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临床试验/NCT05218343
NCT05218343已完成不适用

Modifying Default Dosing During Electronic Prescribing to Impact Prescribing of High-risk Drugs in Hospitalized Elderly Patients: A Cluster Randomized Controlled Trial With Crossover

Icahn School of Medicine at Mount Sinai2 个研究点 分布在 1 个国家目标入组 8,640 人开始时间: 2022年2月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
8,640
试验地点
2
主要终点
Prescription rate of modified default dose for eight high-risk drugs

研究概览

简要总结

This study will assess whether a modification in the default dose and frequency (the first option a provider sees) during electronic prescribing of a high-risk drug can impact prescribing behavior and subsequent changes in average dose for the targeted high-risk drug, when prescribed to a hospitalized patient aged ≥65 years. In this cluster randomized crossover (CRXO) trial we will randomize a non-intrusive "nudge" intervention, which involves modifying the default dose for high-risk drugs when prescribed electronically to hospitalized patients aged ≥65 years. The CRXO trial involves 10 sites in an urban health system: five sites will start the trial under the intervention/control during a first time period (T1) after which they switch intervention/control status (T2). The primary outcome is prescription rate of a lower default dose (i.e. the geriatric standard) for 8 high-risk drugs. This study will inform the effectiveness of EHR-based "nudge" interventions to reduce inappropriate prescribing of high-risk drugs for elderly patients.

Analyses ongoing, expected to finalize spring 2023

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
Double (Participant, Care Provider)

盲法说明

Participants and care providers will be unaware of the intervention. However, prescribers will be able to prescribe all available doses, without any restrictions

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • a patient must be hospitalized
  • 65-years old or older
  • receive one of the targeted medications

排除标准

  • 未提供

研究组 & 干预措施

Control

No Intervention

No change in default dose or frequency selected for the eight targeted drugs

Intervention

Experimental

The first option a prescriber sees when prescribing any of eight high-risk drugs for elderly hospitalized patients will be modified; the first frequency option a prescriber sees will be modified as well. Providers retain the ability to prescribe any dose or frequency.

干预措施: EHR-based "nudge" interventions (Behavioral)

结局指标

主要结局

Prescription rate of modified default dose for eight high-risk drugs

时间窗: 24 weeks

Rate at which the modified default dose (geriatric standard) and frequency for eight high-risk drugs are prescribed.

次要结局

  • Mean per-patient dose(24 weeks)
  • Rate of 30-day readmissions(30 days post-discharge regarding hospitalization during which a high-risk drug was prescribed)
  • Length of hospital stay(24 weeks)
  • Cost of hospital stay(24 weeks)
  • Spillover effects to patients aged <65(24 weeks)
  • Drug-specific prescription rate(24 weeks)
  • Rate of inpatient falls(24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jashvant Poeran

Associate Professor Depts. of Population Health Science & Policy / Orthopedics / Medicine Director, Center for Clinical and Outcomes Research

Icahn School of Medicine at Mount Sinai

研究点 (2)

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