A comparison of MDMA-assisted psychotherapy to non-assisted psychotherapy in treatment-resistant PTSD: A systematic review and meta-analysis.
Study Goal
The researchers aimed to evaluate the therapeutic benefits and safety of MDMA-assisted psychotherapy for treatment-resistant PTSD.
Results Summary
MDMA-assisted psychotherapy significantly reduced PTSD symptoms (CAPS-IV scores) at 75 mg and 125 mg doses compared to placebo, with minimal physical and neurocognitive risks. However, effects on depression (BDI) were limited to the 75 mg dose, and some adverse effects like low mood, nausea, and jaw-clenching were reported.
Population
Individuals with treatment-resistant post-traumatic stress disorder (PTSD).
Effective Dosage
75 mg, 100 mg, and 125 mg of MDMA with psychotherapy.
Duration
Not specified in the abstract.
Interactions
None mentioned.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
MDMA-assisted psychotherapy | decrease | CAPS-IV scores | treatment-resistant PTSD | MD -46.90; 95% CI -58.78, -35.02 | had significant decreases | #1 |
MDMA-assisted psychotherapy | decrease | CAPS-IV scores | treatment-resistant PTSD | MD -20.98; 95% CI -34.35, -7.61 | had significant decreases | #2 |
MDMA-assisted psychotherapy | decrease | CAPS-IV scores | treatment-resistant PTSD | MD -33.20; 95% CI -40.53, -25.87 | had significant decreases | #3 |
MDMA-assisted psychotherapy | decrease | BDI | treatment-resistant PTSD | MD -10.80; 95% CI -20.39, -1.21 | A significant decrease | #4 |
MDMA-assisted psychotherapy | increase | low mood | participants | - | reported significantly more episodes | #5 |
MDMA-assisted psychotherapy | increase | nausea | participants | - | reported significantly more episodes | #6 |
MDMA-assisted psychotherapy | increase | jaw-clenching | participants | - | reported significantly more episodes | #7 |
MDMA-assisted psychotherapy | increase | lack of appetite | participants | - | reported significantly more episodes | #8 |
MDMA-assisted psychotherapy | no change | Beck's Depression Inventory | treatment-resistant PTSD | - | little effect | #9 |
RATIONALE: Novel, evidence-based treatments are required for treatment-resistant post-traumatic stress disorder (PTSD). 3,4-Methylenedioxymethamphetamine (MDMA) has beneficially augmented psychotherapy in several small clinical trials. OBJECTIVE: To review the use of MDMA-assisted psychotherapy in treatment-resistant PTSD. METHODS: Systematic searches of four databases were conducted from inception to February 2020. A meta-analysis was performed on trials which were double-blinded, randomised, and compared MDMA-assisted psychotherapy to psychotherapy and placebo. The primary outcomes were the differences in Clinician Administered PTSD Scale (CAPS-IV) score and Beck's Depression Inventory (BDI). Secondary outcome measures included neurocognitive and physical adverse effects, at the time, and within 7 days of intervention. RESULTS: Four randomised controlled trials (RCTs) met inclusion criteria. When compared to active placebo, intervention groups taking 75 mg (MD -46.90; 95% (confidence intervals) CI -58.78, -35.02), 125 mg (MD -20.98; 95% CI -34.35, -7.61) but not 100 mg (MD -12.90; 95% CI -36.09, 10.29) of MDMA with psychotherapy, had significant decreases in CAPS-IV scores, as did the inactive placebo arm (MD -33.20; 95% CI -40.53, -25.87). A significant decrease in BDI when compared to active placebo (MD -10.80; 95% CI -20.39, -1.21) was only observed at 75 mg. Compared to placebo, participants reported significantly more episodes of low mood, nausea and jaw-clenching during sessions and lack of appetite after 7 days. CONCLUSION: These results demonstrate potential therapeutic benefit with minimal physical and neurocognitive risk for the use of MDMA-assisted psychotherapy in TR-PTSD, despite little effect on Beck's Depression Inventory. Better powered RCTs are required to investigate further. INTERNATIONAL PROSPECTIVE REGISTER OF SYSTEMATIC REVIEWS: CRD42019109132 available online at www.crd.york.ac.uk/prospero.