Phase
Condition
Stimulant Use Disorder
Treatment
Deep Transcranial Magnetic Stimulation (dTMS) H4 coil - Active
Deep Transcranial Magnetic Stimulation (dTMS) H4 coil - Sham
Clinical Study ID
Ages 25-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion:
Must be within the age range of 25-75.
Participants must meet Diagnostic and Statistical Manual of Mental Disorders, 5thEdition (DSM-5) criteria for moderate to severe MUD (≥4 diagnostic symptoms).
Participants must be able to obtain a Motor Threshold (MT), which will be determinedduring the screening process.
Participants must have an adequately stable condition and environment to enableattendance at scheduled clinic visits.
Participants must be able to read, verbalize, understand, and voluntarily sign theInformed Consent Form prior to participation in study procedures in English.
If participants are on a medication regimen for comorbid symptoms, that regimen willbe stable for the duration of the study and patient will be willing to remain onthis regimen during the treatment phase.
Participants must be fluent in English
Exclusion
Exclusion criteria:
Transcranial magnetic stimulation (TMS) and magnetic resonance imaging (MRI)contraindications: such as a cardiac pacemaker, cochlear implant, or an implanteddevice (deep brain stimulation, ferromagnetic metal in the head and body,claustrophobia, pregnant or breastfeeding or other ferromagnetic device/object inthe head and body within 30 cm of the treatment coil.
General medical condition, disease, or neurological disorder that interferes withthe assessments or participation.
Unable to safely withdraw, at least two weeks prior to treatment, from medicationsthat increase seizure risk.
Current substance abuse as determined by positive toxicology screen
Have a mass lesion, cerebral infarct, or other active CNS disease, including aseizure disorder.
A recent suicide attempt (defined as within the last 30 days) or presence of currentsuicidal plan or intent. Patients at risk for suicide will be required to establisha written safety plan involving their primary therapist before entering the study.
Severe impediment to vision, hearing and/or hand movement, as this is likely tointerfere with the ability to follow study protocols.
Greater than mild traumatic brain injury (defined as greater than 10 minutes loss ofconsciousness).
Taking benzodiazepines or neuroleptic medications, or any medication known to alterseizure threshold.
Acute or unstable chronic illness.
Current or lifetime history of bipolar disorder or psychosis.
Participation in another concurrent intervention-based clinical trial.
Study Design
Study Description
Connect with a study center
VA Palo Alto Health Care System
Palo Alto, California 94304
United StatesActive - Recruiting
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