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Psilocybin-facilitated treatment for methamphetamine Use Disorder: A pilot study (Psi-MA)

Safety, tolerability, and feasibility of psilocybin-facilitated treatment for methamphetamine use disorder: A pilot study (Psi-MA): A pilot study (Psi-MA)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000463774
Acronym
Psi-MA
Enrollment
14
Registered
2022-03-24
Start date
2022-12-13
Completion date
2023-11-01
Last updated
2024-04-29

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

Conditions

None listed

Brief summary

This is a single centre, single arm, study primarily examining the safety and feasibility of psychotherapy combined with a single dose of 25mg psilocybin. Study Hypothesis: That psilocybin psychotherapy for methamphetamine dependence can be safely and feasibly delivered from a public addiction outpatient clinic.

Interventions

1. Three 90 minute preparatory psychotherapy sessions over two weeks facilitated by dyad of trained clinical psychologists and psychiatrist; includes alliance building, intention setting, psychoeducation and non-avoidance training. 2. Psilocybin one 25mg oral capsule within 1-2 days of the last preparatory psychotherapy session; dosing session facilitated by same therapist dyad over 8 hours following the single supervised dose. 3. Two 60 minute post-psilocybin integration psychotherapy session

1. Three 90 minute preparatory psychotherapy sessions over two weeks facilitated by dyad of trained clinical psychologists and psychiatrist; includes alliance building, intention setting, psychoeducation and non-avoidance training. 2. Psilocybin one 25mg oral capsule within 1-2 days of the last preparatory psychotherapy session; dosing session facilitated by same therapist dyad over 8 hours following the single supervised dose. 3. Two 60 minute post-psilocybin integration psychotherapy sessions facilitated by same therapist dyad; first session within 1 week of psilocybin dosing and second the following week. Intervention occurs over 4 weeks. Adherence to intervention ensured by session checklists and filming of dosing day.

Sponsors

St. Vincent's Hospital, Sydney
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
25 Years to No maximum
Healthy volunteers
No

Inclusion criteria

· Aged 25 years and above · Meet DSM-5 criteria for methamphetamine use disorder (MAUD) as determined by an Addiction Specialist · Used MA on less than 16 out of the prior 28 days · Currently seeking treatment for methamphetamine use disorder · Have at least one urine drug screen positive for methamphetamine within 1 month of trial registration · Ability to read/write in English · Availability of a friend or family member into whose care the participant can be released following their drug administration session for the subsequent 24 hours · Home-like environment in which to be cared for the 24 hours following psilocybin dosing · In good general health as assessed by detailed medical history and physical examination · Abstinence from methamphetamine, other illicit drugs (including extra-medical use of opioids and benzodiazepines), and alcohol for at least 2 days prior to psilocybin administration as confirmed via urinalysis and no signs of intoxication or withdrawal on the day of psilocybin administration · Good engagement with psychotherapy team at pre-psilocybin psychotherapy session immediately prior to psilocybin dosing session, and consensus on good alliance from both therapists. · Can swallow pills

Exclusion criteria

· Women who are pregnant or breast feeding or of childbearing potential and not willing to avoid becoming pregnant during the study · Medically significant condition which, in the opinion of the investigator would render a patient unsuitable for the study (e.g., diabetes, epilepsy, severe cardiovascular disease, hepatic or renal failure etc). · Current hypertension uncontrolled by a single antihypertensive (exceeding 140 mmHg systolic and 90 mmHg diastolic after 15 minutes of rest, averaged across four assessments on at least two separate days.) · History of psychiatric illness other than substance use disorder that is severe within the last 5 years as assessed by a psychiatrist, or any other condition that may compromise patient safety as assessed by psychiatrist · Current use of antidepressant medication, specifically monoamine oxidase inhibitors, antipsychotic medications, St. John's Wort, or other medications as determined by the study psychiatrist · Any of the following on clinical interview with a psychiatrist: o History of any drug induced psychosis or any psychotic disorder or psychotic episode o History of bipolar I or II disorder o History of anorexia nervosa or bulimia nervosa o First or second-degree relatives with history of any psychotic disorders, or bipolar I or II disorders o Current suicidal or homicidal ideation · History of any other illicit drug, illicit or prescribed benzodiazepine use extra-medical use of opioids within the 2 days preceding psilocybin administration. People receiving opioid substitution therapy who otherwise meet the eligibility criteria may be included. · History of alcohol use disorder within the preceding 3 months · History of cannabis use disorder within the preceding 3 months · Use of a classical hallucinogen (LSD, DMT, psilocybin, mescaline, salvia divinorum, ibogaine) within the preceding 28 days. · Planning to move from the Sydney area in the next 6 months or any other reason precluding follow up in this time period (e.g. likely travel or imprisonment) · Contraindications of MRI (metallic objects in the body, claustrophobia, difficulty with prior MRI) · Unstable housing or homeless · Inability to attend all screening visits

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026