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Clinical Trials/NCT07171359
NCT07171359RecruitingNot Applicable

Transcranial Magnetic Stimulation (TMS) to Improve Recovery Outcomes Among Patients With Opioid Use Disorder (OUD) and Alcohol Use Disorder (AUD)

Washington State University1 site in 1 country60 target enrollmentStarted: June 1, 2027Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Engagement in Treatment As Usual Activities

Study Overview

Brief Summary

The study aims to explore the potential of Transcranial Magnetic Stimulation (TMS), particularly Theta Burst Stimulation (TBS), as an adjunctive treatment to enhance recovery outcomes (consumption and craving; withdrawal symptoms; mental, physical, sleep, and cognitive health; engagement with therapy, etc.) in individuals with Opioid Use Disorder (OUD) and individuals with Alcohol Use Disorder (AUD). This project will be completed in partnership with Another Chance Rehab (Portland): Portland's top addiction treatment program offering evidence-based treatment programs for a range of substance use disorders. Another Chance Rehab will serve as the project site for this work.

Detailed Description

The investigators will conduct a prospective, randomized, controlled trial. To identify which TMS protocol is most efficacious, there will be three arms to this study.

  1. Treatment as Usual (TAU): Participants complete their regularly scheduled therapy activities and receive no add-on TMS. They will answer the demographic survey and outcome measure surveys (listed in a later section).
  2. TAU + 3-minute TMS: Participants complete TAU as described above, with one 3-minute session of TMS TBS delivered each morning, prior to commencement of their regularly scheduled daily therapy activities, for 5 days/week, for a total of four-weeks (20 sessions total).
  3. TAU + 9-minute TMS: Participants complete TAU as described above, with one 9-minute session of TMS TBS delivered each morning, prior to commencement of their regularly scheduled daily therapy activities, for 5 days/week, for a total of four-weeks (20 sessions total).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18+ years old
  • •Enrolled in the Intensive Outpatient Program at Another Chance Drug & Alcohol Rehab Center of Portland, Portland, OR.
  • •Diagnosed with Opioid Use Disorder
  • •Diagnosed with Alcohol Use Disorder

Exclusion Criteria

  • •Children <18 years old
  • •Non-English speaking
  • •Currently taking prescription benzodiazepines or anti-convulsive medications
  • •In active alcohol or opioid withdrawal
  • •History of seizure disorder diagnosis
  • •History of Schizophrenia, Bipolar Disorder, Mania

Arms & Interventions

Treatment As Usual

No Intervention

Study participants in this arm will engage in intensive outpatient alcohol and addiction treatment provided as it usually is for all patients in this program.

3-Minute TMS

Active Comparator

TAU + 3-minute TMS: Participants complete TAU as described above, with one 3-minute session of TMS TBS delivered each morning, prior to commencement of their regularly scheduled daily therapy activities, for 5 days/week, for a total of four-weeks (20 sessions total).

Intervention: TMS Low-Dose (Device)

9-Minute TMS

Active Comparator

TAU + 9-minute TMS: Participants complete TAU as described above, with one 9-minute session of TMS TBS delivered each morning, prior to commencement of their regularly scheduled daily therapy activities, for 5 days/week, for a total of four-weeks (20 sessions total).

Intervention: TMS High-Dose (Device)

Outcomes

Primary Outcomes

Engagement in Treatment As Usual Activities

Time Frame: 4 weeks

Number of individual treatment sessions attended from baseline assessment to follow up.

Engagement in Treatment As Usual activities

Time Frame: 4 weeks

The Investigators will compare engagement in treatment as usual within and between groups by Number of Days in attendance from baseline assessment to follow up.

Secondary Outcomes

  • Delay Discounting(4 weeks)
  • Go/No-Go Task(4 weeks)
  • Balloon Analogue Risk Task(4 weeks)
  • Barratt Impulsiveness Scale-11(4 weeks)
  • Sensation Seeking Scale(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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