Secondary Prevention of Ischemic Stroke and Transient Ischemic Attack With an Intelligent Management System
Recruiting now · Not applicable
Conditions studied: Ischemic Stroke, Transient Ischemic Attack (TIA)
In brief
The purpose of this study is to develop a digital health-based intelligent management system for the secondary prevention of ischemic stroke and to evaluate its effectiveness through a multicenter randomized controlled trial, assessing its health economic value. Participants will receive usual care after discharge (control group) or be managed with a WeChat-based intelligent management system after discharge (intervention group). At one year, all patients will undergo face-to-face follow-up to assess clinical events, medication adherence, and the achievement of target risk factor levels.
Key facts
- Study ID
- NCT06783049
- Run by
- Beijing Tiantan Hospital
- People needed
- 4490
- Starts
- 2025-03-03
- Expected to finish
- 2027-01-31
- Last updated by the study team
- 2026-01-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years.
- Patients diagnosed with acute ischemic stroke or transient ischemic attack.
- Time from onset to enrollment ≤ 14 days.
- Presence of at least one modifiable risk factor (hypertension, diabetes).
- Ability to independently use a smartphone to complete system tasks upon discharge, or with the assistance of family members.
- Signed informed consent by the patient or their family members.
You may not qualify if…
- Patients already enrolled in other stroke-related healthcare quality improvement projects or clinical trials.
- Patients or family members who refuse to sign the informed consent form.
- Pregnant or breastfeeding women.
Where it is running
- Beijing Tiantan Hospital — Beijing, China (enrolling)
- Beijing Tsinghua Changgung Hospital — Beijing, Beijing Municipality, China
- The First Affiliated Hospital of Shihezi University — Shihezi, Xinjiang, China
Full record on ClinicalTrials.gov
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