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

31 de agosto de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

26000

Fase

  • No aplica

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Comparador activo: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
3-Year Cumulative Incidence of First-Ever Ischemic Stroke
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cumulative Incidence of First-Ever Transient Ischemic Attack
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

31 de agosto de 2026

Finalización primaria (Estimado)

31 de diciembre de 2029

Finalización del estudio (Estimado)

31 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

18 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

18 de agosto de 2026

Publicado por primera vez (Actual)

21 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

31 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • AI-ExpoStroke-001
  • 2026-2G-20111 (Otro número de subvención/financiamiento: Capital's Funds for Health Improvement and Research)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan 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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .