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临床试验/NCT07098143
NCT07098143尚未招募不适用

Individualized Risk Factor Management Application for Reducing the Recurrence Risk of Stroke: A Multicenter, Randomized Controlled Trial Study

Xuanwu Hospital, Beijing0 个研究点目标入组 5,092 人开始时间: 2025年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
5,092
主要终点
1-year recurrence rate of stroke

研究概览

简要总结

This study applied an application that provides personalized suggestions and explore the effect of this actual intervention on reducing the risk of stroke recurrence

详细描述

This study applied an application that provides personalized suggestions based on participant's own secondary prevention risk factors status to stroke patients, enabling them to promptly take protective measures. And explore the effect of this actual intervention on reducing the risk of stroke recurrence after one year, as well as changes in other health-related indicators.

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
None

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged 40 to 80, with no gender restrictions;
  • •Acute ischemic stroke inpatients within 2 weeks of onset, where the onset time is the time when stroke symptoms appear or the last known normal time of the patient (when it is an onset during sleep or the symptom onset time cannot be accurately obtained due to aphasia, impaired consciousness, etc.);
  • •Confirmed diagnosis of ischemic stroke by CT or MRI of the brain within 2 weeks after symptom onset; ④ Local residents (residing for ≥6 months); ⑤ Patients who voluntarily participate in the study, have high compliance, and can sign the informed consent form;
  • •Patients who own a smartphone or other smart devices.

排除标准

  • •Patients diagnosed with other cerebrovascular diseases (hemorrhagic stroke, transient ischemic attack, cerebral venous sinus thrombosis, etc.) or non-cerebrovascular diseases;
  • •Known pregnant or lactating women, or those who tested positive on a pregnancy test before cluster randomization;
  • •Patients with other conditions that may affect participation in the trial (e.g., refractory hypertension, severe aphasia, etc.);
  • •Patients undergoing psychiatric/psychological treatment that may contaminate the results; ⑤ Patients with a life expectancy of less than one year (e.g., coexisting malignant tumors, severe cardiopulmonary diseases, etc.);
  • •Patients already participating in other interventional clinical studies that may influence the outcome assessment; ⑦ Patients for whom the investigator deems unsuitable for participation in this study or who may pose significant risks to the patients (e.g., cognitive impairment preventing understanding and/or compliance with the study procedures and/or follow-up).

研究组 & 干预措施

Risk factor management group

Experimental

干预措施: Risk factor management (Other)

Routine education

No Intervention

结局指标

主要结局

1-year recurrence rate of stroke

时间窗: Intervention at the 1-year

次要结局

  • System usability scale score(Intervention at 3-month, 6-month, 9-month and 1-year)
  • NIH stroke scale score(Baseline)
  • 3-month, 6-month, 9-month recurrence rate of stroke(Intervention at 3-month, 6-month, 9-month)
  • Blood pressure(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • C-reactive protein(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Modified rankin scale score(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Health literacy scale score(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Prothrombin time(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Minimum mental state examination(Baseline; Intervention at 6-month and 1-year)
  • Social support rate scale score(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Electrocardiogram (ECG) parameters(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Fasting blood glucose(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • International normalized ratio(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Platelet count(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • D-dimer(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • European five-dimensional five-level health scale score(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Depression anxiety stress scales - 21 score(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)
  • Activated partial thromboplastin time(Baseline; Intervention at 3-month, 6-month, 9-month and 1-year)

研究者

申办方类型
Other
责任方
Sponsor

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