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B-56Investigation of Personality Change Following MDMA-Assisted Psychotherapy for Post Traumatic Stress Disorder

Michael Wagner, Michael C Mithoefer, Ann T Mithoefer, Rebecca K. MacAulay, Lisa Jerome, B Bazaar-Klosinski, Rick Doblin

Archives of Clinical Neuropsychology August 31, 2016 DOI: 10.1093/arclin/acw043.131 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Peer reviewed
Sample size 20
Population Subjects with treatment-refractory PTSD
Intervention MDMA-assisted psychotherapy
Dose 125 mg
Topics MDMA PTSD Psychedelic-assisted therapy
Keywords Psychotherapist Clinical psychology Borderline personality disorder
Citations 1
Key findings Increases in Openness and decreases in Neuroticism predicted lower PTSD severity, with MDMA-treated participants showing the greatest increase in Openness.

Abstract

Objective: New data from a previously published randomized blinded Phase II clinical trial (Mithoefer, et al., 2011) is presented here to test whether psychological change mediates the effect of 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for chronic, treatment-resistant PTSD.

Method: Twenty-three (23) subjects with treatment-refractory PTSD were randomized to either a placebo or experimental condition. Subjects received 2-3 experimental sessions of 125 mg MDMA-assisted psychotherapy (N = 12) or inactive placebo and psychotherapy (N = 8) according to FDA/IRB approved protocol. The CAPS and NEO PI-R were primary outcome measures.

Results: There was a significant main effect of decreased CAPS scores, independent of treatment condition when Openness F(1, 17) = 40.60 p < .001 or Neuroticism F(1, 17) = 20.48, p < .001 were used as covariates. Significant interactions showed that experimental subjects experienced the greatest increase in Openness, concomitantly demonstrating greater decreases in CAPS score, F(1, 17) = 5.68, p = .029; also decreases in Neuroticism were associated with a decreased CAPS score, F(1, 17) = 18.83, p < .001. Change score of increased Openness predicted a lower CAPS score, r = .525, p = .031; while decreases in Neuroticism predicted lower CAPS score, r = .492, p = .028.

Conclusion: Psychological learning models do not seem to fit these data. With psychotherapeutic priming and MDMA, resolution of PTSD with associated change in personality trait, was conceptualized as involving a transient alteration in the temporal/cingulate, amygdala, and ventromedial frontal pathways of the brain resulting in an “aha” type reorganization of mental experience.

Comparable studies

Other randomized controlled trials on MDMA and psychedelic-assisted therapy, most cited first.

Study Year Design Participants
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
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
Reduction in social anxiety after MDMA-assisted psychotherapy with autistic adults: a randomized, double-blind, placebo-controlled pilot study. Autistic adults with marked to very severe social anxiety 2018 Randomized controlled trial n = 12
3,4-Methylenedioxymethamphetamine-assisted psychotherapy for treatment of chronic posttraumatic stress disorder: A randomized phase 2 controlled trial. People with chronic posttraumatic stress disorder 2018 Randomized controlled trial n = 28

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