NCT06290440尚未招募不适用
Development of Medication Counselling Models for Outpatient Oral Anticoagulant-taking Patients
Gia Dinh People Hospital0 个研究点目标入组 360 人开始时间: 2024年6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
- 发起方
- 入组人数
- 360
- 主要终点
- Medication adherence
研究概览
简要总结
The goal of this clinical trial is to investigate whether telepharmacy-led counselling can improve medication adherence, knowledge, and hospitalisation/mortality compared with pharmacist-led counselling in adult outpatients taking oral anticoagulants.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 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
- 是
入选标准
- •≥18 years old
- •taking oral anticoagulants
- •using smartphones that can access the telepharmacy application
- •agreeing to participate
排除标准
- •pregnancy or lactation
- •having cancer
- •having immunodeficiency disorders or using immunosuppressants
- •renal impairment (creatinine clearance <30 mL/min)
- •hepatic impairment (Child-Pugh B or C cirrhosis)
- •heart failure (class IV, New York Heart Association)
- •history of myocardial infarction or stroke within the latest 2 months
结局指标
主要结局
Medication adherence
时间窗: Measured at month 1, 6, and 12 after randomisation
Measured using Morisky-Green-Levine scale. The levels of adherence are: (1) high (0 point); (2) medium (1-2 points); and (3) low (3-4 points).
次要结局
- Knowledge of oral anticoagulants(Measured at month 1, 6, and 12 after randomisation)
- All-cause hospitalisation(24 months after randomisation)
- All-cause mortality(24 months after randomisation)
- VTE-related mortality(24 months after randomisation)
- Bleeding-related mortality(24 months after randomisation)
- VTE-related hospitalisation(24 months after randomisation)
- Bleeding-related hospitalisation(24 months after randomisation)
研究者
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