Structured outpatient aftercare after stroke (SANO) - extended post-interventional follow-up

Conditions: I64
Stroke, not specified as haemorrhage or infarction

Registration Number: DRKS00033430

Lead Sponsor: Institut für Klinische Epidemiologie und Biometrie (IKE-B) der Universität Würzburg

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: All

Target Recruitment: 1654

Inclusion Criteria

Patients who have participated in the SANO study and who have given their consent to the extended follow-up survey.
Patient understands the contents of the study and can make the decision to participate in the study independently.

Exclusion Criteria

none

Study & Design

Study Type: observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Combined endpoint of recurrent stroke, myocardial infarction or death within five to six years after stroke

Secondary Outcome Measures

Name	Time	Method
Rate of individual components of the primary endpoint<br>Rate of transient ischemic attacks (TIAs) within five to six years after stroke<br>Control of cardiovascular risk factors according to predefined targets based on clinical guidelines<br>Functional outcome (mRS) after five to six years <br>Drug treatment including prescription of antiplatelet or anticoagulant drugs<br>Rate of readmission to hospital after five to six years <br>Adequate provision of assistive devices and therapies<br>Quality of life reported by patients (European Quality of Life 5 Dimensions (EQ-5D) and Patient Reported Outcomes Measurement Information System (PROMIS 29))<br>Rate of complications (cognitive impairment, depression and anxiety, fatigue, falls, etc.) and their guideline-compliant treatment