetic resonance research),
• Current use of any medication or substance that is documented to lower seizure threshold or has been identified as a contraindication for TMS treatment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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17 participants in 2 patient groups

Active iTBS

Active Comparator group

Description:

Participants will be randomized to active or sham iTBS.

Treatment:

Device: Intermittent theta burst transcranial magnetic stimulation

Sham iTBS

Sham Comparator group

Description:

Participants will be randomized to active or sham iTBS.

Treatment:

Device: Intermittent theta burst transcranial magnetic stimulation