RecruitingPhase 2NCT06480500

i-CBT and IV Ketamine for Suicidality in Treatment-Resistant Depression: A Randomized, Midazolam-Controlled Clinical Trial

Integrated Internet-Based Cognitive Behavioural Therapy (i-CBT) and Intravenous Ketamine for Suicidality in Treatment-Resistant Depression: A Randomized, Midazolam-Controlled Clinical Trial


Sponsor

University Health Network, Toronto

Enrollment

110 participants

Start Date

Jan 2, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Approximately four thousand Canadians die by suicide every year, and suicide is the second leading cause of death in youth and young adults (15-34 years). Most people with depression experience thoughts of suicide and many will also plan and/or attempt suicide at some time in their life. There is an urgent need for new scalable treatments that can effectively reduce suicidality in people with depression. Cognitive behavioural therapy (CBT) reduces suicidal thoughts and behaviours, and can be delivered through the internet (i-CBT) making it more accessible and scalable. However, i-CBT has not been shown to rapidly reduce suicidal thoughts and behaviours (suicidality), such as within 24 hours. IV ketamine on the other hand has been shown to rapidly reduce thoughts of suicide, but not suicidal behaviours. Therefore, combining i-CBT with IV ketamine may be more effective reducing suicidality than i-CBT treatment with a control treatment. The investigators propose a 13-week, multi-site, study that looks at how combining i-CBT and IV ketamine treatment will affect suicidality in individuals with depression who have recently experienced suicidal thoughts and/or behaviours, but have not responded to previous treatment. All 110 participants will receive a weekly session of i-CBT for 13 weeks, but half will be randomly assigned to also receive six IV ketamine treatments or six IV midazolam treatments (control treatment) over the first initial 30 days. The investigators will measure changes in suicidal thoughts and behaviours before drug treatment and at the primary endpoint (i.e.,day 30), and after 3 months (i.e. Day 91) of the starting treatment.


Eligibility

Min Age: 21 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a combination of IV ketamine (a fast-acting treatment for depression) and internet-based cognitive behavioral therapy (iCBT) can reduce suicidal thoughts in people with treatment-resistant depression — meaning depression that hasn't responded to other treatments. **You may be eligible if...** - You are 21–65 years old - You have been diagnosed with Major Depressive Disorder (MDD) with a current moderate-to-severe episode - You currently have thoughts of suicide or self-harm - Your depression has not responded to at least two different antidepressants - You are able to give your own informed consent **You may NOT be eligible if...** - You have a psychotic disorder or symptoms alongside your depression - You have an active or serious medical condition that could interfere with treatment - You are pregnant or breastfeeding - You are unable to commit to the full study schedule Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGKetamine hydrochloride

55 patients will receive ketamine hydrochloride, over six infusions, flexibly dosed between 0.5 mg/kg to 0.85 mg/kg.

BEHAVIORALi-CBT (Internet-based Cognitive Behavioural Therapy)

Each week for 13 weeks, participants will watch an online module that last approximately 45-50 mins each, with homework at the end of each module. Homework is submitted and reviewed by a therapist, who will provide personalized feedback before progression to the next module.

DRUGMidazolam Hydrochloride

55 patients will receive midazolam hydrochloride, over six infusions, flexibly dosed between 0.02 mg/kg to 0.035 mg/kg.


Locations(1)

Toronto General Hospital

Toronto, Ontario, Canada

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NCT06480500


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