Behavioral Pharmacology Research Unit, Johns Hopkins Bayview Medical Center
Baltimore, Maryland, 21224, United States
NCT Number: NCT02971605
The proposed pilot study will assess whether ingestion of a classic hallucinogen (psilocybin) leads to changes in emotion processing and neural circuitry that may predict repeated self-administration of this drug and underlie an atypical mechanism of abuse liability, which may vitally contribute to the understanding of the potential for abuse and the underlying mechanisms supporting abuse of classic hallucinogens.
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Notify Me18 year–45 year
All sexes
Interventional
Phase 1 / Phase 2
Baltimore, Maryland, 21224, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
25 mg/70 kg Psilocybin
Time frame: 1 day pre (baseline), 1 week post, and 1 month post session
Blood oxygenation level-dependent (BOLD) percent signal change in response to stimuli in the emotion recognition task was measured in the left and right amygdala.
Time frame: 1 day pre (baseline), 1 week post, and 1 month post session
Participants were assessed on a variety of questionnaires that probed emotional functioning and mood state. Higher scores on each subscale are indicative of higher levels of each emotion/mood (e.g., low score on Depression (POMS) indicates low level of depressed mood).
Depression Anxiety Stress Scale (DASS): Range 0-56 on all subscales
Dispositional Positive Emotion Scale (DPES): Range 1-7 on all subscales
Positive & Negative Affect Schedule Expanded (PANAS-X): Range 0-50 on all subscales
Profile of Mood States (POMS): Ranges vary by subscale. Tension (0-36); Depression (0-60); Anger (0-48); Fatigue (0-28); Confusion (0-28); Vigor (0-36); Mood Disturbance (-36-168)
State Trait Anxiety Inventory (STAI): Range 20-80 on all subscales
Tellegen Absorption Scale (TAS): Range 0-34
Big Five Inventory (BFI): Range 1-5 on all subscales
Time frame: 1 day pre (baseline), 1 week post, and 1 month post session
These tasks measure emotional responding that may be altered by psilocybin.
Emotional discrimination task: participants were presented with images of emotional facial expressions or shapes (control), and were instructed to discriminate between the images.
Emotion recognition task: participants were presented images of actors and were asked to identify the emotional facial expression (happy, sad, fear, angry, neutral) of each actor.
Emotional conflict Stroop task: participants were shown emotional facial expressions (targets) with emotional words overlain (distractors) and were asked to identify the valence of the facial expression, either positive or negative.
Time frame: 1-day pre (baseline), 1-week post, 1-month post session
These tasks measure emotional responding that may be altered by psilocybin.
Emotional discrimination task: participants were presented with images of emotional facial expressions or shapes (control), and were instructed to discriminate between the images.
Emotion recognition task: participants were presented images of actors and were asked to identify the emotional facial expression (happy, sad, fear, angry, neutral) of each actor.
Emotional conflict Stroop task: participants were shown emotional facial expressions (targets) with emotional words overlain (distractors) and were asked to identify the valence of the facial expression, either positive or negative.
Johns Hopkins University
Other
Measurement of Persisting Changes in Emotional Brain Functioning Produced by Psilocybin
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