Redefining the real problem in psychedelic trials: Why fighting the Lessebo matters more than blinding integrity.
Laetitia Vanderijst, Jean-luc Faillie, Thibault Mura, Amandine Luquiens
The International journal on drug policy July 8, 2026 Peer reviewed DOI: 10.1016/j.drugpo.2026.105423 via PubMed
Summary
Imperfect blinding is common in trials, particularly in psychedelics, where treatment allocation is often guessed. This issue is not typically addressed in mental health research, leading to biases against patient-reported outcomes. The concept of 'lessebo,' a negative placebo effect from disappointment, highlights the need for better management of expectations rather than striving for perfect blinding. Strategies like structured psychoeducation could improve trial outcomes and ethical standards.
Study at a glance
| Key finding | The study emphasizes managing disappointment over achieving perfect blinding to mitigate negative placebo effects in psychedelic trials. |
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Abstract
Imperfect blinding is not specific to psychedelic trials. In randomized trials, treatment allocation is frequently correctly guessed, yet blinding integrity is rarely assessed outside of psychedelic research and is generally not considered a barrier in regulatory evaluation. The intense debate in psychedelics may reflect a broader double standard affecting mental health research, when uncertainties arising from imperfect blinding are confounded by those linked to patient-reported outcome measures. Indeed, people living with mental disorders are often viewed as unreliable reporters, despite well-documented limitations of clinician-rated scales and the absence of robust biological markers of symptomatic change. Importantly, it is the maintenance of reasonable doubt of treatment allocation that sustains internal validity and ethical feasibility of placebo-controlled designs, rather than perfect blinding. Concerns about expectancy bias in psychedelic trials are closely tied to blinding debates. When allocation is inferred, expectations may cluster in the arm perceived as active or in stereotyped experiences and influence outcomes differently in active and control arms, leading to a risk of lessebo, a negative placebo effect due to the negative expectation related to receiving a placebo. However, we argue that an underrecognized mechanism of lessebo is disappointment. This risk may reflect insufficient clinical management of disappointment rather than pre-treatment expectation alone. We therefore propose shifting the emphasis from preserving inevitably imperfect blinding towards mitigating disappointment in both arms. Establishing non-stereotyped expectations prior to treatment through structured psychoeducation, strengthened therapeutic alliance, and realistic preparation would help avoid lessebo effects. Such strategies would enhance ethical rigor, interpretability, and the clinical usefulness of psychedelic trials.