Ridgeway Jennifer L, Sundt Wendy J S, Krpata Tami S, Glasgow Amy, Smith Olivia A, Lampman Michelle A, Smith-Stellflug Jamie L, Menser Terri L, Juntunen Michael B, Liedl Chad P, Hentz Joseph G, McCoy Jessica J, McCoy Rozalina G
Division of Health Care Delivery Research; Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN, USA.
Research Services - Clinical Trials Office, Mayo Clinic, Rochester, MN, USA.
J Clin Transl Sci. 2024 Oct 17;8(1):e199. doi: 10.1017/cts.2024.646. eCollection 2024.
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.
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.
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.
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.
实用性试验旨在通过将研究程序融入常规护理环境来加速向实践的转化。本研究评估了与临床医生和患者招募以及参与社区护理(CP)试验相关的实施结果,并呈现了维持实用性研究特征的成功经验和挑战。
将处于院前环境、急诊科(ED)或因考虑转诊至ED/医院或继续住院接受中级护理的医院中的成年人按1:1随机分配至CP护理组或常规护理组。通过行政手段跟踪转诊和入组数据,并从电子健康记录(EHR)中提取患者特征。入组患者完成基线调查,对一部分干预组患者进行了访谈。邀请所有CP以及一部分临床医生和管理人员完成一项调查和访谈。
在2022年1月至2023年2月期间,240名入组患者(42%为农村患者)完成了调查,22名完成了访谈;63名工作人员完成了调查,20名完成了访谈。27个科室的93名临床医生至少进行了一次转诊。与转诊相关的因素包括项目认知度和对CP实践范围的理解。大多数患者在医院入组,但特征与初级护理人群相似,包括老年患者和病情复杂的患者。实现代表性面临的挑战包括有限的EHR基础设施、与患者同意相关的限制以及临床医生对患者随机分组打乱首选护理的担忧。
未来在繁忙临床环境中进行的实用性试验可能会受益于允许进行真实世界研究和代表性参与的监管政策和EHR功能。试验注册号:NCT05232799。