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Posttraumatic Growth After MDMA‐Assisted Psychotherapy for Posttraumatic Stress Disorder

Ingmar Gorman, Alexander Belser, Lisa Jerome, Colin Hennigan, Ben Shechet, Scott Hamilton, Berra Yazar-Klosinski, Amy Emerson, Allison A. Feduccia

Journal of Traumatic Stress February 19, 2020 Expression of concern DOI: 10.1002/jts.22479 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Pooled analysis of three phase 2 clinical trials with triple-blind crossover designs Peer reviewed
Sample size 60
Population Adults meeting DSM-IV-R criteria for PTSD with CAPS-IV score above 50 and prior inadequate response to treatment
Dose 75-125 mg MDMA (active); 0-40 mg MDMA (control)
Duration Primary endpoint (timing not specified), treatment exit, and 12-month follow-up
Measures Posttraumatic Growth Inventory (PTGI), Clinician-Administered PTSD Scale (CAPS-IV)
Topics MDMA Psychedelic-assisted therapy
Keywords Placebo Posttraumatic stress Posttraumatic growth Clinical endpoint Clinical trial Clinical psychology
Citations 43
Post-publication review 1 comment on PubPeer (opens in new tab) · last active August 2021
Key findings MDMA-assisted psychotherapy produced large-magnitude increases in posttraumatic growth and reductions in PTSD symptom severity, with two-thirds of participants no longer meeting PTSD criteria at 12-month follow-up.

Abstract

Abstract 3,4‐Methylenedioxymethamphetamine (MDMA)–assisted psychotherapy for posttraumatic stress disorder (PTSD) has been shown to significantly reduce clinical symptomatology, but posttraumatic growth (PTG), which consists of positive changes in self‐perception, interpersonal relationships, or philosophy of life, has not been studied with this treatment. Participant data ( n = 60) were pooled from three Phase 2 clinical studies employing triple‐blind crossover designs. Participants were required to meet DSM‐IV‐R criteria for PTSD with a score higher than 50 on the Clinician‐Administered PTSD Scale (CAPS‐IV) as well as previous inadequate response to pharmacological and/or psychotherapeutic treatment. Data were aggregated into two groups: an active MDMA dose group (75–125 mg of MDMA; n = 45) or placebo/active control (0–40 mg of MDMA; n = 15). Measures included the Posttraumatic Growth Inventory (PTGI) and the CAPS‐IV, which were administered at baseline, primary endpoint, treatment exit, and 12‐month follow‐up. At primary endpoint, the MDMA group demonstrated more PTG, Hedges’ g = 1.14, 95% CI [0.49, 1.78], p < .001; and a larger reduction in PTSD symptom severity, Hedges’ g = 0.88, 95% CI [−0.28, 1.50], p < .001, relative to the control group. Relative to baseline, at the 12‐month follow‐up, within‐subject PTG was higher, p < .001; PTSD symptom severity scores were lower, p < .001; and two‐thirds of participants (67.2%) no longer met criteria for PTSD. MDMA‐assisted psychotherapy for PTSD resulted in PTG and clinical symptom reductions of large‐magnitude effect sizes. Results suggest that PTG may provide a new mechanism of action warranting further study.

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