Journal of Clinical and Translational Science (Jan 2024)

Evaluating adoption and reach in a pragmatic randomized trial of community paramedicine for intermediate acuity patient care

  • Jennifer L. Ridgeway,
  • Wendy J. S. Sundt,
  • Tami S. Krpata,
  • Amy Glasgow,
  • Olivia A. Smith,
  • Michelle A. Lampman,
  • Jamie L. Smith-Stellflug,
  • Terri L. Menser,
  • Michael B. Juntunen,
  • Chad P. Liedl,
  • Joseph G. Hentz,
  • Jessica J. McCoy,
  • Rozalina G. McCoy

DOI
https://doi.org/10.1017/cts.2024.646
Journal volume & issue
Vol. 8

Abstract

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Abstract Introduction: Pragmatic trials aim to speed translation to practice by integrating study procedures in routine care settings. This study evaluated implementation outcomes related to clinician and patient recruitment and participation in a trial of community paramedicine (CP) and presents successes and challenges of maintaining pragmatic study features. Methods: Adults in the pre-hospital setting, emergency department (ED), or hospital being considered for referral to the ED/hospital or continued hospitalization for intermediate-level care were randomized 1:1 to CP care or usual care. Referral and enrollment data were tracked administratively, and patient characteristics were abstracted from the electronic health record (EHR). Enrolled patients completed baseline surveys, and a subset of intervention patients were interviewed. All CPs and a sample of clinicians and administrators were invited to complete a survey and interview. Results: Between January 2022 and February 2023, 240 enrolled patients (42% rural) completed surveys, and 22 completed an interview; 63 staff completed surveys and 20 completed an interview. Ninety-three clinicians in 27 departments made at least one referral. Factors related to referrals included program awareness and understanding the CP practice scope. Most patients were enrolled in the hospital, but characteristics were similar to the primary care population and included older and medically complex patients. Challenges to achieving representativeness included limited EHR infrastructure, constraints related to patient consenting, and clinician concerns about patient randomization disrupting preferred care. Conclusion: Future pragmatic trials in busy clinical settings may benefit from regulatory policies and EHR capabilities that allow for real-world study conduct and representative participation. Trial registration: NCT05232799.

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