临床试验/NCT03840018

NCT03840018已完成不适用

Randomized Trial to Assess the Effectiveness of a Postal Intervention for Reducing the Chronic Use of Highe Doses of Proton Pump Inhibitors

Osakidetza2 个研究点分布在 1 个国家目标入组 401 人开始时间: 2017年5月10日最近更新: 2019年2月15日

适应症

干预措施

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 401
试验地点: 2
主要终点: Active prescriptions of each proton pump inhibitors dose after the intervention

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

It was a randomised intervention study, with before-and-after outcome measures and a control group, in patients who had an active long-term prescription for PPIs at high doses for at least 6 months.

详细描述

The intervention consisted of sending patients an informative letter by post, in which their doctor invited them to seek an appointment for a medication review. Control group patients did not receive such a letter, and they were treated as usual (their doctors received a list of identifiers of patients on high doses).

The main outcome variable was the number of active prescriptions of each PPI dose (high dose/standard dose/treatment cessation) at 6 months after the intervention.

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: Single (Care Provider)

入排标准

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

入选标准

•Patients under the care of our organisation who in May 2017 had an active long-term prescription for PPIs at high doses for at least 6 months.

排除标准

•Patients whose GPs declined to participate

研究组 & 干预措施

Control

No Intervention

Sending doctors the lists of patients that meet the inclusion criteria to have their treatment reviewed

Letter by post to patients

Other

Patients were sent a letter explaining the risks of using PPIs at long-term high doses and encouraging them to visit their doctor

干预措施: Letter by post to patients (Other)

结局指标

主要结局

Active prescriptions of each proton pump inhibitors dose after the intervention

时间窗: 6 months

Number of active prescriptions of each proton pump inhibitors dose (high dose/standard dose/treatment cessation) at 6 months after the intervention

次要结局

未报告次要终点

研究者

发起方

Osakidetza

申办方类型

Other

责任方

Principal Investigator

主要研究者

Elena Valverde

Primary care pharmacist

Osakidetza

研究点 (2)

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