Clinical trial

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

Name
2022-3067-11240-5
Description
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.
Trial arms
Trial start
2020-03-13
Estimated PCD
2022-06-16
Trial end
2022-06-16
Status
Completed
Phase
Early phase I
Treatment
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.
Arms:
Clients
Size
1806
Primary endpoint
9-item Patient Health Questionnaire (PHQ-9)
Change from 3 months compared to baseline
7-item Generalized Anxiety Disorder Measure (GAD-7)
Change from 3 months compared to baseline
6-item PTSD Checklist (PCL-6)
Change from 3 months compared to baseline
Eligibility criteria
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
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 1806, 'type': 'ACTUAL'}}
Updated at
2024-03-20

1 organization

2 products

3 indications

Indication
Anxiety
Organization
Field Trip Health