Ketamine-Assisted Psychotherapy for Treatment-Resistant Depression

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Rochester

About this trial

The goal of this clinical trial is to understand the effect of ketamine on the brain in people with treatment-resistant depression (TRD). TRD occurs in around a third of people with depression and leads to higher suicide rates compared to those with major depressive disorder. A desperate need for a rapid acting antidepressant drug (RAAD) is needed to help improve quality of life for people with TRD. Ketamine has been shown to be a RAAD, and esketamine (a form of ketamine) was approved by the FDA to treat TRD. Ketamine has been known to cause dissociative experiences, that can lead to an increase in the "Openness to Experience" personality trait and psychological flexibility that occurs at "peak experience". This has been shown to improve mental health conditions and lower suicide risk. This study aims to further understand if there is a connection between this new change of mind and changes in brain activity. Ketamine has been shown to improve brain plasticity as well, specifically in the frontolimbic region of the brain, an area associated with depression. The investigators are analyzing the brain using functional magnetic resonance imaging (fMRI), a method used to measure brain activity. The frontolimbic region is also associated with cognitive flexibility and emotional processing, an important hurdle in treating TRD. Due to this, the investigators are pairing the ketamine treatment with psychotherapy sessions, to guide the processing experience, which can lead to higher emotional flexibility.

The main questions this study aims to answer are:

* Are frontolimibic plasticity circuitry changes associated with openness to experience and peak experience? * Is it feasible to recruit and retain people through a two-month KAP study? * Is the structure of the study effective for treating TRD?

Participants will:

* Visit the facilities 6-8 times * Complete 2 MRI brain scans * Complete 3-4 psychotherapy sessions * Receive 1-2 doses of ketamine * Complete online surveys between 3-4 visits

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18 years old or older

Able to speak, read, and understand English

In generally stable health

Must have treatment resistant depression, as defined as scoring in the moderate or above range on the HDRS and having failed two adequate trials of antidepressants in the last two years.

Disqualifiers

Uncontrolled hypertension

Impaired cardiac status

Chronic Obstructive Pulmonary Disease

Congenital Long QT Syndrome

Trial design

Design model

Single group

Treatments tested in this trial

  • Ketamine hydrochloride injection

    Drug

    0.5-1mg/kg intramuscular (IM) injection of ketamine

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: TRD groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Proportion of Participants Retained in Study Through 2-Month Follow-Up

Retention will be assessed as completion of all scheduled study assessments through the 2-month follow-up. A single value is derived for each participant, coded as 1 (retained) or 0 (not retained). Higher values indicate successful retention; lower values indicate dropout.

Time frame
2 months post-enrollment
2

Mean Change in Hamilton Depression Rating Scale (HDRS) Total Score

Depression severity will be measured using the 17-item HDRS (items scored 0-2 or 0-4; total score range 0-52). A single value is derived by summing item scores. Higher scores indicate greater depression severity (worsening); lower scores indicate reduced severity (improvement). Mean change is calculated as post-treatment score minus baseline score.

Time frame
Baseline, once a day for up to 7 days after baseline, within 90 minutes after ketamine dosing session, once a day for up to 7 days after ketamine dosing session, once a day up to 7 days before 2-month follow-up, and at 2-month follow-up

Secondary outcomes

1

Mean Change in Numerical Pain Rating Scale Score

Pain intensity will be assessed using an 11-point Numeric Rating Scale (0 = no pain, 10 = worst imaginable pain). A single value is derived by averaging participant ratings at each time point. Higher scores indicate worse pain; lower scores indicate reduced pain. Mean change is calculated as follow-up score minus baseline score.

Time frame
Baseline, once a day for up to 7 days after baseline, within 90 minutes after ketamine dosing session, once a day for up to 7 days after ketamine dosing session, once a day up to 7 days before 2-month follow-up, and at 2-month follow-up
2

Mean Change in NEO Five-Factor Inventory-3 (NEO-FFI-3) Openness Subscale Score

Openness will be measured using the NEO-FFI-3 Openness subscale (12 items scored 0-4; total score range 0-48). A single value is derived by summing the 12 item scores. Higher scores indicate greater openness; lower scores indicate reduced openness. Mean change is calculated as follow-up score minus baseline score.

Time frame
Baseline and 2-month follow-up.
3

Mean Acceptability Rating of Ketamine-Assisted Psychotherapy

Acceptability will be assessed using a 5-point Likert scale (1 = low acceptability, 5 = high acceptability). A single value is derived by averaging scores across participants. Higher scores indicate greater acceptability; lower scores indicate lower acceptability.

Time frame
At 2 month follow-up
4

Proportion of Participants Reporting Adverse Events (AEs)

Adverse events will be graded using the Common Terminology Criteria for Adverse Events (CTCAE v5.0; 0 = none, 1 = mild, 2 = moderate, 3 = severe, 4 = life-threatening, 5 = fatal). A single value is derived for each participant as the highest AE grade experienced. Higher values indicate more severe AEs; lower values indicate milder or no AEs.

Time frame
Throughout the 8-week study.

Other outcomes

1

Mean Mystical Experience Questionnaire (MEQ-30) Total Score

Mystical experiences will be measured using the MEQ-30 (30 items scored 0-5; total score range 0-150). A single value is derived by summing item scores. Higher scores indicate more intense mystical experiences; lower scores indicate fewer or weaker mystical experiences.

Time frame
within 1-2 days after each ketamine dosing session
2

8. Mean Change in Resting-State fMRI Whole Brain Functional Connectivity

Functional connectivity will be measured using resting-state fMRI. Correlations between 400 cortical ROIs (Schaefer atlas) and subcortical ROIs (Harvard-Oxford atlas) will be calculated. A single value per participant is derived as the mean Fisher-Z transformed correlation coefficient across all ROI pairs. Higher values indicate stronger connectivity; lower values indicate weaker connectivity. Mean change is calculated as post-treatment value minus baseline value.

Time frame
Baseline and at 2 month follow-up
3

Mean Change in Subcortical Brain Volume

Volumes of subcortical structures will be calculated from MRI scans using FSL-FIRST and FreeSurfer. A single value per participant is derived by summing the volumes of predefined structures (mm³). Higher values indicate larger volumes; lower values indicate smaller volumes. Mean change is calculated as post-treatment volume minus baseline volume.

Time frame
Baseline and at 2 month follow up
4

Clinician-Administered Dissociative States Scale (CADSS-6) Total Score

Dissociation will be measured using the CADSS-6 (6 items scored 0-4; total score range 0-24). A single value is derived by summing item scores. Higher scores indicate greater dissociation; lower scores indicate less dissociation.

Time frame
within 90 minutes after each ketamine dosing session

Sponsors and contacts

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