Skip to content

A Retrospective Effectiveness Trial of Ketamine-Assisted Psychotherapy in Adult Patients Coping With Mental Health

Retrospective Review of Ketamine Assisted Psychotherapy Program on Mental Health at Field Trip Health Centres in North America

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05604794
Enrollment
1806
Registered
2022-11-03
Start date
2020-03-13
Completion date
2022-06-16
Last updated
2024-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Post Traumatic Stress Disorder

Keywords

ketamine, psychotherapy, mental health

Brief summary

Ketamine-Assisted Psychotherapy (KAP) is a relatively new approach for the treatment of mental health issues, which involves the combination of ketamine, a dissociative anaesthetic with psychedelic properties, and psychotherapy to promote emotional wellbeing. In this study, we investigated the effectiveness of KAP in adult patients coping with mental health. We predicted that clients would experience lasting reductions in psychological distress over time, such as depression, anxiety, and post traumatic stress, that would be detectable up to 6 months after treatment. The results of this study may provide evidence of sustained real-world effects of Ketamine-Assisted Psychotherapy, of interest to patients, clinicians, researchers, and policymakers.

Detailed description

Background: Ketamine-Assisted Psychotherapy (KAP) has shown positive effects within clinical trial settings and over short-term follow-ups, but sustained effects in real-world treatment settings remain unclear. In this study, we investigated the effectiveness of KAP in adult patients coping with mental health issues. We hypothesized that there would be significant reductions in psychological distress over time. Objective: To examine treatment effects at 1, 3, and 6 months relative to baseline on depression, anxiety, and post traumatic stress outcomes. Design: A retrospective intervention-only effectiveness trial. Setting: KAP was administered across 11 Field Trip Health clinics in North America. Intervention: KAP consisting of 4-6 guided ketamine sessions with psychotherapy-only visits after dose 1 and 2 and then after every 2 subsequent doses. Outcomes: Self-reported measures of symptoms of depression, anxiety, and post traumatic stress at 1, 3, and 6 months. Statistical Analysis: Analyses were by intention to treat. Main analysis was a mixed linear model or growth curve model to estimate change over time per outcome, yielding estimates of mean changes at each endpoint relative to baseline. Secondary analyses included evaluating case reductions (identified by cut-off values) and minimal clinically important differences (MCIDs) at each endpoint relative to baseline. Significance: This study may provide evidence of sustained real-world effects of Ketamine-Assisted Psychotherapy, of interest to patients, clinicians, researchers, and policymakers.

Interventions

COMBINATION_PRODUCTKetamine-Assisted Psychotherapy (KAP)

KAP consisting of 4-6 guided ketamine sessions with psychotherapy-only visits after dose 1 and 2 and then after every 2 subsequent doses.

Sponsors

Field Trip Health
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Written informed consent * Over the age of 18 * Should be psychologically and medically cleared by a psychiatrist, family physician, or treatment team * Diagnosed with Major Depressive Disorder (MDD), Bipolar Depression, Generalized Anxiety Disorder, Obsessive Compulsive Disorder (OCD), and Eating Disorder by a licensed healthcare practitioner (including Field Trip Consultants) * A significant history of trauma and/or formal diagnosis of PTSD as per the Diagnostic and Statistical Manual of Mental Disorders 5 (DSM 5) * Individuals who have received Electroconvulsive Therapy (ECT) or other neuromodulatory treatments like Transcranial Magnetic Stimulation (TMS) * Individuals reporting suicidal ideation may be included, as suicidal ideation is a symptom of a Major Depressive Episode (MDE)

Exclusion criteria

* Individuals who are unable to consent to the treatment * Pregnant women and nursing mothers --Note that Post Partum Depression (PPD) can be considered on a case-by-case basis in consultation with the National Medical Director. * There is a relative (not absolute) contraindication for individuals with a Body Mass Index (BMI) of above 35. These clients must be given thorough consideration by the medical team. * Any individual who has met DSM 5 criteria for a Substance Use Disorder in the past 3 months. * Note that patients with alcohol, opioid, benzodiazepine, cocaine, and amphetamine use disorders need to go through detox (for alcohol/benzodiazepines) and be sober for 4 weeks. * Note that mild active alcohol, cocaine, and cannabis use can be considered on a case-by-case basis at the comfort level of the treatment team if the client has demonstrated abstaining or significant reduction of use prior to starting treatment. * Daily use of moderate to high doses of benzodiazepines * Individuals who are experiencing psychotic symptoms as part of an MDE (mood congruent/ mood incongruent) * Psychosis: Schizophrenia, Schizoaffective disorder, Bipolar 1 with psychotic features during mania * Active Mania: Bipolar 1 (chronic non-disruptive hypomania is an exception at the discretion of the consultant) * Borderline Personality Disorder * Uncontrolled medical disorders * Physical conditions with negative interaction with ketamine (e.g., metabolic blood disorder) * Individuals with symptomatic acute brain injury within 90 days of serious injury * Individuals diagnosed with moderate to severe sleep apnea * Individuals who are unable to identify a person or service to assure their safe transport to home post treatment

Design outcomes

Primary

MeasureTime frameDescription
9-item Patient Health Questionnaire (PHQ-9)Change from 3 months compared to baselineSelf-reported measure of depression, ranging from 0-27. Higher scores are worse.
7-item Generalized Anxiety Disorder Measure (GAD-7)Change from 3 months compared to baselineSelf-reported measure of anxiety, ranging from 0-21. Higher scores are worse.
6-item PTSD Checklist (PCL-6)Change from 3 months compared to baselineSelf-reported measure of post traumatic stress, ranging from 6-30. Higher scores are worse.

