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Addressing COVID-19 Barriers to Clinical Trial Enrollment and Implementation in the PHARM-DC Study
Abstract   Open access   Peer reviewed

Addressing COVID-19 Barriers to Clinical Trial Enrollment and Implementation in the PHARM-DC Study

Joshua Pevnick, Michelle Keller, Korey Kennelty, Michelle Ko, Logan Murry, An Nguyen, Andrew Henreid and Jeffrey Schnipper
Innovation in aging, Vol.5(Suppl. 1), p.103
01/01/2021
DOI: 10.1093/geroni/igab046.393
PMCID: PMC8680858
url
https://doi.org/10.1093/geroni/igab046.393View
Published (Version of record) Open Access

Abstract

Abstract 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.
Clinical sciences

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