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临床试验/NCT04333238
NCT04333238已完成不适用

Notation Optimization Through Template Engineering

Johns Hopkins University2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2017年1月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
2
主要终点
Note evaluation by authors using a likert scale

研究概览

简要总结

This is a randomized non-blinded controlled trial of a standard note template versus a redesigned note template using a simulated patient encounter and the electronic medical record.

详细描述

Residents documented the simulated patient encounter using one of two templates. The standard template was based on the usual outpatient progress note. The new template placed the assessment and plan section in the beginning, grouped subjective data into the assessment section, and deemphasized elements not related to the current presentation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Residents who had open visit slots during their outpatient clinic time

排除标准

  • 未提供

结局指标

主要结局

Note evaluation by authors using a likert scale

时间窗: Immediately after note entry, up to 1 hour

Likert-scale survey instrument evaluating perceived organization, structure, and efficiency of note.

Note length

时间窗: Duration of note entry, up to 2 hours

Note length in line count.

Time to note completion

时间窗: Duration of note entry, up to 2 hours

Time to note completion in minutes.

Note evaluation by reviewers using the Physician Documentation Quality Instrument

时间窗: Within 1 year

Physician Documentation Quality Instrument (PDQI-9) - validated note quality scale composed of 9 metrics. 1 is not at all. 5 is extremely.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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