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AI-Driven Health Management to Prevent Ischemic Stroke in High-Risk Adults (AI-ExpoStroke)

31 août 2026 mis à jour par: Xuanwu Hospital, Beijing

Intelligent Early Warning of Ischemic Cerebrovascular Disease Based on Multi-Source Data Fusion and Demonstration of Tiered Prevention and Control in Beijing

This study will evaluate whether an artificial intelligence (AI)-driven dynamic health management strategy can help prevent ischemic stroke in adults at high risk of stroke. Participants will be identified through community-based screening in Beijing using the AI-ExpoStroke model together with established stroke risk factors.

Communities will be randomly assigned to either an AI-driven health management group or a usual community-based health management group. Participants in the AI-driven group will receive continuous health management supported by a digital platform, mobile applications or WeChat-based tools, wearable-device data when available, personalized health guidance, and remote support from community health care providers. Participants in the usual-care group will receive routine community health services, including health examinations, health education, chronic disease follow-up, and medication guidance.

Participants will be followed for 36 months. The main goal is to determine whether AI-driven health management reduces the occurrence of first-ever ischemic stroke. The study will also evaluate transient ischemic attacks, stroke-related disability, mortality, control of major vascular risk factors, adherence to health management, and health economic outcomes.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Description détaillée

This is an investigator-initiated, multicenter, open-label, stratified cluster-randomized, parallel-group clinical study conducted in community settings in Beijing, China. The study is designed to evaluate the effectiveness, safety, and health economic value of an AI-driven dynamic health management strategy for the primary prevention of ischemic stroke in adults identified as being at high risk of stroke.

Potential participants will be identified from prospective community-based screening programs. Eligibility will be determined using the AI-ExpoStroke risk assessment model together with established stroke "8+2" high-risk factors. The AI-ExpoStroke model was developed and externally validated as part of preceding observational research and is used in the present interventional study primarily for identification and enrollment of individuals at high risk of stroke.

Randomization will be performed at the community level rather than at the individual participant level. Communities will be stratified according to area type, baseline risk-factor profile, and community health service resources, and will then be randomly assigned in a 1:1 ratio to the intervention group or control group. The random allocation sequence will be generated by an independent statistician using SAS or R. Because of the nature of the intervention, the study is open label.

Participants in the intervention group will receive AI-driven remote follow-up and continuous dynamic health management through a stroke prevention and management cloud platform, mobile applications or WeChat-based tools, wearable-device interfaces when applicable, and coordinated support from community health care providers. Participants will generally be encouraged to report health information such as blood pressure, body weight, medication use, and lifestyle-related information at least monthly. The platform will provide individualized risk-management targets, health reminders, lifestyle recommendations, and remote guidance from community health care providers. AI-generated recommendations will be used as supportive management tools and will not replace routine clinical decision-making by physicians.

Participants in the control group will receive usual community-based health management for individuals at high risk of stroke. This includes routine health examinations, basic health education, standard chronic disease follow-up, and medication guidance. Participants in the control group will not receive the dynamic AI-based management service.

All participants will be followed for 36 months, with formal follow-up assessments at 12, 24, and 36 months. Suspected stroke, transient ischemic attack, hospitalization, and death will be evaluated when they occur. Endpoint events will be verified using relevant clinical information and, when applicable, neuroimaging findings and medical records according to a predefined endpoint adjudication process.

The primary objective is to determine whether AI-driven dynamic health management reduces the 3-year cumulative incidence of first-ever ischemic stroke compared with usual community-based health management. Secondary evaluations include transient ischemic attack, stroke-related disability, mortality, vascular risk-factor control, adherence to intervention and follow-up, improvement in stroke-prevention knowledge, and health economic outcomes.

The study does not involve an investigational drug, an invasive investigational device, or collection of additional research-specific biological samples. Laboratory and clinical information used in the study will primarily be obtained from examinations performed as part of routine clinical care, routine physical examinations, or standard community health management.

Type d'étude

Interventionnel

Inscription (Estimé)

26000

Phase

  • N'est pas applicable

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Age 30 years or older, with no restriction on sex.
  • Permanent resident of Beijing.
  • No previously diagnosed stroke based on prospective community screening.
  • Identified as being at high risk of stroke by the AI-ExpoStroke model in combination with the established stroke "8+2" high-risk factors.
  • Able to comply with study follow-up and willing to provide informed consent.

