- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06816238
Smart Education for MACE Prevention and Early Detection (SEED)
Smart Education for Major Adverse Cardiovascular Events Prevention and Early Detection
With its high incidence, recurrence, disability, and mortality, stroke has become a significant health challenge in society today. However, "stroke can be prevented and treated," and high-risk groups for stroke are the primary beneficiaries of stroke prevention and control measures. Yet, these populations often have low awareness of proper stroke prevention and treatment knowledge. The reasons for this may include limited coverage, lack of accessibility, inadequate relevance, and uneven content quality in traditional health education measures.
To address these issues, innovative intervention strategies are needed to explore more effective health education methods. The occurrence of Major Adverse Cardiovascular Events (MACE), such as stroke, can be reduced by improving the knowledge and practical abilities of high-risk populations regarding scientific stroke prevention and treatment. One such strategy is the use of smartphone-based information software, which can break the constraints of time and space, delivering health education knowledge to a broader audience. To enhance accessibility, key knowledge points can be repeatedly delivered to the target population through one-way push notifications and interactive Q&A, allowing for more engaging and flexible learning. In terms of improving pertinence, it is essential to tailor health education delivery to the individual needs of the educatees, considering factors such as age, education level, and risk factors. Furthermore, the quality of health education content must be authoritative, scientifically accurate, easy to understand, and practically applicable. The content should be based on the latest scientific research and professional medical practice, reviewed by authoritative institutions or experts, and should align with the needs of the educated populations for self-health management. Additionally, human and financial costs should be considered when designing such interventions.
In this study, a large-scale medical model based on a stroke prevention and treatment knowledge base, integrated with an intelligent medical system and interactive Q&A, is employed. This approach ensures content quality while minimizing the need for additional manpower in education and Q&A, making the intervention more cost-effective and scalable for widespread use. The purpose of this study is to explore whether the incidence of MACE in a high-risk stroke population receiving interactive medical model education-based on a stroke prevention and treatment knowledge base-is lower than in a group without such interactive education.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
With its high incidence, recurrence, disability and mortality, stroke has become an important health challenge facing the society at present. However, "stroke can be prevented and treated," and high-risk groups of stroke are the main beneficiaries of stroke prevention and control and the intervention targets of "health education" measures. Yet, their awareness of correct stroke prevention and treatment knowledge is low. The reasons may be related to the limited coverage, lack of accessibility, lack of pertinence, and uneven content quality of traditional health education measures.
Therefore, we need to adopt innovative intervention strategies to overcome these constraints and explore effective ways of health education. The occurrence of Major Adverse Cardiovascular Events (MACE), such as stroke, can be reduced by improving the knowledge level and practical ability of scientific stroke prevention and treatment in high-risk populations. In this study, the intervention is based on a large medical model using a medical intelligent agent for interactive Q&A. This approach is designed to enhance popularization, accessibility, pertinence, and content quality.
Popularization: The use of smartphone-based information software can break through the limitations of time and space, conveying health education knowledge to a wider audience.
Accessibility: Key knowledge points can be repeatedly delivered to the target audience through one-way pushes of health education content, complemented by interactive Q&A with intelligent medical agents.
Pertinence: Health education content is personalized based on the individual's age, education level, risk factors, and other personal characteristics, ensuring relevance to each educatee.
Content Quality: The educational content is authoritative, scientifically accurate, easy to understand, and practical, drawing from the latest scientific research and professional medical practices, reviewed by authoritative experts and institutions. The intervention ensures that the educated's needs for self-health management are fully considered.
This model leverages the large medical knowledge base and intelligent medical agents to provide personalized, scalable, and cost-effective education, which eliminates the need for additional manpower in education and Q&A. This approach helps reduce costs while enabling large-scale implementation.
The purpose of this study was to explore whether the incidence of MACE in high-risk stroke populations receiving interactive education based on a medical knowledge model and intelligent Q&A is lower than that in a group without such education.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Individuals who meet the definition of a stroke risk group, including those with hypertension, dyslipidemia, diabetes, atrial fibrillation, valvular heart disease, a history of smoking, significant overweight or obesity, physical inactivity, a family history of stroke, or any combination of 8 or more stroke risk factors.
