The acute effects of 3,4-methylenedioxymethamphetamine and d-methamphetamine on human cognitive functioning.
Con Stough, Rebecca King, Katherine Papafotiou, Phillip Swann, Edward Ogden, Keith Wesnes, Luke A. Downey
Psychopharmacology April 2012 DOI: 10.1007/s00213-011-2532-9 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Double-blind, placebo-controlled, within-subject laboratory study Peer reviewed |
|---|---|
| Sample size | 61 |
| Population | Abstinent recreational users of illicit drugs (33 females, 28 males; mean age 25.45 years) |
| Interventions | MDMA d-methamphetamine placebo |
| Dose | 100 mg MDMA; 0.42 mg/kg d-methamphetamine |
| Duration | Acute testing at 3 h (drug peak) and 24 h post-dose |
| Measures | trail-making measures, working memory index, choice reaction task |
| Topics | MDMA |
| Key points | At peak drug concentrations, MDMA was associated with poorer performance on trail-making measures and a trend-level working-memory index, while d-methamphetamine was associated with more accurate choice reaction task performance. Most performance differences between MDMA, methamphetamine, and placebo diminished by 24 hours, although some choice reaction time improvements persisted for methamphetamine. |
Abstract
This study investigated the acute (3-h) and 24-h post-dose cognitive effects of oral 3,4-methylenedioxymethamphetamine (MDMA), d-methamphetamine, and placebo in a within-subject double-blind laboratory-based study in order to compare the effect of these two commonly used illicit drugs on a large number of recreational drug users. Sixty-one abstinent recreational users of illicit drugs comprised the participant sample, with 33 females and 28 males, mean age 25.45 years. The three testing sessions involved oral consumption of 100 mg MDMA, 0.42 mg/kg d-methamphetamine, or a matching placebo. The drug administration was counter-balanced, double-blind, and medically supervised. Cognitive performance was assessed during drug peak (3 h) and at 24 h post-dosing time-points. Blood samples were also taken to quantify the levels of drug present at the cognitive testing time-points. Blood concentrations of both methamphetamine and MDMA at drug peak samples were consistent with levels observed in previous studies. The major findings concern poorer performance in the MDMA condition at peak concentration for the trail-making measures and an index of working memory (trend level), and more accurate performance on a choice reaction task within the methamphetamine condition. Most of the differences in performance between the MDMA, methamphetamine, and placebo treatments diminished by the 24-h testing time-point, although some performance improvements subsisted for choice reaction time for the methamphetamine condition. Further research into the acute effects of amphetamine preparations is necessary to further quantify the acute disruption of aspects of human functioning crucial to complex activities such as attention, selective memory, and psychomotor performance.
Comparable studies
Other randomized controlled trials on MDMA, most cited first.
Citations in the library
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- Cognitive functioning associated with acute and subacute effects of classic psychedelics and MDMA - a systematic review and meta-analysis. Scientific Reports June 26, 2024
- Subjective and neurocognitive profiling of clinical doses of 3,4-methylenedioxymethamphetamine (MDMA) in healthy volunteers: implications for therapeutic use Molecular Psychiatry April 8, 2026
- Strategic control, consolidation and poly-drug use; the relative contributions to verbal memory impairment in recreational ecstasy users UTAS Research Repository August 1, 2014
- Subacute and long-term changes in cognitive functioning after administration of classic psychedelics, MDMA and ketamine: A systematic review of clinical and preclinical evidence. Neuroscience & Biobehavioral Reviews August 14, 2026
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Cites 14
- Mood, cognition and serotonin transporter availability in current and former ecstasy (MDMA) users: the longitudinal perspective Journal of Psychopharmacology March 1, 2006
- Human Research on MDMA (3,4-Methylene- dioxymethamphetamine) Neurotoxicity: Cognitive and Behavioural Indices of Change Neuropsychobiology 2000
- The serotonin uptake inhibitor citalopram reduces acute cardiovascular and vegetative effects of 3, 4-methylenedioxymethamphetamine (‘Ecstasy’) in healthy volunteers Journal of Psychopharmacology May 1, 2000
- Dissociable Effects of a Single Dose of Ecstasy (MDMA) on Psychomotor Skills and Attentional Performance Journal of Psychopharmacology December 1, 2003
- Transient memory impairment after acute dose of 75mg 3.4-Methylene-dioxymethamphetamine Journal of Psychopharmacology November 1, 2005
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