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临床试验/NCT01115660
NCT01115660已完成不适用

AVAIL interVention Trial (Adherence Evaluation After Ischemic Stroke - Longitudinal): Pilot Protocol

Duke University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2010年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
Feasibility of Intervention (Ability to Reach Patients at 3 Months)

研究概览

简要总结

The objectives of the trial of a medication-coach program for patients with stroke or transient ischemic attack are to pilot test the study design, the intervention components and the data collection forms and refine them for a larger trial whose goal will be to improve long-term adherence to stroke prevention medications.

研究设计

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

入排标准

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

入选标准

  • Patients at Wake Forest University Baptist Medical Center (WFUBMC) over age 18
  • Diagnosed with acute ischemic stroke, transient ischemic attack or intracranial hemorrhage
  • provide consent to participate

排除标准

  • discharged to nursing home, acute rehabilitation center, inpatient hospice, or other acute hospital
  • non-English speakers
  • patient and proxy unable to participate in telephone conversation

结局指标

主要结局

Feasibility of Intervention (Ability to Reach Patients at 3 Months)

时间窗: 3 months

Number of patients contacted at 3 months

次要结局

  • Follow up Appointment With MD(3 months)

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (2)

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