Evaluation of the peak experience scale as a rapid assessment tool for the strength of a psychoactive experience with 5-MeO-DMT.
Johannes T. Reckweg, Natasha L. Mason, Eef L. Theunissen, Claus B Svendsen, Theis H Terwey, Johannes G. Ramaekers
Frontiers in Psychology 2025 DOI: 10.3389/fpsyg.2025.1543640 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Sample size | 84 |
| Population | Healthy volunteers and patients with treatment resistant depression |
| Intervention | 5-MeO-DMT formulation (GH001) |
| Dose | 0 (placebo), 2, 6, 12, 18 mg or incremental individualized dosing regimen (IDR) |
| Topics | 5-MeO-DMT Mystical experience DMT |
| Keywords | Psychedelic Questionnaire Intensity Assess the strength Highly effective Strong correlation Ratings increased Rapidly assess Valuable Quick way Guide dosing Tool Simple Three-item 5-MEO-DMT: Mebufotenin Unique psychoactive compound Validated Understanding individual responses |
| Citations | 2 |
| Key findings | The three-item Peak Experience Scale is a valid and reliable tool for rapidly assessing the intensity of the 5-MeO-DMT psychedelic experience, showing strong correlation with established measures and dose-dependent increases in ratings. |
Abstract
A three-item Peak Experience Scale (PES) was developed to rapidly evaluate the strength of the psychoactive experience, and to guide the dosing regimen, of the psychedelic 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT; mebufotenin). This paper aims to compare the PES with a range of established questionnaires designed to evaluate the psychedelic experience. Data were gathered from three separate studies in which a 5-MeO-DMT formulation (GH001) was administered via pulmonary inhalation to healthy volunteers and patients with treatment resistant depression (N = 84) as either single doses (0 [placebo], 2, 6, 12, 18 mg) or an incremental individualized dosing regimen (IDR). Apart from the PES, participants also completed the Mystical Experience Questionnaire (MEQ-30), the Challenging Experience Questionnaire (CEQ), the Ego Dissolution Inventory (EDI) and the 5-Dimensional Altered States of Consciousness Rating Scale (5D-ASC). The 5-MeO-DMT formulation produced a significant, dose-related increase in PES ratings, with maximal ratings being achieved after the IDR. A principal component analysis (PCA) of the PES items identified a single primary component explaining 83.5% of the variance. PES items also displayed a strong internal consistency (Cronbach's α = 0.896). A PCA across all questionnaires indicated a strong and unidimensional loading of the PES, MEQ, EDI and the 5D-ASC, suggesting high interrelatedness. Likewise, individual ratings on the PES were highly correlated to those on the PES, MEQ, EDI and the 5D-ASC, but not the CEQ. The PES is concluded to be an effective tool to rapidly assess the strength of the psychedelic experience with 5-MeO-DMT. The PES could prove useful to gain fast insight into the strength of a psychedelic dose in individual patients and potentially guide dose and re-dose selection of rapid-acting psychedelics.
Comparable studies
Other observational and cohort studies on 5-MeO-DMT, most cited first.
Citations in the library
Cited by 3
- GH001 vs Placebo in Patients With Treatment-Resistant Depression JAMA Psychiatry March 25, 2026
- Exploratory Insights into 5-MeO-DMT Experiences on Reddit: A Thematic Analysis Journal of Psychoactive Drugs September 7, 2026
- Psychedelic Therapy: A Primer for Primary Care Clinicians—5-Methoxy-N,N-Dimethyltryptamine American Journal of Therapeutics February 20, 2026
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