Recruiting · registry statusPsilocybin therapy for depression during serious illness
Researchers are studying psilocybin with psychological support for depression in people with several serious conditions, including atypical Parkinson's.
Testing a treatment or activity · Study reference: NCT06782724
Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓
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Looking for volunteers
- Start (planned)
- 2025-01-01
- Study finished (planned)
- 2027-01-01
Planned dates can move. A study finishing does not tell us when a paper will be published.
No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.
Changes we have recorded
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Papers connected to this study
No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.
Who can join?
Age range not listed · Ask the team who can join
These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.
Read all the rules for taking part
Sex eligibility reported by registry: Not reported
COPD: diagnosis by specialist
APD: Diseases in the spectrum of Progressive supranuclear palsy (PSP), fulfilling possible and probable criteria, according to the MDS diagnostic criteria
APD: Clinically Established and Clinically Probable Multiple System Atrophy (MSA) according to the MDS diagnostic criteria
Patient meets ICD-10 criteria for major depressive disorder documented through the completion of the mood section of the Mini International Neuropsychiatric Interview by a screening psychologist or physician
Patient has a MADRS score of > 19
Patient should have a life expectancy of at least 6 months (assessed by study physician)
Patient is at least 18 years of age
Patient has an identified caregiver/support person
Patient is able to read and understand the informed consent and all scales used in a local language. For those with ALS, MS, or APD, competency is ensured via neurologist assessment, cognitive screening, caregiver support during screening and interactive approaches where the screening clinician ask the patient to explain their understanding of consent elements, re-explaining potentially misunderstood information
Patient is able to and willing to adhere to study requirements, including attending all study visits, preparatory and follow-up sessions, and completing all study evaluations
Patient is able to ingest capsules
COPD: Postbronchodilator FEV1/FVC < 0,7 and FEV1 <80% pred
COPD: ≥ 40 years old
COPD: ≥ 10 years smoking
ALS: ALS according to Goldcoast criteria
ALS: ALS-FRS-R subscores of minimum 1 in item 2, 3 and 8, subscore of minimum 2 in item 1, 4 and 10 and a subscore of minimum 3 in item 11 and 12
MS: Fulfilled diagnostic revised McDonald criteria for MS from 2017
MS: EDSS ≥ 1,0
APD: Advanced to Late-Stage Parkinson’s Disease – patients with a diagnosis of Parkinson’s Disease per the MDS clinical diagnosis criteria with evidence of motor and non-motor fluctuations
Patient has used a psychedelic substance in the past 6 months (e.g., psilocybin, LSD, 5-MeO-DMT, DMT, ayahuasca or mescaline)
Patient is unwilling or unable to pause formal psychotherapy (days 0-42)
Patient has neurological conditions (e.g., intracranial tumour, epilepsy, brain injuries, or other neurological disorders) expected by the PIs to conflict with the treatment / study protocol
Cardiovascular conditions: recent stroke ( 140/90 mmHg), clinically significant arrhythmia within 1 year of signing the ICF, or QTc prolongation exceeding 450ms (males) / 470ms (females).
Patient has moderate to severe hepatic impairment (Child-Pugh score ≥ 7)
Patient has insulin-dependent diabetes or who are taking oral hypoglycaemic agents and have a current risk of hypoglycaemia that would require medical intervention
Patient has any physical or psychological symptoms, medications, blood test results or clinically significant findings at Screening or Baseline (based on the clinical judgement of clinical/medical study personnel) that would make a patient unsuitable for the study
Patient has an allergy or intolerance to any of the materials contained in either drug product
Cognitive and Neuropsychological assessment: Patients will be excluded if they score below mean minus 1.5 Standard Deviation according to normative age and scholarity adjusted data on the Montreal Cognitive Assessment (MoCA) assessment
Recent (2 weeks) change or planned change in antidepressant medication during the intervention
Women who are pregnant, intend to become pregnant during the study, who are currently nursing or are unwilling to use Highly Effective Contraceptive Methods (section 8.2.1).
