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.
Citations in the library
Cited by 18
- Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review Journal of Psychopharmacology August 26, 2022
- Preliminary safety and effectiveness of psilocybin-assisted therapy in adults with fibromyalgia: an open-label pilot clinical trial Frontiers in Pain Research March 18, 2025
- Pharmacological and non-pharmacological predictors of the LSD experience in healthy participants. Translational Psychiatry September 4, 2024
- Therapeutic role of psilocybin and 3,4-methylenedioxymethamphetamine in trauma: A literature review World Journal of Psychiatry May 19, 2023
- Study protocol for “MDMA-assisted therapy as a treatment for major depressive disorder: A proof of principle study” Frontiers in Psychiatry October 26, 2022
and 13 more in the library
Cites 17
- MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study. Nature Medicine June 1, 2021
- 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. The Lancet Psychiatry May 1, 2018
- Hallucinogenic Amphetamine Selectively Destroys Brain Serotonin Nerve Terminals Science September 6, 1985
- 3,4-Methylenedioxymethamphetamine (MDMA) neurotoxicity in rats: a reappraisal of past and present findings Psychopharmacology March 15, 2006
- The Effects of Acutely Administered 3,4-Methylenedioxymethamphetamine on Spontaneous Brain Function in Healthy Volunteers Measured with Arterial Spin Labeling and Blood Oxygen Level–Dependent Resting State Functional Connectivity Biological Psychiatry January 10, 2014
and 12 more in the library