此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Smart Phone Application in the Secondary Clinical Prevention Management for Chinese Patients (SPASCPM)

Effects of a Smart Phone Application in the Secondary Clinical Prevention Management for Chinese Patients After Coronary Intervention Treatment: a Randomized Controlled Trial

The purpose of the study is to investigate the effects of smart phone app on the secondary prevention for patients with coronary heart disease post percutaneous coronary intervention.

研究概览

详细说明

The secondary prevention for patients with coronary heart disease post percutaneous coronary intervention (PCI) proved associated with a significant reduction in mortality rates and improvement in quality of life. For the limitation of socio-economic conditions, not all patients post PCI are in a position to receive continuous standardized secondary prevention management. Therefore a smart phone app for secondary prevention management post PCI will be installed on patients' smart phones in order to investigate its effects on risk factors control, medication compliance, as well as quality of life and adverse cardiac events in the next six months post discharge. Participants allocated to the control group will receive a booklet with general advice on secondary prevention of coronary heart disease. Patients in app group and control group will be interviewed by telephone at the 2nd week and the 3rd month, and at the 1st month and 6th month they will return our hospital for face to face follow-up and to compliance and medication adjustment, assessment of life quality, risk factors control and medication adherence.

研究类型

介入性

注册 (实际的)

86

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • First diagnosis of coronary heart disease and received a PCI treatment.
  • Age 18-65 years.
  • Able and willing to provide written informed consent.

Exclusion Criteria:

  • Speech communication barriers.
  • Patients with a clear history of allergies to anti-platelet drugs.
  • Patients with a clear history of allergies to anti-platelet ᵦ-blockers.
  • Patients with a clear history of allergies to statin drugs.
  • Patients with a clear history of allergies to antihypertensive drugs.
  • Patients with a clear history of allergies to antidiabetic drugs.
  • Patients with serious heart failure(better than NYHA class II).
  • Patients with cerebral infarction or cerebral hemorrhage.
  • Patients with liver dysfunction (AST and ALT> 2 times that of the reference value).
  • Patients with kidney dysfunction (creatinine clearance rate< 60ml/min).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Smart phone app
The app contains education materials for secondary prevention of coronary artery disease. So patients can access them very easily. The app pushes heath management recommendation information on the timeline after percutaneous coronary intervention, and also provides health care lecture to help patients to improve their secondary prevention. And online or telephone consultation ways are integrated into the App to provide convenience for patients to communicate with health care professionals.
App for this study is provided with real time updating educational materials, reminder, and consultation for improving secondary prevention, and the related information is pushed to a patient in chronological order after his or her PCI operation.
其他:Control group
Participants allocated to the control group will receive a booklet with general advice on secondary prevention of coronary artery disease.
A guideline booklet with general advice on secondary prevention of coronary artery disease.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in quality of life
大体时间:Baseline and 1 and 6 months
Seatt1e Angina Questionnaire
Baseline and 1 and 6 months

次要结果测量

结果测量
措施说明
大体时间
Change in medication compliance
大体时间:Baseline and 1 and 6 months
Percent of prescribed antiplatelet drug,ᵦ-blocker,angiotensin converting enzyme inhibitor,angiotensin II receptor blocker and statins taken during the past 1 and 6 monthers
Baseline and 1 and 6 months
Change in systolic blood
大体时间:Baseline and 1 and 6 months
systolic blood pressure is measured via pressuremercury sphygmomanometer and recored in the unit of mmHg.
Baseline and 1 and 6 months
Change in diastolic blood pressure
大体时间:Baseline and 1 and 6 months
Diastolic blood pressure is measured via pressuremercury sphygmomanometer and recored in the unit of mmHg.
Baseline and 1 and 6 months
Changes in serum total cholesterol
大体时间:Baseline and 1 and 6 months
Serum total cholesterol is measured by automatic biochemistry analyzer and recorded in the unit of mmol/L.
Baseline and 1 and 6 months
Changes in serum triglyceride
大体时间:Baseline and 1 and 6 months
Serum triglyceride is measured by automatic biochemistry analyzer and recorded in the unit of mmol/L.
Baseline and 1 and 6 months
Changes in serum high-density lipoproteincholesterol
大体时间:Baseline and 1 and 6 months
Serum high-density lipoproteincholesterol is measured by automatic biochemistry analyzer and recorded in the unit of mmol/L.
Baseline and 1 and 6 months
Changes in serum low-density lipoproteincholesterol
大体时间:Baseline and 1 and 6 months
Serum low-density lipoproteincholesterol is measured by automatic biochemistry analyzer and recorded in the unit of mmol/L.
Baseline and 1 and 6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Jingwen Hu, Master、First Affiliated Hospital Xi'an Jiaotong University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2016年9月20日

初级完成 (实际的)

2017年4月1日

研究完成 (实际的)

2017年5月1日

研究注册日期

首次提交

2016年7月13日

首先提交符合 QC 标准的

2016年7月27日

首次发布 (估计)

2016年7月28日

研究记录更新

最后更新发布 (实际的)

2022年5月25日

上次提交的符合 QC 标准的更新

2022年5月19日

最后验证

2016年4月1日

更多信息

与本研究相关的术语

其他研究编号

  • XAJTUFH2016
  • 2016JM8116 (其他赠款/资助编号:Science and Technology Department of Shaanxi Province, China)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