Patient is in active treatments for other psychiatric disorders, judged by the screening clinician to be a more significant clinical problem than depression / distress
COPD: Unresolved exacerbation or pulmonary infection within last 4 weeks
ALS: Significant cognitive deficits (MoCA)
MS: Significant cognitive deficits (MoCA), epilepsy or radiologically isolated syndrome
APD: Dementia (MoCa), or Schwab and England ADL scale with scores > 80% in the best functional state
Patient meets ICD-10 criteria for schizophrenia spectrum or other psychotic disorders, including major depressive disorder with psychotic features (except substance/medication-induced or due to another medical condition) or bipolar I/II disorder
Patients with any lifetime diagnosis of schizophrenia spectrum or other psychotic disorders
Patient has a first-degree relative with schizophrenia spectrum, bipolar I disorder or other psychotic disorders (expect substance/medication-induced or due to another medical condition).
Patients with a pre-existing psychiatric condition judged to be incompatible with safe exposure to psilocybin therapy
Significant suicide risk as defined by (1) suicidal ideation with intent to act (defined as ≥ 5 on MADRS item 10), (2) suicidal attempts within the past year, or (3) clinical assessment of significant suicidal risk during patient interview
Patient meets ICD-10 criteria for active/current alcohol or drug use disorder
Patient has ongoing treatment with antipsychotic drugs. Any prohibited agents must have been stopped at least 5x the elimination half-life of the specific drug at the time of baseline (see Appendix 1a of the Clinical Trial Protocol for Prohibited medications)
Full study name & original research details
Official study title
PsyPal; Psilocybin Therapy for Psychological Distress in Palliative Patients
Original description
To examine medium/high-dose psilocybin therapy safety and efficacy in reducing symptoms of depression in patients with COPD, ALS, MS, or APD, compared to the low-dose control group. This will be determined by using the clinician-administered Montgomery Åsberg Depression Rating Scale (MADRS) score and comparing changes between scores at Baseline and Primary endpoint (6 weeks post Dose 2).
Conditions reported: Chronic obstructive pulmonary disease (COPD), amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), and atypical Parkinson disorder (APD), particularly multiple system atrophy (MSA), progressive supranuclear palsy (PSP), and corticobasal syndrome (CBS).
Registry records for this study
Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.
- Study type
- Interventional
- Interventions
- Psilocybin capsules 15 mg, Psilocybin capsules 1 mg, Psilocybin capsules 25 mg
- Phases
- Therapeutic exploratory (Phase II)
- Sponsor
- Universitair Medisch Centrum Groningen
- Start date reported by registry
- 2025-01-01 (estimated)
Registry updated: 2026-09-22 · Status last verified by the registry submitter: Not reported
Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.
Contact the research team
Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.
Prof. Dr. Robert Schoevers · +31503616161 · r.a.schoevers@umcg
Study locations
Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.
National Institute of Mental Health
Prague, Czechia
RecruitingTomas Palenicek · tomas.palenicek@nudz.cz
Tomas Palenicek
Bispebjerg Hospital
Copenhagen, Denmark
RecruitingKirsten Svenstrup · kirsten.svenstrup@regionh.dk
Kirsten Svenstrup
Dea Siggaard Stenbaek
University Medical Center Groningen
Groningen, Provincie Groningen, Netherlands
RecruitingRobert Schoevers · r.a.schoevers@umcg.nl
Sanne Smith-Apeldoorn
Jeanine Kamphuis
Champalimaud Foundation
Lisbon, Portugal
RecruitingAlbino Oliveira-Maia · albino.maia@neuro.fchampalimaud.org
Albino Oliveira-Maia
Carolina Seybert
Facility not reported
Denmark
Status not reportedFacility not reported
Czechia
Status not reportedFacility not reported
Portugal
Status not reportedFacility not reported
Netherlands
Status not reportedRegion Hovedstaden
Copenhagen Nv, Denmark
Not yet recruitingNarodni Ustav Dusevniho Zdravi
Klecany, Czechia
RecruitingChampalimaud Clinical Centre
Lisbon, Portugal
RecruitingUniversitair Medisch Centrum Groningen
Groningen, Netherlands
RecruitingThe original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.