Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06424184

Substance Use Disorder Treatment With Accelerated Repetitive Transcranial Magnetic Stimulation for Depression

Led by University of Texas Southwestern Medical Center · Updated on 2025-07-31

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying an accelerated form of repetitive transcranial magnetic stimulation (rTMS) for people with depression and stimulant use disorder, including methamphetamine or cocaine use disorder. This is a small, open-label feasibility trial aiming to understand how well this accelerated rTMS treatment can be given and tolerated in this group. The study is sponsored by the University of Texas Southwestern Medical Center and involves participants already enrolled in an ongoing stimulant use disorder study. Participants who qualify will receive up to 50 sessions of rTMS over three weeks, with up to four short sessions each day and up to five days per week. The sessions use intermittent theta burst stimulation targeting the left dorsolateral prefrontal cortex. A follow-up visit is scheduled one week after the final rTMS session to monitor progress. During the study, participants will undergo EEG and ECG tests, urine drug screens, and complete both self-report and clinician-rated assessments related to stimulant use, craving, depression, irritability, and suicidality. Researchers will measure how feasible the accelerated rTMS course is, its effects on stimulant use and craving, and changes in symptoms over the treatment and follow-up periods. Total participation lasts approximately four weeks including treatment and follow-up.

CONDITIONS

Brief Title

Accelerated rTMS for Substance Use Disorder and Depression

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be aged 18 to 65 years, inclusive
  • Able to understand, speak, and read English and willing to comply with study procedures
  • Self-report stimulant use (cocaine, methamphetamine, or prescription stimulants) at least 10 days in the 30 days before consent
  • Diagnosed with moderate or severe Cocaine or Methamphetamine Use Disorder or other Stimulant Use Disorder in the past 12 months
  • Have a PHQ9 score of 5 or higher
  • Willing to provide urine samples, EEGs, and ECGs
  • Willing to use birth control during the treatment phase if of childbearing potential
Not Eligible

You will not qualify if you...

  • Current use of alcohol, benzodiazepines, or other sedative/hypnotics that precludes safe participation
  • Serious medical disorders making participation unsafe or preventing data collection
  • History of unprovoked seizure or seizure in past 6 months
  • History of brain lesions or tumors
  • Metal implants or non-removable metal objects above the neck
  • Current pregnancy
  • Current or lifetime manic or hypomanic episode
  • Current psychotic disorder
  • Being a prisoner or in police custody at screening

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

screening and enrollment visit

Implementation

Duration - Up to 3 weeks

Participants receive an accelerated course of repetitive Transcranial Magnetic Stimulation (rTMS) consisting of up to 4 sessions per day, up to 5 days per week, for a total of 50 sessions over three weeks.

Daily visits up to 5 days per week for up to 3 weeks

Follow-up

Duration - 1 week

Participants return for a follow-up visit one week after completing the rTMS sessions for assessments.

1 visit (in-person) one week post-treatment

Trial Site Locations

Total: 1 location

1

UT Southwestern Medical Center

Dallas, Texas, United States, 75247

Actively Recruiting

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Research Team

T

Taylor Helmbrecht, B.S.A.

T

Teresa Slettebo, B.A.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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