Transcranial Magnetic Stimulation for Nicotine Dependence: An Effectiveness-Implementation Trial

Last updated: July 31, 2024
Sponsor: Centre for Addiction and Mental Health
Overall Status: Active - Not Recruiting

Phase

4

Condition

Stimulant Use Disorder

Tourette's Syndrome

Kleptomania

Treatment

Brainsway H4 deep Repetitive Transcranial Magnetic Stimulation (rTMS) coil

Nicotine replacement

Clinical Study ID

NCT06534047
2024-018
  • Ages 18-70
  • All Genders

Study Summary

Tobacco smoking is the leading preventable cause of morbidity and mortality worldwide. However, currently available treatments, including standard pharmacotherapy and behavioural support, are limited in their efficacy, tolerability, and acceptability by patients. Additionally, tobacco use is substantially higher in individuals with comorbid mental illness, constituting a particularly vulnerable population. As such, the development of multiple evidence-based treatments for smoking cessation is of upmost importance.

Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive brain-based approach in which alternating magnetic fields are applied to the scalp to induce electrical currents in cortical tissue. As it can modulate neural circuits implicated in neuropsychiatric disorders, it is a promising brain-based approach in the treatment of substance use disorders. Recently, a deep TMS coil has been cleared by the Food and Drug Administration (FDA) as efficacious for tobacco use disorder, representing the first rTMS indication for addictions. Before adoption of this intervention into smoking cessation clinics, it is important to investigate whether implementation of rTMS into clinical care is feasible, acceptable, and appropriate for patients receiving care for nicotine dependence.

The objective of this study is to compare the effectiveness of rTMS versus treatment as usual for patients with psychiatric disorders seeking treatment for smoking cessation. Also, barriers to the implementation of rTMS in routine clinical care will be examined by speaking with patients and health care providers on their experience with rTMS.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patient Participants:

The patient participant must meet all the inclusion criteria to be eligible for this study:

  1. Able to provide informed consent.

  2. Age 18-70.

  3. Self-reported daily tobacco cigarette consumption.

  4. Meet DSM-5 criteria for a psychiatric disorder that includes one of the following:mood disorders (e.g. major depressive disorder, bipolar disorder), anxiety disorders (e.g. panic disorder, social anxiety disorder), psychotic disorders (e.g.schizophrenia), posttraumatic stress disorder, obsessive compulsive disorders, orother substance use disorders (e.g. alcohol use disorder) as determined by theStructured Clinical Interview for DSM-5 Disorders, Research Version (SCID-5 RV).

  5. Interested in using either Repetitive Transcranial Magnetic Stimulation (rTMS) ornicotine replacement therapy as a smoking cessation treatment.

  6. Intending on quitting smoking within the next 30 days.

Exclusion

Exclusion Criteria:

Patient Participants:

  1. Contraindication to rTMS according to the TMS Adult Safety Screen (TASS) and PIreview.

  2. Have any intracranial implant (e.g., aneurysm clips) or any other metal objectwithin or near the head, excluding the mouth, that cannot be safely removed.

  3. Pregnant or intending to be pregnant during the study.

  4. A history of a primary seizure disorder, seizure associated with an intracraniallesion, recurrent seizures related to substance intoxication or withdrawal or recentseizure within the last 6 months.

  5. Space occupying intracranial lesion.

  6. Any generalized skin disorders precluding the use of the nicotine patch.

  7. Any known hypersensitivity or allergies to the nicotine patch.

  8. Any known life-threatening arrhythmias or severe/worsening angina pectoris.

  9. Within two weeks of experiencing a myocardial infarction or cerebral vascularaccident.

  10. Currently using or has used nicotine replacement therapy within the past two weeks.

  11. Diagnosed with a terminal illness

  12. Current regular use of e-cigarettes or other vaping devices containing nicotine andnot willing to stop using these devices for the duration of the study.

  13. Acutely unstable medical, psychiatric, or substance use disorder comorbidity withsafety concerns at the discretion of the PI or study physician.

  14. Previous treatment with rTMS for smoking cessation

  15. Treatment with nicotine replacement therapy anytime within the last 1 month

Study Design

Total Participants: 40
Treatment Group(s): 2
Primary Treatment: Brainsway H4 deep Repetitive Transcranial Magnetic Stimulation (rTMS) coil
Phase: 4
Study Start date:
September 01, 2024
Estimated Completion Date:
September 01, 2026

Study Description

The objective is to pilot a pragmatic, randomized, comparative effectiveness trial of rTMS, compared to treatment as usual (TAU), for smoking cessation in individuals with psychiatric comorbidities, using a type 1 hybrid effectiveness-implementation design. Participants will be included if they meet DSM-5 criteria for mood disorders, anxiety disorders, psychotic disorders, posttraumatic stress disorder, obsessive compulsive disorders, or other substance use disorders. Those that undergo rTMS treatment will be offered open-label rTMS treatment with the FDA and Health Canada approved Brainsway deep TMS (dTMS) coil which includes 3 weeks of daily on-site rTMS treatments followed by 3 weeks of weekly treatments. Those that undergo TAU will receive nicotine replacement therapy and counselling through the supervision of a study physician.