Stroke
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age>=18, male or female; 2.Acute ischaemic stroke patient onsetted within 2 weeks; 3.CT scan or MRI confirmed fulfilled diagnostic criteria within 2 weeks; 4.Local civilian lived 6 months and beyond; 5.patients whom, willing to enter for the trial, high compliance and available to sign for the informed consent; 6.purchase with smart phone or other intelligent devices. Participants could only be included if they followed all criterias at the same time.
Exclusion criteria
Exclusion criteria: 1.Female individuals in gestation or breastfeeding period, or possitive result of pregnancy test before cluster randomization; 2.Patient accepting psychiatric or mental treatment that might pollut the result; 3.Life expectancy less than one year (e.g. complicated with malignant tumour, severe cardiac or pulmonary diseases); 4.Participant in other intervention studies that might interfere the result; 5.Investigators belief that patient is not suitable for this trial, or other situations that might have significant threat to the patient (e.g. cognitive impairment that could not understand and/or obey the programme and/or follow-up). The patient would be excluded if any one of these criteria have been attached.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Qualified rate of 90 days' systolic blood pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Relapse of stroke in 90 days;Compliance monitor of drug usage;Ability status post disease;Life quality;Knowledgement degree of secondary prevention against risk factor;Other relative index of stroke risk factor; | — |
Countries
China
Contacts
Xuanwu Hospital Capital Medical University