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临床试验/NCT06138184
NCT06138184尚未招募不适用

Patient Education for Anticoagulants Using Learning Theories - a Pilot Study

University of Utah0 个研究点目标入组 68 人开始时间: 2026年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
68
主要终点
Feasibility of implementing a randomized control trial

研究概览

简要总结

The goal of this study is to test the feasibility of a randomized control trial evaluating the educational tool for anticoagulated patients.

Participants will be randomized to use new educational materials or current existing educational materials and answer survey questions.

详细描述

Eligible patients will be randomized using stratified block randomization to control for the type of anticoagulant (warfarin vs. DOAC) and status (naïve vs. experienced) to either the education intervention from Aim 2 or standard of care Data will be collected via online surveys before the intervention, immediately after, and then 3 months after the intervention.

Patients at the University of Utah Thrombosis Clinic will be recruited.

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

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

入选标准

  • initiating (naïve) or currently taking (experienced) oral anticoagulants with an anticipated treatment duration of at least three months
  • Experienced patients will be eligible if they score less than 75% on the Anticoagulation Knowledge Test

排除标准

  • Deficits in cognitive abilities, sensory input, or language significant enough to impede their use of the education tool and/or provision of written informed consent

结局指标

主要结局

Feasibility of implementing a randomized control trial

时间窗: 18 months

The study will be feasible if 1) the consent rate if 5 patients per month, 2) Proportion of patients completing the educational tool is 90%; 3) Loss to follow-up at three months is 20% or less

次要结局

  • Acceptability(3 months)
  • Acceptability - Educational Tool(At time of intervention)
  • Acceptability - Workflow Disruption(18 months)
  • Acceptability - Satisfaction(3 months)
  • Acceptability - Intervention/Survey Fatigue(3 months)

研究者

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

Aubrey E. Jones

Assistant Research Professor

University of Utah

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