Artificial Intelligence in Depression–Medication Enhancement (AID-ME): A Cluster Randomized Trial of a Deep-Learning-Enabled Clinical Decision Support System for Personalized Depression Treatment Selection and Management

  • David Benrimoh
  • , Kate Whitmore
  • , Maud Richard
  • , Grace Golden
  • , Kelly Perlman
  • , Sara Jalali
  • , Timothy Friesen
  • , Youcef Barkat
  • , Joseph Mehltretter
  • , Robert Fratila
  • , Caitrin Armstrong
  • , Sonia Israel
  • , Christina Popescu
  • , Jordan F. Karp
  • , Sagar V. Parikh
  • , Shirin Golchi
  • , Erica E.M. Moodie
  • , Junwei Shen
  • , Anthony J. Gifuni
  • , Manuela Ferrari
  • Mamta Sapra, Stefan Kloiber, Georges F. Pinard, Boadie W. Dunlop, Karl Looper, Mohini Ranganathan, Martin Enault, Serge Beaulieu, Soham Rej, Fanny Hersson-Edery, Warren Steiner, Alexandra Anacleto, Sabrina Qassim, Rebecca McGuire-Snieckus, Howard C. Margolese

Research output: Contribution to journalArticlepeer-review

Abstract

Background: There has been increasing interest in the use of artificial intelligence (AI)-enabled clinical decision support systems (CDSS) for the personalization of major depressive disorder (MDD) treatment selection and management, but clinical studies are lacking. We tested whether a CDSS that combines an AI which predicts remission probabilities for individual antidepressants and a clinical algorithm based on treatment can improve MDD outcomes. Methods: This was a multicenter, cluster randomized, patient-and-rater blinded and clinician-partially-blinded, active-controlled trial that recruited outpatient adults with moderate or greater severity MDD. All patients had access to a patient portal to complete questionnaires. Clinicians in the active group had access to the CDSS; clinicians in the active-control group received patient questionnaires; both groups received guideline training. Primary outcome was remission (<11 points on the Montgomery-Asberg Depression Rating Scale [MADRS]) at study exit. Results: Forty-seven clinicians were recruited at 9 sites. Of 74 eligible patients, 61 patients completed a postbaseline MADRS and were analyzed. There were no differences in baseline MADRS (P= .153). There were more remitters in the active (n = 12, 28.6%) than in the active-control (0%) group (P=.012, Fisher’s exact). Of 3 serious adverse events, none were caused by the CDSS. Speed of improvementwashigherintheactivethan the control group (1.26 vs 0.37, P=.03). Conclusions: While limited by sample size and the lack of primary care clinicians, these results demonstrate preliminary evidence that longitudinal use of an AI-CDSS can improve outcomes in moderate and greater severity MDD.

Original languageEnglish (US)
Article number24m15634
JournalJournal of Clinical Psychiatry
Volume86
Issue number3
DOIs
StatePublished - Sep 2025
Externally publishedYes

ASJC Scopus subject areas

  • Psychiatry and Mental health

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