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Debunking the myth of 'Blue Mondays': No evidence of affect drop after taking clinical MDMA.

Ben Sessa, Jacob S. Aday, Steve O’Brien, Helen Valerie Curran, Fiona Measham, Laurie Higbed, David Nutt

Journal of Psychopharmacology December 13, 2021 DOI: 10.1177/02698811211055809 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Open-label study Peer reviewed
Sample size 14
Population Participants receiving clinically administered MDMA
Interventions 3 4-methylenedioxymethamphetamine (MDMA) as an adjunct to psychotherapy
Duration 1-week post-administration follow-up for mood; 3- and 6-month follow-ups for sleep quality
Topics MDMA
Keywords 3 4-methylenedioxymethamphetamine Emotional state Affect Well-being Positive feelings Negative feelings Clinical research Controlled administration Clinical contexts Scientific investigation Controlled trial After-effects Post-experience dip Post-MDMA Effects "blue monday" crash Mood drop Aftermath
Citations 18
Key points Participants maintained a positive mood during the week following clinical MDMA administration, with no reported illicit use or desire for it.

Abstract

Background: Incorporating 3,4-methylenedioxymethamphetamine (MDMA) as an adjunct to psychotherapy has shown promise in recent years for treating various mental health conditions, particularly those involving trauma. However, concerns about declines in mood and cognition during the days following dosing, also known as 'Blue Mondays', have been raised as limitations to its clinical use. Although these changes have been well-documented among recreational users, there are critical confounds to these reports that limit generalizability to clinically administered MDMA.

Aims: Here, we aimed to evaluate the evidence basis for the negative side effects associated with MDMA as well as inform our understanding of the drug's post-acute effects in a clinical context with an open-label study.

Methods: = 14) and measured mood, sleep quality, illicit MDMA consumption and anecdotal reports after the acute drug effects had worn off.

Results: Participants maintained a positive mood during the week following drug administration in a clinical context. Relative to baseline, self-reported sleep quality improved at the 3- and 6-month follow-ups. Finally, no participants reported using or desiring to use illicit MDMA, and the anecdotal reports indicated that they perceived the treatment favourably.

Conclusion: The results support the overall safety and tolerability of clinically administered MDMA and, importantly, suggest that the 'come downs' previously associated with the substance may be explained by confounds in research relating to the illicit sourcing of the drug and specific environmental setting for recreational consumption.

Comparable studies

Other non-randomized and open-label trials on MDMA, most cited first.

Study Year Design Participants
Durability of improvement in post-traumatic stress disorder symptoms and absence of harmful effects or drug dependency after 3,4-methylenedioxymethamphetamine-assisted psychotherapy: a prospective long-term follow-up study. Adults with chronic, treatment-resistant PTSD 2013 Long-term follow-up of a completed trial n = 19
First study of safety and tolerability of 3,4-methylenedioxymethamphetamine-assisted psychotherapy in patients with alcohol use disorder. Patients with alcohol use disorder (AUD) following community alcohol detoxification 2021 Open-label safety and tolerability proof-of-concept study n = 14
MDMA-facilitated cognitive-behavioural conjoint therapy for posttraumatic stress disorder: an uncontrolled trial. Couples in which one partner was diagnosed with PTSD 2020 Pilot study n = 6
Culturally informed research design issues in a study for MDMA-assisted psychotherapy for posttraumatic stress disorder People of color with posttraumatic stress disorder 2019 Phase 2 open-label multisite study
The Consequences of 3,4-Methylenedioxymethamphetamine Induced CYP2D6 Inhibition in Humans Healthy male subjects 2008 Controlled clinical trial n = 15

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