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Emily C. Fewster

York University

3 papers in the library · 23 citations · publishing 2024-2025

Papers

Keeping the promise: a critique of the current state of microdosing research

Frontiers in Psychiatry February 5, 2024 Rotem Petranker, Thomas Anderson, Youval Aberman et al. 14 citations

Microdosing, the practice of taking small, sub-hallucinogenic doses of psychedelics, has become popular, with users reporting benefits like improved mood and creativity. A review of 15 papers published before March 2022 critically analyzed the research practices in this field. The review concludes that it is premature to draw any conclusions about the efficacy or safety of microdosing because the quality of the research is not confirmatory. The authors propose potential causes for this state of the literature and offer suggestions for improvement.

Global Trends in Psychedelic Microdosing: Demographics, Substance Testing Behavior, and Patterns of Use

Journal of Psychoactive Drugs November 6, 2024 Rotem Petranker, Valentyn Sobolenko, Zeina Beidas et al. 9 citations

People who exclusively microdose psychedelics differ from those who also take larger doses. Exclusive microdosers are older (average 46.4 vs. 42.0 years), more often female (68.4% vs. 44.7%), non-Caucasian (25.4% vs. 14.7%), and urban residents (43.9% vs. 38.5%). They report using fewer non-psychedelic substances over their lifetime (3.8 vs. 4.7 substances). Most microdose multiple times a month (52.5%), commonly using psilocybin (74.5%), LSD (34.4%), or ketamine (15.8%), and 64.6% do not test their substances. The main reason for microdosing is improving general wellbeing (73.0%).

Microdosing Psilocybin for Major Depressive Disorder: Study Protocol for a Phase II Double-Blind Placebo-Controlled Randomized Partial Crossover Trial

November 16, 2025 Zeina Beidas, Anya Ragnhildstveit, Adam Blackman et al. preprint

A phase II trial will test whether microdosing psilocybin (2 mg weekly) outperforms placebo for major depressive disorder. Forty adults will receive either psilocybin or placebo for four weeks, then all will receive psilocybin for another four weeks. Depression symptoms and other measures will be assessed at baseline, after four weeks, and after eight weeks, with follow-ups for two years. The study aims to clarify whether microdosing has genuine antidepressant effects or whether benefits are due to expectancy, and to inform future dose regimens and the therapeutic role of sub-threshold versus threshold doses.