Exclusion Criteria:

  • Previous diagnosis of ischemic stroke or hemorrhagic stroke.
  • Severe cognitive impairment.
  • Severe organic disease, including malignant tumors, New York Heart Association (NYHA) class III or higher heart failure, renal failure, or other severe conditions.
  • Psychiatric or language impairment that prevents completion of study questionnaires or follow-up.
  • Inability to obtain complete follow-up data or unwillingness to permit access to relevant study data.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Arm 1
AI-Driven Dynamic Health Management
A comprehensive AI-supported health management strategy for adults at high risk of stroke. The intervention integrates the AI-ExpoStroke risk assessment system with a digital stroke prevention and management platform, mobile applications or WeChat-based tools, wearable-device interfaces when applicable, and coordinated community health care. Participants generally report blood pressure, body weight, medication use, and lifestyle-related information at least monthly. The platform supports dynamic risk assessment, individualized risk-factor management targets, health reminders, lifestyle recommendations, health education, and remote guidance from community health care providers. AI-generated recommendations are intended to support health management and do not replace clinical decision-making by physicians.
Comparateur actif: Arm 2
Usual Community-Based Health Management
Usual community-based health management for adults at high risk of stroke, including routine health examinations, basic health education, standard chronic disease follow-up, and routine medication guidance according to community health care practice. Participants do not receive the AI-driven dynamic health management service provided through the AI-ExpoStroke platform.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
3-Year Cumulative Incidence of First-Ever Ischemic Stroke
Délai: From randomization through 36 months
The proportion of participants who experience a first-ever ischemic stroke during the 36-month follow-up period. Ischemic stroke will be confirmed based on clinical symptoms and signs together with neuroimaging evidence, including computed tomography or magnetic resonance imaging, according to the predefined endpoint adjudication process.
From randomization through 36 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Cumulative Incidence of First-Ever Transient Ischemic Attack
Délai: From randomization through 36 months
The proportion of participants who experience a first-ever transient ischemic attack (TIA) during the follow-up period, based on clinical evaluation and relevant medical records according to the predefined endpoint adjudication process.
From randomization through 36 months
Proportion of Participants With Disability Following Incident Stroke
Délai: From randomization through 36 months
The proportion of participants with an incident stroke who are assessed as having stroke-related disability during follow-up. Disability status will be evaluated at endpoint assessment, and the modified Rankin Scale (mRS) will be recorded for participants with stroke-related disability.
From randomization through 36 months
All-Cause Mortality
Délai: From randomization through 36 months
The proportion of participants who die from any cause during the 36-month follow-up period. Deaths will be verified using available medical records, discharge summaries, death certificates, or other relevant records.
From randomization through 36 months
Cardiovascular and Cerebrovascular Mortality
Délai: From randomization through 36 months
The proportion of participants who die from cardiovascular or cerebrovascular causes during the 36-month follow-up period. Cause of death will be determined using available clinical records and the predefined endpoint adjudication process.
From randomization through 36 months
Proportion of Participants Achieving Blood Pressure Control
Délai: At 12, 24, and 36 months
The proportion of participants who meet the predefined blood pressure control target at follow-up assessments.
At 12, 24, and 36 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

31 août 2026

Achèvement primaire (Estimé)

31 décembre 2029

Achèvement de l'étude (Estimé)

31 décembre 2029

Dates d'inscription aux études

Première soumission

18 août 2026

Première soumission répondant aux critères de contrôle qualité

18 août 2026

Première publication (Réel)

21 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

2 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

31 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • AI-ExpoStroke-001
  • 2026-2G-20111 (Autre subvention/numéro de financement: Capital's Funds for Health Improvement and Research)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual participant data will not be shared publicly because the study involves sensitive health information collected from a large community-based population. Study data will be de-identified, securely stored, and accessed only by authorized study personnel in accordance with the approved study protocol, institutional ethics requirements, and applicable data protection regulations. Aggregate study results may be disseminated through scientific publications and reports.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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