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Can pairing ketamine with talk therapy beat depression alone?
NCT ID NCT07801703
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether adding behavioral activation therapy to intravenous ketamine helps people with treatment-resistant depression more than ketamine alone. Adults aged 18 to 65 who have not improved with at least two antidepressants will receive ketamine infusions twice weekly for three weeks. Half will also attend therapy sessions during that time. Those who respond will continue both treatments for an additional 12 weeks, and researchers will compare changes in depression symptoms and daily functioning between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intravenous ketamine combined with behavioral activation therapy
- What this could lead to
- If the combination works, it could offer a more effective treatment strategy for people with treatment-resistant depression, improving symptoms and daily functioning beyond ketamine alone.
- What could go wrong
- This is a mid-stage trial with only 60 participants, so results may not apply broadly. Ketamine can cause side effects like dissociation or blood pressure changes, and adding therapy may not boost outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. English speaking 2. Age 18-65 at Screening 3. Meeting criteria for major depressive disorder (MDD), in a major depressive episode without psychotic symptoms according to the Diagnostic and Statistical Manual for Mental Disorders (DSM-5) 4. Have not responded adequately to at least two separate courses of treatment with different antidepressants, each of adequate dose and duration, in the current depressive episode 5. Currently in a moderate to severe depressive episode, with a minimum MADRS score of ≥22 at Screening 6. Be under the care of a designated health care provider (e.g., family physician or psychiatrist) to follow their care after the completion of the study 7. Willing to maintain stable doses of concomitant psychotropic medications throughout the study 8. Willing to abstain from taking prohibited medications on the days of treatment (i.e., for 12 hours prior to treatment) as per study physician instruction (e.g., benzodiazepines, cannabis) 9. Able to secure a ride/chaperone home from all ketamine infusions. Exclusion Criteria: 1. Body mass index (BMI) ≥35 2. Depression secondary to a stroke, cancer, or other clinically significant medical illness, per study physician judgement 3. Not medically cleared to receive ketamine treatment due to presence of clinically relevant disease, per study physician judgement (e.g., uncontrolled hypertension, renal or hepatic impairment, significant coronary artery disease, vascular disease, diabetes mellitus, seizure disorder, intracerebral hemorrhage, history of cerebrovascular accident \[CVA\]) 4. Pregnant, breastfeeding or of childbearing potential and unwilling to use an approved method of contraception during the study, as assessed during the Screening Visit medical clearance 5. History of a primary psychotic disorder (e.g., schizophrenia), or current or recent (\<2 years) acute episode of psychosis 6. Current and/or recent history (\<12 months) of substance use disorder/dependence (except for alcohol, cannabis, caffeine or nicotine) as defined by DSM-5 criteria 7. Current and/or recent history (\<6 months) of cannabis use disorder as defined by DSM-5 criteria, or unable to abstain from using cannabis 12 hours before and 12 hours after each ketamine infusion 8. Current and/or recent history (\<6 months) of alcohol use disorder as defined by DSM-5 criteria, or unable to abstain from using alcohol 12 hours before and 12 hours after each ketamine infusion 9. Concurrent use of ketamine or psychedelics in any form 10. A previous history or known diagnosis of major neurocognitive disorder 11. Known or suspected history of intolerance, allergy or hypersensitivity to ketamine 12. Any other condition or circumstance that, in the opinion of the QI/study physicians, would adversely affect the participant's ability to complete the study procedures or its measures 13. Concurrent psychotherapy treatment outside the clinical trial. A participant may opt to pause or terminate their current ongoing psychotherapy to participate in the study, at their own discretion. 14. Concurrent active electroconvulsive therapy (ECT) or repetitive transcranial magnetic stimulation (rTMS) therapy.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The Royal
Ottawa, Ontario, K1Z 7K4, Canada
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