This study aims to study the feasibility of psilocybin therapy for patients with Amyotropic Lateral Sclerosis (ALS) with depressed mood. The secondary objective is to assess its impact on depression, quality of life, hopelessness, and functional status in this patient population.
The proposed research's primary objective is to study the feasibility of psilocybin therapy for patients with ALS with depressed mood. The secondary objective is to assess its impact on depression, quality of life, hopelessness, and functional status in this patient population. The proposed proof-of-concept interventional trial will use a single-arm design. The study will be an open-label trial in a sample of up to 24 treatment-seeking patients with a diagnosis of ALS and depressed mood. Participants will complete an 8-week course of study treatment including two psilocybin sessions (15 mg in week 4 and 15 or 25 mg in week 6), with follow-up assessments 1, 3, and 6 months after the final psilocybin session.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Psilocybin Trihydrate. Participants will complete an 8-week course of study treatment including two psilocybin sessions (15 mg in week 4 and 15 or 25 mg in week 6), with follow-up assessments 1, 3, and 6 months after the final psilocybin session.
Johns Hopkins Center for Psychedelic and Consciousness Research
Baltimore, Maryland, United States
RECRUITINGFeasibility of psilocybin treatment as assessed by number of participants recruited, retained and adhere to treatment
feasibility will be assessed by participant recruitment, retention, and treatment adherence.
Time frame: 6 months
Depressive symptoms as assessed by the Montgomery-Asberg Depression Rating Scale
Depressive symptoms from baseline at 1 week and 1 month after final psilocybin session measured by the Montgomery-Asberg Depression Rating Scale. Score range: 0-60; higher scores = worse outcome
Time frame: Baseline, 1 week post psilocybin session, 1 month post psilocybin session
Depressive symptoms as assessed by the and ALS Depression Inventory
Depressive symptoms from baseline at 1 week and 1 month after final psilocybin session measured by the ALS Depression Inventory. Score ranges from 12 (best) to 48 (worst), with scores between 23 and 29 indicating mild depression and scores above 30 indicating severe depression.
Time frame: Baseline, 1 week post psilocybin session, 1 month post psilocybin session
Impact of psilocybin treatment on quality of life as assessed by the EuroQoL 5-dimension, 3-level (EQ-5D-3L) 5-item ALS Assessment Questionnaire
Impact on quality of life measured by the 5-dimension, 3-level EuroQol, 5-item ALS Assessment Questionnaire. Score range 5-25; higher score more problems. The EQ-5D-3L also includes an EQ VAS, which is a vertical scale where respondents rate their health from "the best health you can imagine" to "the worst health you can imagine". The EQ-5D-3L index is calculated by subtracting the descriptive system values from 1, with 1 representing the best possible health status and a value below 0 representing the worst.
Time frame: 6 months
Impact of psilocybin treatment on hopelessness as assessed by the Beck Hopelessness Scale
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Impact on hopelessness measured by the Beck Hopelessness Scale. Scores range from 0-20 with higher scores indicating a greater degree of hopelessness.
Time frame: 6 months
Impact of psilocybin treatment on function as assessed by the ALS Functional Rating Scale-Revised
Impact of function measured by the ALS Functional Rating Scale-Revised. Scale from 0 = can't do, to 4 = normal ability, with a total score range of 0- 52 points. Higher score better outcome.
Time frame: 6 months