Phase
Condition
Mood Disorders
Tourette's Syndrome
Schizophrenia And Schizoaffective Disorders (Pediatric)
Treatment
Electroconvulsive Therapy (ECT)
Magnetic Seizure Therapy (MST)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
are inpatients or outpatients;
demonstrate capacity to consent according to the MacArthur competence assessmenttool for clinical research (MacCAT-CR);
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);
are 18 years of age or older;
have demonstrated resistance to at least 2 antipsychotics of 600 mg ofchlorpromazine equivalents for at least 6 weeks;
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;
are considered to be appropriate to receive convulsive therapy as assessed by an ECTattending psychiatrist and a consultant anaesthesiologist;
are on an antipsychotic at an adequate dose and are agreeable to keeping theircurrent antipsychotic treatment constant during the acute phase of the intervention;
are able to adhere to the intervention schedule;
meet the MST safety criteria;
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:
have a history of MINI diagnosis of a substance use disorder (other than nicotineand caffeine) within the past three months;
have a concomitant major unstable medical illness;
are pregnant or intend to get pregnant during the study;
have probable dementia based on study investigator assessment;
have any significant neurological disorder or condition likely to be associated withincreased intracranial pressure or a space occupying brain lesion, e.g., cerebralaneurysm;
present with a serious medical condition,
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;
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;
are unable to communicate in English fluently enough to complete theneuropsychological tests;
have a non-correctable clinically significant sensory impairment (i.e., cannot hearor see well enough to complete the neuropsychological tests).
Study Design
Study Description
Connect with a study center
University of British Columbia Hospital
Vancouver, British Columbia V6T 2A1
CanadaSite Not Available
University of British Columbia Hospital
Vancouver 6173331, British Columbia 5909050 V6T 2A1
CanadaActive - Recruiting
Centre for Addiction and Mental Health
Toronto, Ontario M6J 1H4
CanadaSite Not Available
Centre for Addiction and Mental Health
Toronto 6167865, Ontario 6093943 M6J 1H4
CanadaActive - Recruiting

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