
Addressing COVID-19 Barriers to Clinical Trial Enrollment and Implementation in the PHARM-DC Study
Author(s) -
Joshua M. Pevnick,
Michelle S. Keller,
Korey A. Kennelty,
Michelle Ko,
Logan T. Murry,
An Nguyen,
Andrew J. Henreid,
Jeffrey L. Schnipper
Publication year - 2021
Publication title -
innovation in aging
Language(s) - English
Resource type - Journals
ISSN - 2399-5300
DOI - 10.1093/geroni/igab046.393
Subject(s) - medicine , pharmacist , pharmacy , pandemic , medication reconciliation , randomized controlled trial , psychological intervention , covid-19 , clinical trial , clinical pharmacy , family medicine , adverse effect , intervention (counseling) , medical emergency , nursing , pharmacology , disease , infectious disease (medical specialty)
Recent hospitalization puts older adults at higher risk of experiencing adverse drug events (ADEs) that are a common cause of hospital readmission. Yet, most ADEs are preventable. The PHARMacist Discharge Care (PHARM-DC) study is a multi-site randomized controlled trial that seeks to evaluate the effect of pharmacist-led peri- and post-discharge interventions on 30-day hospital readmissions among older adults taking ≥10 medications or ≥3 high-risk medications. The PHARM-DC intervention includes pharmacist-led patient counseling, medication reconciliation at discharge, and a follow-up phone call post-discharge. We will highlight study protocol adaptations undertaken during the COVID-19 pandemic to address challenges to enrollment and to minimize risk of COVID-19 exposure for study participants and research personnel. Additionally, we will share insights from focus groups and semi-structured interviews with pharmacist interventionists and pharmacy leaders on barriers and facilitators to implementation due to the pandemic and strategies for future clinical trials to overcome barriers.
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