Back to Search Start Over

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

Authors :
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
Source :
Journal of Clinical and Translational Science, Vol 8 (2024)
Publication Year :
2024
Publisher :
Cambridge University Press, 2024.

Abstract

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.

Details

Language :
English
ISSN :
20598661
Volume :
8
Database :
Directory of Open Access Journals
Journal :
Journal of Clinical and Translational Science
Publication Type :
Academic Journal
Accession number :
edsdoj.73e241476b9f4c58866f751120116574
Document Type :
article
Full Text :
https://doi.org/10.1017/cts.2024.646