StroCare - Optimised Cross-sectoral,Coordinated Treatment of Stroke Patients With Patient-orienta… (NCT04159324) | Clinical Trial Compass
CompletedNot Applicable
StroCare - Optimised Cross-sectoral,Coordinated Treatment of Stroke Patients With Patient-orientated Outcome Measurement
Germany409 participantsStarted 2020-01-01
Plain-language summary
The Trial is a multi-centred controlled interventional study with a pre-post design. The primary aim of the study is the evaluation of the effectiveness and cost-effectiveness of the StroCare treatment.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients in inpatient care in the stroke unit of one of the participating acute clinics who are insured at the BARMER health insurance agency with the following diagnosis (ICD-10):
* Ischemic attack (I63)
* Transient ischemic attack and related syndromes (G45)
* Intracerebral haermorrhage (I64)
* Written informed consent
* Sufficient mastery of German language
Exclusion Criteria:
* Substantially impaired communication capacity due to aphasia or dementia
* Patients with artificial Respiration
* Insufficient adherence
* Premorbid score of mRS≥4
* Patients with artificial Respiration (Z99.1)
* Dementia (F00.x., F01.x. or G30.x) or aphasia (R47)
* Death during inpatient Treatment or the Admission to a nursing home following the acute treatment