Evidence map›Paper›PMID 42234418›Full record

SynthesisJAMA psychiatry2026

Evaluating Reduced Use and Abstinence as Outcomes in Pharmacotherapy Trials for Stimulant Use Disorder: A Meta-Analysis of 12 Randomized Controlled Trials.

Masoumeh Amin-Esmaeili, Mehdi Farokhnia, Ramin Mojtabai, Lorenzo Leggio, Renee M Johnson, Ryoko Susukida

Abstract readMeta-Analysis
In one paragraph

Synthesis in JAMA psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Masoumeh Amin-EsmaeiliDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Mehdi FarokhniaClinical Psychoneuroendocrinology and Neuropsychopharmacology Section, Translational Addiction Medicine Branch, National Institute on Drug Abuse Intramural Research Program and National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research, National Institutes of Health, Baltimore, Maryland.
Ramin MojtabaiDepartment of Psychiatry and Behavioral Sciences, Tulane Medical School, New Orleans, Louisiana.
Lorenzo LeggioClinical Psychoneuroendocrinology and Neuropsychopharmacology Section, Translational Addiction Medicine Branch, National Institute on Drug Abuse Intramural Research Program and National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research, National Institutes of Health, Baltimore, Maryland.
Renee M JohnsonDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Ryoko SusukidaDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Funding

Clinical Psychoneuroendocrinology and Neuropsychopharmacology (CPN)ZIADA000635 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI LEGGIO, LORENZO · 2020 to 2025
$15.2M
Intramural NIH HHS Z99 DA999999Intramural NIH HHS ZIA DA000635NIDA NIH HHS 75N95024P00505
6 · The paper itself

Abstract

Importance: Cocaine and methamphetamine use disorders are major public health challenges with no approved pharmacological treatments. Reliance on complete abstinence as the sole end point in randomized controlled trials (RCTs) may hinder identification of effective therapies, as it is often overly stringent, whereas reduced stimulant use is a promising alternative given its association with improved health outcomes. Objectives: To evaluate the treatment effect of pharmacological interventions tested in RCTs for stimulant use disorder, comparing reduced use to total abstinence. Design, Setting, and Participants: A meta-analysis was conducted of 12 US National Institute on Drug Abuse-sponsored multisite RCTs conducted between 2001 and 2011 evaluating pharmacological interventions among people seeking treatment for cocaine or methamphetamine dependence. One-stage individual participant meta-analysis was used, and analyses were performed between August 2024 and November 2025. Exposure: Tested pharmacotherapies included topiramate, bupropion, modafinil, ondansetron, tiagabine, cabergoline, reserpine, selegiline, and baclofen, each compared to placebo in double-blind trials. All participants received cognitive behavioral therapy regardless of treatment assignment. Main Outcomes and Measures: The primary outcome was reduced drug use based on self-report, defined as a transition from high frequency (≥5 days/month) to low frequency (1-4 days/month) of stimulant use or transition to abstinence. Abstinence, verified by urine toxicology, served as the secondary outcome. Mixed-effects logistic regression models with random study effects and inverse probability weighting were used to estimate pooled treatment effects. Results: A total of 2000 participants were included (1134 in cocaine RCTs and 866 in methamphetamine RCTs), of whom 587 (29.4%) were women, with a mean (SD) age of 39.7 (8.6) years. Overall, 446 participants (31.2%, weighted) achieved reduced use, whereas 184 (13.3%, weighted) achieved abstinence at the trial end point. No significant differences were observed between the pooled active treatment and placebo groups for either outcome, overall or when stratified by stimulant type. In analyses of individual medications, cabergoline showed positive effect sizes (Cohen h, 0.352; 95% CI, 0.115-0.590), indicating significantly higher rates of reduced cocaine use with cabergoline than pooled placebo. Conclusions and Relevance: The present findings of this meta-analysis underscore the importance of evaluating a continuum of outcomes rather than focusing solely on abstinence in RCTs. The results suggest that reductions in stimulant use may serve as meaningful efficacy signals that could be underestimated when relying solely on stringent outcomes, such as abstinence.

Indexed as

Amphetamine-Related DisordersCentral Nervous System StimulantsCocaine-Related DisordersRandomized Controlled Trials as TopicHumansMethamphetamineTreatment OutcomeCentral Nervous System StimulantsMethamphetamine

Identifiers

PMID42234418
PMCPMC13234748

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.