Repetitive Transcranial Magnetic Stimulation Treatment of Stimulant Use Disorder
Key facts
- Who runs it
- VA Office of Research and Development
- Where
- Palo Alto, United StatesSee the site
- Trial code
- Status
- Recruiting
- People taking part
- 106 people, planned
- Started
- 1 May 2026
- Expected to end
- 31 Dec 2029
- Type of study
- Interventional, 2 groupsOne group gets a sham (pretend) treatment, for comparison.
- Treatments tested
- Repetitive transcranial magnetic stimulation (rTMS)
- Sham rTMS
- Record updated
- 11 September 2026
Who can take part
- Age
- 18 years to 65 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 15 criteriaShow less
Who can take part
- Must be a U.S. Veteran
- Structured Clinical Interview for DSM Disorders (SCID) confirmed diagnosis of SUD, severe
- Last use of stimulants >2 and <8 weeks
- Stable medication regimen (no change in dose or agents between 2 weeks prior to the start of and throughout the treatment phase of the study)
- Stable medical health
Who cannot take part
- History of prior adverse reaction to Transcranial magnetic stimulation (TMS)
- Implants or medical devices incompatible with TMS
- For subjects participating in functional magnetic resonance imaging (fMRI) scans, presence of ferromagnetic material in their body or taking DAergic medications
- On medications thought to significantly lower seizure threshold, e.g. clozapine, chlorpromazine, clomipramine, and bupropion > 400mg/day
- Seizure disorder or conditions known to substantially increase risk for seizures
- Acute or unstable chronic medical illness that would affect participation or compliance in the study, e.g. unstable angina
- Unstable psychiatric symptoms that precludes consistent participation in the study, e.g. active current suicidal intent or plan; severe psychosis
- Other substance use disorder not in remission
- Chronic or recurring Axis I psychotic disorders
- Pregnant or lactating female
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 65 years old?
Where in United States
- VA Palo Alto Health Care System, Palo Alto, CAPalo Alto, United StatesContact: Jong H Yoon, MDTaking people
About the trial
What the trial wants to find out
The purpose of this study is to establish a new treatment (repetitive transcranial stimulation (rTMS)) for Veterans with stimulant use disorder (SUD). Despite the large public health burden imposed by SUD, there is currently no FDA-approved or widely recognized effective somatic treatment. This placebo controlled study will test the effectiveness of rTMS in the treatment of SUD, and explore biomarkers that may guide patient selection for rTMS treatment and predict treatment response.
The 2 groups in the trial
- Active rTMSTreatment being tested
Receive active rTMS
Treatment: Repetitive transcranial magnetic stimulation (rTMS)
- Sham rTMSSham treatment, for comparison
Receive sham rTMS
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Fit questions
- Built from NCT07112105, who can take part
- Record updated
- 11 September 2026