Magnetic Seizure Therapy for Schizophrenia - Trial

Last updated: January 30, 2026
Sponsor: Centre for Addiction and Mental Health
Overall Status: Active - Recruiting

Phase

N/A

Condition

Mood Disorders

Tourette's Syndrome

Schizophrenia And Schizoaffective Disorders (Pediatric)

Treatment

Electroconvulsive Therapy (ECT)

Magnetic Seizure Therapy (MST)

Clinical Study ID

NCT06672588
2105
  • Ages > 18
  • All Genders

Study Summary

This trial aims to assess the clinical effects and tolerability of Magnetic Seizure Therapy (MST) as an alternative to electroconvulsive therapy (ECT) for Treatment Resistant Schizophrenia (RS).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. are inpatients or outpatients;

  2. demonstrate capacity to consent according to the MacArthur competence assessmenttool for clinical research (MacCAT-CR);

  3. have a DSM-5 diagnosis of Schizophrenia or Schizoaffective Disorder for at least 2years, as determined by the MINI International Neuropsychiatric Interview - Version 7 (MINI-7.0);

  4. are 18 years of age or older;

  5. have demonstrated resistance to at least 2 antipsychotics of 600 mg ofchlorpromazine equivalents for at least 6 weeks;

  6. have a BPRS score at baseline of at least moderate severity (>4) on one of thefour psychotic items (i.e., hallucinatory behavior, suspiciousness, conceptualdisorganization, unusual thought content) or at least 12 on these 4 items combined;

  7. are considered to be appropriate to receive convulsive therapy as assessed by an ECTattending psychiatrist and a consultant anaesthesiologist;

  8. are on an antipsychotic at an adequate dose and are agreeable to keeping theircurrent antipsychotic treatment constant during the acute phase of the intervention;

  9. are able to adhere to the intervention schedule;

  10. meet the MST safety criteria;

  11. If a woman of child-bearing potential: is willing to provide a negative pregnancytest and agrees not to become pregnant during trial participation.

Exclusion

Exclusion Criteria:

  1. have a history of MINI diagnosis of a substance use disorder (other than nicotineand caffeine) within the past three months;

  2. have a concomitant major unstable medical illness;

  3. are pregnant or intend to get pregnant during the study;

  4. have probable dementia based on study investigator assessment;

  5. have any significant neurological disorder or condition likely to be associated withincreased intracranial pressure or a space occupying brain lesion, e.g., cerebralaneurysm;

  6. present with a serious medical condition,

  7. have an intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlearimplants, or electrodes) or any other metal object within or near the head,excluding the mouth, that cannot be safely removed;

  8. require a benzodiazepine with a dose > lorazepam 2 mg/day or equivalent or anyanticonvulsant due to the potential of these medications to limit the efficacy ofboth MST and ECT;

  9. are unable to communicate in English fluently enough to complete theneuropsychological tests;

  10. have a non-correctable clinically significant sensory impairment (i.e., cannot hearor see well enough to complete the neuropsychological tests).

Study Design

Total Participants: 80
Treatment Group(s): 2
Primary Treatment: Electroconvulsive Therapy (ECT)
Phase:
Study Start date:
April 22, 2025
Estimated Completion Date:
November 30, 2028

Study Description

The study will involve a randomized, double blind, non-inferiority clinical trial with two treatment arms conducted in two academic institutions (the Centre for Addiction and Mental Health (CAMH) in Toronto, and University of British Columbia (UBC) Hospital in Vancouver, British Columbia). The investigators will compare MST to right unilateral ultrabrief pulse ECT (RUL-UB-ECT). Treatment will be administered two to three days per week. Clinical response will be assessed with the 18-item Brief Psychiatric Rating Scale (BPRS). Response will be defined as greater than or equal to 40% decrease in the BPRS positive psychotic symptom subscale (4 items - hallucinatory, behavior, suspiciousness, conceptual disorganization, and unusual thought content). Patients who do not meet response criteria after 15 treatment sessions will be considered non-responders and will cease treatment sessions. The blind will not be broken to participants until the completion of the entire study.

Connect with a study center

  • University of British Columbia Hospital

    Vancouver, British Columbia V6T 2A1
    Canada

    Site Not Available

  • University of British Columbia Hospital

    Vancouver 6173331, British Columbia 5909050 V6T 2A1
    Canada

    Active - Recruiting

  • Centre for Addiction and Mental Health

    Toronto, Ontario M6J 1H4
    Canada

    Site Not Available

  • Centre for Addiction and Mental Health

    Toronto 6167865, Ontario 6093943 M6J 1H4
    Canada

    Active - Recruiting

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