RETRACTED ARTICLE: Long-term follow-up outcomes of MDMA-assisted psychotherapy for treatment of PTSD: a longitudinal pooled analysis of six phase 2 trials
Lisa Jerome, Allison A. Feduccia, Julie B. Wang, Scott Hamilton, Berra Yazar‐Klosinski, Amy Emerson et al. · 2020 · 164 citationsRead the paper
RATIONALE: Posttraumatic stress disorder (PTSD) is a chronic condition that has wide-ranging negative effects on an individual's health and interpersonal relationships. Treatments with long-term benefits are needed to promote the safety and well-being of those suffering from PTSD. OBJECTIVES: To examine long-term change in PTSD symptoms and additional benefits/harms after 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for treatment of PTSD. METHODS: Participants received two to three active doses of MDMA (75-125 mg) during blinded or open-label psychotherapy sessions with additional non-drug therapy sessions. PTSD symptoms were assessed using the Clinician-Administered PTSD Scale for DSM IV (CAPS-IV) at baseline, 1 to 2 months after the last active MDMA session (treatment exit), and at least 12 months post final MDMA session (LTFU). A mixed-effect repeated-measures (MMRM) analysis assessed changes in CAPS-IV total severity scores. The number of participants who met PTSD diagnostic criteria was summarized at each time point. Participants completed a long-term follow-up questionnaire. RESULTS: There was a significant reduction in CAPS-IV total severity scores from baseline to treatment exit (LS mean (SE) = - 44.8 (2.82), p < .0001), with a Cohen's d effect size of 1.58 (95% CI = 1.24, 1.91). CAPS-IV scores continued to decrease from treatment exit to LTFU (LS mean (SE) = - 5.2 (2.29), p < .05), with a Cohen's d effect size of 0.23 (95% CI = 0.04, 0.43). The number of participants who no longer met PTSD criteria increased from treatment exit (56.0%) to LTFU (67.0%). The majority of participants reported benefits, including improved relationships and well-being, and a minority reported harms from study participation. CONCLUSIONS: PTSD symptoms were reduced 1 to 2 months after MDMA-assisted psychotherapy, and symptom improvement continued at least 12 months post-treatment. Phase 3 trials are investigating this novel treatment approach in a larger sample of participants with chronic PTSD. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00090064, NCT00353938, NCT01958593, NCT01211405, NCT01689740, NCT01793610.
What the full text shows
Working prototype- Significant reduction in PTSD symptom severity from baseline to treatment exit. — LS mean = -44.8 (SE 2.82), Cohen's d = 1.58 (100 participants receiving 2-3 active doses of MDMA (75-125 mg) and psychotherapy)
- Further reduction in PTSD symptom severity from treatment exit to long-term follow-up. — LS mean = -5.2 (SE 2.29), Cohen's d = 0.23 (Long-term follow-up at least 12 months post-treatment)
- Increase in the proportion of participants no longer meeting PTSD diagnostic criteria. — 56.0% at treatment exit to 67.0% at long-term follow-up (Pooled analysis of six phase 2 trials)
- Reduction in positive suicidal ideation. — 60.3% at baseline to 24.2% at long-term follow-up (Subset of 68 participants administered the C-SSRS)
- High rate of perceived treatment benefits. — 97.6% reported benefits; 53.2% indicated large benefits that lasted or grew (Self-reported via LTFUQ at 12-month follow-up)
- Low treatment dropout rate. — 7.6% dropout rate (Across six phase 2 studies during the treatment period)
- Setup
- 107 participants with moderate to severe chronic PTSD; 91 completed CAPS-IV long-term follow-up; 83 completed the LTFUQ.
- How
- Pooled analysis of six phase 2 trials where participants received 2-3 active doses of MDMA (75-125 mg) during psychotherapy sessions. Outcomes were measured using the CAPS-IV scale at baseline, treatment exit (1-2 months post-treatment), and long-term follow-up (12+ months).
- Limitations
- Lack of a long-term control group (all participants received active MDMA by LTFU), limiting causality conclusions. · Small sample size for harm analysis (only 7 participants reported harms). · Pooled analysis of studies with some variations in design and timing.
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