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MDMA-assisted therapy: A new treatment model for social anxiety in autistic adults.

Alicia L Danforth, Christopher M Struble, Berra Yazar-Klosinski, Charles S Grob

Progress in neuro-psychopharmacology & biological psychiatry January 4, 2016 DOI: 10.1016/j.pnpbp.2015.03.011 via PubMed

Summary

AI-generated from the abstract

A clinical trial of MDMA-assisted therapy for social anxiety in autistic adults began in spring 2014. MDMA has been administered to over 1133 individuals in research without unexpected serious adverse events requiring expedited FDA reporting. The authors argue that established safety parameters justify developing MDMA-assisted interventions to help autistic adults improve social adaptability. MDMA, like classic psychedelics, can catalyze lasting openness and introspection without ongoing administration, reducing adverse event frequency and improving the risk/benefit ratio compared to daily medications. Clinicians could employ new treatment models using one to several MDMA sessions within supportive psychotherapy for social anxiety or similar distress.

Study at a glance

Characteristics Review Peer reviewed
Sample size 1,133
Population Individuals who have received MDMA for research purposes
Intervention MDMA-assisted therapy
Topics MDMA
Keywords Psychotherapy Social anxiety MDMA Therapy: MDMA Sessions
Citations 110
Key finding MDMA has been safely administered to over 1133 individuals in research, and its infrequent dosing may offer a favorable risk/benefit ratio for treating social anxiety in autistic adults.

Abstract

The first study of 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy for the treatment of social anxiety in autistic adults commenced in the spring of 2014. The search for psychotherapeutic options for autistic individuals is imperative considering the lack of effective conventional treatments for mental health diagnoses that are common in this population. Serious Adverse Events (SAEs) involving the administration of MDMA in clinical trials have been rare and non-life threatening. To date, MDMA has been administered to over 1133 individuals for research purposes without the occurrence of unexpected drug-related SAEs that require expedited reporting per FDA regulations. Now that safety parameters for limited use of MDMA in clinical settings have been established, a case can be made to further develop MDMA-assisted therapeutic interventions that could support autistic adults in increasing social adaptability among the typically developing population. As in the case with classic hallucinogens and other psychedelic drugs, MDMA catalyzes shifts toward openness and introspection that do not require ongoing administration to achieve lasting benefits. This infrequent dosing mitigates adverse event frequency and improves the risk/benefit ratio of MDMA, which may provide a significant advantage over medications that require daily dosing. Consequently, clinicians could employ new treatment models for social anxiety or similar types of distress administering MDMA on one to several occasions within the context of a supportive and integrative psychotherapy protocol.

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