Feasibility of Implementing a Pharmacist-Integrated Collaborative Model for Opioid Use Disorder: A Nonrandomized Clinical Trial - Summary - MDSpire
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Assessing the Feasibility of a Pharmacist-Integrated Collaborative Care Model for Opioid Use Disorder: A Nonrandomized Clinical Trial

  • By

  • Felicity Homsted

  • David A. Fiellin

  • Udi E. Ghitza

  • Vernon T. Gardner

  • Bethany McLeman

  • Paul J. Joudrey

  • Gerald Cochran

  • Sarah K. Moore

  • Lisa Saldana

  • Edward Chongsi

  • Kimberly Kramer

  • Ashley Vena

  • Rebecca A. Ottesen

  • Jacklyn Harris

  • Jesse S. Boggis

  • Deepika Rao

  • Owen Murray

  • Scott Gerlach

  • Phoebe Gauthier

  • Katie P. Osterhage

  • Laura-Mae Baldwin

  • Lisa A. Marsch

  • October 14, 2026

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Objective:

To assess the feasibility and acceptability of implementing pharmacist-integrated medication treatment for opioid use disorder (PrIMO) in varied primary care settings, and to examine preliminary implementation outcomes.

Approach:
  • Design and setting: A nonrandomized, unassigned, unblinded mixed-methods longitudinal feasibility and implementation trial conducted at four primary care sites in the Northeast, Midwest, Northwest, and Southwest US from August 2022 to July 2024.
  • Intervention: PrIMO integrated pharmacists into interdisciplinary OUD care teams. Its six core components were collaborative communication, weekly clinical huddles, provider and patient education, comorbidity screening, and education for local partners.
  • Assessment: The primary feasibility measure was the Stages of Implementation Completion instrument, tailored to 61 milestones. Launch of services was the binary feasibility indicator. Staff and patient surveys assessed acceptability and other implementation outcomes.
Key Findings:
  • The supplied article context describes the study design, intervention, and planned outcome measures but does not report trial results.
Interpretation:

The study was designed to evaluate whether PrIMO could be implemented across diverse primary care settings; the provided context does not establish its results.

Limitations:
  • The study was nonrandomized, unassigned, and unblinded.
  • The project duration was insufficient for a true assessment of sustainability.
Sources:

Original Source(s)

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