跳至主要内容
临床试验/NCT03738826
NCT03738826已完成不适用

Reducing Disparities in Medication Adherence of Patients With Systemic Lupus Erythematosus (SLE)

Duke University2 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2019年10月2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
135
试验地点
2
主要终点
Acceptability as Measured by Provider Survey

研究概览

简要总结

This is a pilot study to assess the feasibility of using Surescripts refill data during the clinical encounter to improve medication adherence in patients with systemic lupus erythematosus

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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

  • - All followup patients seen at the Duke Lupus clinic

排除标准

  • Patients not seen at the Duke Lupus Clinic
  • New patients seen for the first time at the Duke Lupus Clinic
  • Patients who are not prescribed any lupus medications

研究组 & 干预措施

Intervention arm

Experimental

Lupus clinic providers will use Surescripts refill information to assess adherence level and address adherence barriers. We will assess the feasibility and acceptability of the intervention.

干预措施: Behavioral Intervention (Behavioral)

结局指标

主要结局

Acceptability as Measured by Provider Survey

时间窗: 12 weeks

Acceptability as measured by provider survey, score range 1-5, with a higher score indicating that the intervention was more acceptable.

Feasibility as Measured by Number of Participants With EMR (Electronic Medical Record) Documentation of Adherence

时间窗: 12 weeks

Feasibility as measured by documentation of adherence assessment made by provider.

次要结局

  • Percentage of Adherent Participants as Determined by Medication Possession Ratio (MPR)(Baseline, 12 weeks)
  • Medication Adherence as Determined by Self Report(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验