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Psilocybin microdosing does not affect emotion-related symptoms and processing: A preregistered field and lab-based
Josephine Marschall1, George Fejer1, Pascal Lempe1
1Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Journal of Psychopharmacology (Oxford, England)
|December 17, 2021
Summary
Psilocybin microdosing did not significantly alter emotion processing or reduce anxiety and depression symptoms in this study. Further research is needed to confirm potential benefits in a clinical population.
Area of Science:
- Neuroscience
- Psychopharmacology
- Clinical Psychology
Background:
- Anecdotal reports suggest microdoses of psychedelics can alleviate depression, anxiety, and stress.
- Psilocybin research at higher doses indicates potential mechanisms involving emotion and interoceptive processing modulation.
Purpose of the Study:
- To investigate if psilocybin microdoses affect self-reported interoceptive awareness.
- To determine if repeated microdosing over three weeks modulates emotion processing and reduces anxiety and depression symptoms.
Main Methods:
- A double-blind, placebo-controlled, within-subject crossover design was employed.
- Participants self-administered psilocybin microdoses or placebo every third day for three weeks.
- Assessments included the Multidimensional Assessment of Interoceptive Awareness Questionnaire, emotional go/no-go task, and Depression Anxiety Stress Scale.
Main Results:
- Confirmatory analyses showed no significant effect of psilocybin microdosing on emotion processing or anxiety and depression symptoms compared to placebo.
- Exploratory analyses indicated no impact on self-reported interoceptive awareness.
- While depression and stress symptoms reduced in the first block, participants broke blind in the second block, and expectations had no effect.
Conclusions:
- Psilocybin microdosing did not demonstrate efficacy in this study for improving emotion processing or reducing anxiety and depression symptoms.
- Further investigation in a substance-naïve population with clinical anxiety and depressive symptoms is warranted to validate potential benefits.
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