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Grant: Project Grant

University of Calgary

$1,143,675.00

A randomized placebo-controlled trial of pharmacologically enhanced transcranial magnetic stimulation to decrease suicide risk.

EF 2025-26

Résumé
Suicide is the most severe outcome in mental illness and remains of the greatest public health challenges. Unfortunately, despite years of successful prevention initiatives suicide rates have plateaued in Canada. New ways of treating and preventing suicide are urgently needed. One strategy is to target specific circuits in the brain using non-invasive neurostimulation interventions such as transcranial magnetic stimulation (TMS). TMS is well established in the treatment of Major Depression, and has been shown to reduce suicidal ideation. Yet, this treatment typically involves daily interventions over weeks to have effect, and benefit from treatment is not guaranteed. Those at risk of suicide cannot afford to wait weeks for an uncertain benefit. Our compelling pilot data suggests that by pairing stimulation with a small molecule, DCycloserine, suicide risk resolves rapidly. Indeed, suicidal ideation quickly decreases in severity and performance on computerized tests of implicit suicide risk improve. This is important, because these tests use implicit association to capture whether the person aligns themselves more strongly with life or with death/suicide and performance on the test is associated with future suicidal behavior. It is possible, therefore, that this intervention could not only treat acute suicide risk but also change trajectories of suicidal behavior. We propose to conduct a clinical trial in individuals who are at the highest risk for suicide, namely individuals who have previously survived a suicide attempt and who are currently suicidal. Individuals will be randomized to receive an accelerated form of TMS in which treatments are delivered twice daily paired with either a placebo or D-Cycloserine to determine the effect on suicidal ideation, implicit suicide risk, and suicidal ideation in the 6 months following treatment. The results of this study may provide a new means of decreasing suicide risk.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
532467
Name
Mcgirr Alexander
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Behavioural Sciences - B-2
Projecttitle
A randomized placebo-controlled trial of pharmacologically enhanced transcranial magnetic stimulation to decrease suicide risk.
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$1,143,675
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Depression; Nmda Receptor; Suicide; Transcranial Magnetic Stimulation
Abstract
Suicide is the most severe outcome in mental illness and remains of the greatest public health challenges. Unfortunately, despite years of successful prevention initiatives suicide rates have plateaued in Canada. New ways of treating and preventing suicide are urgently needed. One strategy is to target specific circuits in the brain using non-invasive neurostimulation interventions such as transcranial magnetic stimulation (TMS). TMS is well established in the treatment of Major Depression, and has been shown to reduce suicidal ideation. Yet, this treatment typically involves daily interventions over weeks to have effect, and benefit from treatment is not guaranteed. Those at risk of suicide cannot afford to wait weeks for an uncertain benefit. Our compelling pilot data suggests that by pairing stimulation with a small molecule, DCycloserine, suicide risk resolves rapidly. Indeed, suicidal ideation quickly decreases in severity and performance on computerized tests of implicit suicide risk improve. This is important, because these tests use implicit association to capture whether the person aligns themselves more strongly with life or with death/suicide and performance on the test is associated with future suicidal behavior. It is possible, therefore, that this intervention could not only treat acute suicide risk but also change trajectories of suicidal behavior. We propose to conduct a clinical trial in individuals who are at the highest risk for suicide, namely individuals who have previously survived a suicide attempt and who are currently suicidal. Individuals will be randomized to receive an accelerated form of TMS in which treatments are delivered twice daily paired with either a placebo or D-Cycloserine to determine the effect on suicidal ideation, implicit suicide risk, and suicidal ideation in the 6 months following treatment. The results of this study may provide a new means of decreasing suicide risk.
Competitiondate
202509
Approvedterm2
6 yrs 0 mth
Pinamesdelim
Mcgirr, Alexander
Approvedterm
6 ans 0 mois
Cihrcontribution2
~ $1,143,675~ $0~