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临床试验/NCT02511093
NCT02511093Unknown不适用

A Team-Based Care for Hypertension Management (TBC-HTA): A Randomized Controlled Study

Centre Hospitalier Universitaire Vaudois2 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
110
试验地点
2
主要终点
Difference in the proportion of patients with controlled blood pressure (daytime ABPM <135/85 mmHg) at 6-month between TBC and usual care patients

研究概览

简要总结

The purpose of this study is to determine whether a team-based care (TBC) intervention, combining physician, nurse and pharmacist care improves BP control compared to usual care at 6 months among outpatients with uncontrolled hypertension.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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

  • treated patients with uncontrolled hypertension (defined as daytime systolic/diastolic ambulatory blood pressure monitoring (ABPM) ≥135/85mmHg) taking one or two antihypertensive medications;
  • speak and understand French;
  • agree to use the same pharmacy's services for the whole duration of the study.

排除标准

  • unable to understand the study aim;
  • pregnancy and lactating;
  • livimg in a nursing home;
  • hospitalization during the recruitment period;
  • participation in another study;
  • daytime ABPM>180/110 mmHg.

结局指标

主要结局

Difference in the proportion of patients with controlled blood pressure (daytime ABPM <135/85 mmHg) at 6-month between TBC and usual care patients

时间窗: 6-month

Difference in the proportion of patients with controlled blood pressure (daytime ABPM \<135/85 mmHg) at 6-month between TBC and usual care patients

Difference in daytime ABPM at 6-month between TBC and usual care patients

时间窗: 6-month

Difference in daytime ABPM at 6-month between TBC and usual care patients

次要结局

  • Patients and healthcare professionals' acceptance and satisfaction with the TBC-intervention(6-month)
  • Difference in the proportion of TBC and usual care patients with controlled blood pressure (daytime ABPM <135/85 mmHg) at 12-month (6 months after intervention stopped)(12-month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Valérie Santschi

Dr. Valérie Santschi, PharmDipl, PhD

Centre Hospitalier Universitaire Vaudois

研究点 (2)

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