Secondary

MeasureTime frameDescription
9-item Patient Health Questionnaire (PHQ-9)Change from 1 month compared to baselineSelf-reported measure of depression, ranging from 0-27.
7-item Generalized Anxiety Disorder Measure (GAD-7)Change from 1 month compared to baselineSelf-reported measure of anxiety, ranging from 0-21.
6-item PTSD Checklist (PCL-6)Change from 1 month compared to baselineSelf-reported measure of post traumatic stress, ranging from 6-30.

Countries

Canada, United States

Participant flow

Participants by arm

ArmCount
Clients
Adult patients coping with symptoms of depression, anxiety, and post traumatic stress Ketamine-Assisted Psychotherapy (KAP): KAP consisting of 4-6 guided ketamine sessions with psychotherapy-only visits after dose 1 and 2 and then after every 2 subsequent doses.
1,806
Total1,806

Baseline characteristics

CharacteristicClients
Age, Continuous42 years
STANDARD_DEVIATION 12
Race/Ethnicity, Customized
Race/Ethnicity
Missing
56 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Other Groups
441 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White
1309 Participants
Region of Enrollment
North America
1806 Participants
Sex/Gender, Customized
Gender
Female
948 Participants
Sex/Gender, Customized
Gender
Male
850 Participants
Sex/Gender, Customized
Gender
Non-binary
8 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 1,806
other
Total, other adverse events
0 / 1,806
serious
Total, serious adverse events
0 / 1,806

Outcome results

Primary

6-item PTSD Checklist (PCL-6)

Self-reported measure of post traumatic stress, ranging from 6-30. Higher scores are worse.

Time frame: Change from 3 months compared to baseline

Population: Number analysed after attrition.

ArmMeasureValue (MEAN)
Clients6-item PTSD Checklist (PCL-6)-4.24 units on a scale
Primary

7-item Generalized Anxiety Disorder Measure (GAD-7)

Self-reported measure of anxiety, ranging from 0-21. Higher scores are worse.

Time frame: Change from 3 months compared to baseline

Population: Number analysed after attrition.

ArmMeasureValue (MEAN)
Clients7-item Generalized Anxiety Disorder Measure (GAD-7)-4.80 units on a scale
Primary

9-item Patient Health Questionnaire (PHQ-9)

Self-reported measure of depression, ranging from 0-27. Higher scores are worse.

Time frame: Change from 3 months compared to baseline

Population: Number analysed after attrition.

ArmMeasureValue (MEAN)
Clients9-item Patient Health Questionnaire (PHQ-9)-3.23 units on a scale
Secondary

6-item PTSD Checklist (PCL-6)

Self-reported measure of post traumatic stress, ranging from 6-30.

Time frame: Change from 6 months compared to baseline

ArmMeasureValue (MEAN)
Clients6-item PTSD Checklist (PCL-6)-3.44 units on a scale
Secondary

6-item PTSD Checklist (PCL-6)

Self-reported measure of post traumatic stress, ranging from 6-30.

Time frame: Change from 1 month compared to baseline

ArmMeasureValue (MEAN)
Clients6-item PTSD Checklist (PCL-6)-2.14 units on a scale
Secondary

7-item Generalized Anxiety Disorder Measure (GAD-7)

Self-reported measure of anxiety, ranging from 0-21.

Time frame: Change from 1 month compared to baseline

ArmMeasureValue (MEAN)
Clients7-item Generalized Anxiety Disorder Measure (GAD-7)-2.65 units on a scale
Secondary

7-item Generalized Anxiety Disorder Measure (GAD-7)

Self-reported measure of anxiety, ranging from 0-21.

Time frame: Change from 6 months compared to baseline

ArmMeasureValue (MEAN)
Clients7-item Generalized Anxiety Disorder Measure (GAD-7)-4.10 units on a scale
Secondary

9-item Patient Health Questionnaire (PHQ-9)

Self-reported measure of depression, ranging from 0-27.

Time frame: Change from 1 month compared to baseline

ArmMeasureValue (MEAN)
Clients9-item Patient Health Questionnaire (PHQ-9)-3.23 units on a scale
Secondary

9-item Patient Health Questionnaire (PHQ-9)

Self-reported measure of depression, ranging from 0-27.

Time frame: Change from 6 months compared to baseline

ArmMeasureValue (MEAN)
Clients9-item Patient Health Questionnaire (PHQ-9)-4.74 units on a scale

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026