Individuals with a history of one or more transient ischemic attacks (TIAs) or a previous stroke.
Legal capacity to provide informed consent. Permanent residents of Zhejiang Province with Zhejiang Provincial household registration.
Ownership of a smartphone and access to the Alipay app. Voluntary participation and adherence to the principles of informed consent.
Exclusion Criteria:
Illiteracy or difficulty with reading/communication. Medical personnel. Inability to complete the study questionnaire due to physical or cognitive limitations.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
High-risk stroke population receiving interactive education based on a medical knowledge model, utilizing intelligent medical agents and interactive Q&A.
The educational content will cover stroke prevention and treatment, tailored to individual risk factors and needs.
|
interactive education based on a medical knowledge model, utilizing intelligent medical agents and interactive Q&A
|
|
Active Comparator: Control Group
High-risk stroke population receiving traditional health education methods without the use of the interactive medical model and intelligent Q&A system.
|
traditional health education methods without the use of the interactive medical model and intelligent Q&A system
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
MACE Incidence
Time Frame: 1 year from enrollment
|
The occurrence of major adverse cardiovascular events (MACE), including stroke (ischemic or hemorrhagic), myocardial infarction, heart failure, or cardiovascular death, in participants over the 1-year follow-up period.
MACE is a composite outcome that captures the broad range of adverse cardiovascular events.
|
1 year from enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroke Incidence
Time Frame: 1 year from enrollment
|
The occurrence of new stroke events (ischemic or hemorrhagic) in participants during the 1-year follow-up period.
|
1 year from enrollment
|
|
Hospitalization Due to Cardiovascular Events
Time Frame: 1 year from enrollment
|
The number of hospital admissions related to cardiovascular events, including stroke, myocardial infarction, heart failure, or other significant cardiovascular conditions.
|
1 year from enrollment
|
|
Stroke Prevention and Treatment Knowledge
Time Frame: 1 year from enrollment
|
Participants' knowledge of stroke prevention and treatment, assessed via surveys or questionnaires.
|
1 year from enrollment
|
|
Blood Pressure Control
Time Frame: 1 year from enrollment
|
Proportion of participants maintaining blood pressure within recommended levels (e.g., <140/90 mmHg) as part of stroke and cardiovascular risk management.
|
1 year from enrollment
|
|
Physical Function and Quality of Life (QoL)
Time Frame: 1 year from enrollment
|
Assessment of physical function and overall quality of life, measured using standardized scales like the EQ-5D or the SF-36, to understand the impact of the intervention on the participant's daily living and wellbeing.
|
1 year from enrollment
|
|
Adherence to Stroke Prevention Medications
Time Frame: 1 year from enrollment
|
Proportion of participants adhering to prescribed medications (e.g., antihypertensives, antiplatelets) for stroke prevention, measured via self-reports or pharmacy refill data.
|
1 year from enrollment
|
|
Smoking Cessation (for smokers)
Time Frame: 1 year from enrollment
|
Proportion of smokers who quit smoking within 3 months of the intervention, as assessed by self-report and/or biochemical validation (e.g., carbon monoxide levels, cotinine levels).
|
1 year from enrollment
|
|
Weight Loss (for overweight participants)
Time Frame: 1 year from enrollment
|
Proportion of overweight participants who lose at least 5% of their body weight within 3 months, measured via weight records.
|
1 year from enrollment
|
|
Sense of First Aid for Stroke
Time Frame: 1 year from enrollment
|
Improvement in participants' knowledge and confidence in providing first aid in the event of a stroke, measured through a standardized questionnaire or skills assessment.
|
1 year from enrollment
|
|
Thrombolysis Use in Ischemic Stroke
Time Frame: 1 year from enrollment
|
Proportion of ischemic stroke patients who receive thrombolysis treatment (IV tPA or intra-arterial therapy) within the recommended time window.
|
1 year from enrollment
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SEED
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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