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Efficacy of a brief multifactorial adherence-based intervention on reducing the blood pressure of patients with poor adherence: protocol for a randomized clinical trial

机译:简短的基于多因素依从性干预对降低依从性差患者血压的功效:一项随机临床试验方案

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Background Lowering of blood pressure by antihypertensive drugs reduces the risks of cardiovascular events, stroke, and total mortality. However, poor adherence to antihypertensive medications reduces their effectiveness and increases the risk of adverse events. In terms of relative risk reduction, an improvement in medication adherence could be as effective as the development of a new drug. Methods/Design The proposed randomized controlled trial will include patients with a low adherence to medication and uncontrolled blood pressure. The intervention group will receive a multifactorial intervention during the first, third, and ninth months, to improve adherence. This intervention will include motivational interviews, pill reminders, family support, blood pressure self-recording, and simplification of the dosing regimen. Measurement The primary outcome is systolic blood pressure. The secondary outcomes are diastolic blood pressure, proportion of patients with adequately controlled blood pressure, and total cost. Discussion The trial will evaluate the impact of a multifactorial adherence intervention in routine clinical practice. Ethical approval was given by the Ethical Committee on Human Research of Balearic islands, Spain (approval number IB 969/08 PI). Trial registration Current controlled trials ISRCTN21229328
机译:背景技术通过降压药物降低血压可降低心血管事件,中风和总死亡率的风险。但是,对降压药的依从性差会降低其有效性,并增加发生不良事件的风险。在降低相对风险方面,药物依从性的改善可能与新药的开发一样有效。方法/设计拟议的随机对照试验将包括对药物依从性低且血压不受控制的患者。干预组将在第一,第三和第九个月接受多因素干预,以提高依从性。这项干预措施将包括动机访谈,催眠药,家庭支持,血压自我记录以及简化用药方案。测量主要结果是收缩压。次要结果是舒张压,血压得到适当控制的患者比例以及总费用。讨论该试验将评估常规临床实践中多因素依从性干预的影响。西班牙巴利阿里群岛人类研究伦理委员会已批准了伦理(批准号IB 969/08 PI)。试用注册当前对照试验ISRCTN21229328

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