About this trial
Up to 40% of individuals with alcohol use disorder (AUD) experience depression, which increases the risk of early relapse. Depression can cause relapse to occur 3 times faster in individuals with AUD who experience depressive symptoms at discharge. No treatments have been approved for individuals with both AUD and depression. Psilocybin, a psychedelic, shows promising results in treating both depression and addiction. It may be particularly effective for preventing relapse in people with AUD who also have depressive symptoms after detoxification, offering quicker action than traditional antidepressants.
The Psilocybin Alcohol Depression (PAD) pilot study, launched in February 2024, has provided critical insights for avoiding methodological flaws and demonstrated that psilocybin-assisted psychotherapy (PAP) is both feasible and acceptable. Preliminary efficacy analyses were conducted: at 12 weeks, the 25 mg group showed significantly greater reductions in drinking days (p = 0.038) and craving frequency (p = 0.045). Relapse rates were 35% in the 25 mg group and 50% in the control group (HR = 0.52 \[0.16-1.65\]). In the ERPPAD trial, the study authors will compare high-dose PAP with low-dose PAP in preventing relapse in individuals with AUD and depressive symptoms. The hypothesis is that high-dose PAP will be more effective than low-dose in preventing relapse over 6 months.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Confirmed DSM-5 diagnosis of severe AUD.
Scale BDI-II ((Beck Depression Inventory) ≥14
The last drink must have been consumed between day(D) -60 and D -10 at the inclusion visit. The patient must have had at least 1 HDD during the last drinking period NB: The last drinking period before inclusion is defined by the last 4 weeks counted from the last drink.
The patient must have given their free and informed consent and signed the consent form
Disqualifiers
The subject is participating in an interventional study, a clinical trial, or a clinical investigation or is in a period of exclusion determined by a previous study
The subject refuses to sign the consent
It is impossible to give the subject informed information
The patient is under safeguard of justice or state guardianship
Trial design
Parallel
Treatments tested in this trial
Psilocybin (high dose)
Drug2 administrations of high-dose psilocybin (25 mg) 3 weeks apart
Psilocybin (low dose)
Drug2 administrations of low-dose psilocybin (3 mg) 3 weeks apart
Treatment groups
Trial outcomes
Primary outcomes
Incidence of relapse between groups
Relapse Yes/no, where relapse is defined as the 1st heavy drinking day, assessed using the Timeline Follow-Back (TLFB) method
Time to relapse between groups
Days until relapse, where relapse is defined as the 1st heavy drinking day, assessed using the Timeline Follow-Back (TLFB) method
Secondary outcomes
Change in relapse rate between groups
Assessed using the Timeline Follow-Back (TLFB) method
Change in rate of heavy drinking days between groups
Percent; Assessed using the Timeline Follow-Back (TLFB) method
Change in total alcohol consumption between groups
Grams, assessed using the Timeline Follow-Back (TLFB) method
Change in number of drinking days between groups
Days, assessed using the Timeline Follow-Back (TLFB) method
Sponsors and contacts
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