Skip to content

Silence is golden: Documenting the speech production of participants and support providers in psilocybin administration sessions for the treatment of post-traumatic stress disorder

Robert F. Dougherty, Nadav Liam Modlin, Niall M. Mcgowan, Patrick Staples, Ella Williams, Patrick Clarke, Mario Shafiei, Carly Leininger, Merve Alti, Megan Croal, Lindsey Marwood, Namik Kirlic, Gregory Ryslik, Guy M. Goodwin

Journal of Psychopharmacology July 16, 2026 DOI: 10.1177/02698811261464988 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Peer reviewed
Sample size 22
Population Participants with post-traumatic stress disorder
Intervention COMP360 psilocybin
Dose 25 mg
Duration 12-week clinical trial
Topics Psilocybin PTSD
Keywords Context archaeology Thematic analysis Focus group Randomized controlled trial Silence Clinical psychology Psychotherapist Clinical trial
Registration NCT05312151
Key findings During psilocybin administration sessions, 78% of time was filled with silence, and support was minimally enacted but experientially salient.

Abstract

Background: When administered alongside monitoring and support, psilocybin has shown promise in the treatment of multiple psychiatric conditions. However, the contribution and nature of participant support in the context of psychedelic trials are much debated.

Aims: We sought to further illustrate the structure and format of the monitoring and support used in Compass Pathfinder Ltd (Compass) trials, with particular focus on the administration sessions.

Methods: Audio recording transcripts from a 12-week clinical trial evaluating the efficacy of 25 mg COMP360 psilocybin in 22 participants with post-traumatic stress disorder were analyzed to measure speech rates (words-per-minute (WPM)) for participants and support providers. A thematic analysis was also conducted on post-dosing participant interviews to offer further insight into how monitoring and support were experienced by participants.

Results: Comparison of support provider/participant WPM distinguished the administration from the preparation and follow-up sessions. Speech by either party during the administration sessions was rare; on average, 78% of the time was filled with silence, compared to 25% to 30% in non-administration sessions. Three main themes emerged in the thematic analysis: (1) support was minimally enacted, yet experientially salient, (2) autonomy was promoted through the introspective psychedelic state and non-directive support, and (3) primary modes of support during altered states of consciousness included reassurance and validation.

Conclusions: The relative absence of verbal interaction suggests that the monitoring and support used in Compass administration sessions can be differentiated from practice in many conventional psychotherapies, 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy trials, and psycholytic treatment paradigms with psychedelic drugs. ClinicalTrials.gov Identifier: NCT05312151 ( https://clinicaltrials.gov/study/NCT05312151 ).

In the evidence

This study is part of the evidence base for 2 syntheses in the library. Here is how each one recorded it.

  • Analyzed speech during 25 mg COMP360 psilocybin sessions, finding 78% of time was silence and support was minimally enacted yet experientially salient.

    Synthesized

  • During psilocybin administration sessions, 78% of time was filled with silence, and support was minimally enacted but experientially salient.

    Synthesized

Comparable studies

Other randomized controlled trials on PTSD, most cited first.

Study Year Design Participants
MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study. Patients with severe PTSD, including those with comorbidities such as dissociation,... 2021 Randomized controlled trial n = 90
The safety and efficacy of {+/-}3,4-methylenedioxymethamphetamine-assisted psychotherapy in subjects with chronic, treatment-resistant posttraumatic stress disorder: the first randomized controlled pilot study. Patients with chronic post-traumatic stress disorder refractory to both psychotherapy... 2010 Randomized controlled trial n = 20
Efficacy of Intravenous Ketamine for Treatment of Chronic Posttraumatic Stress Disorder Patients with chronic PTSD related to a range of trauma exposures 2014 Randomized controlled trial n = 41
3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for post-traumatic stress disorder in military veterans, firefighters, and police officers: a randomised, double-blind, dose-response, phase 2 clinical trial. Military veterans and first responders aged 18 or older with chronic PTSD lasting 6... 2018 Randomized, double-blind, dose-response, phase 2 clinical trial n = 26
A randomized, controlled pilot study of MDMA (±3,4-Methylenedioxymethamphetamine)-assisted psychotherapy for treatment of resistant, chronic Post-Traumatic Stress Disorder (PTSD) Patients with treatment-resistant PTSD 2012 Randomized controlled trial n = 12

Explore topics

By condition and practice