Clinical trials

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Condition / disease
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Status: Not yet recruiting

Digital Application for Stroke Health

Stroke is a leading cause of death and long-term disability worldwide. Despite substantial advances in acute stroke care, there remains a lack of evidence-based digital solutions to support patients after hospital discharge. This study evaluates the effectiveness of a digital health application (StrokeApp) designed to support patients with ischemic or hemorrhagic stroke or transient ischemic attack (TIA) in secondary prevention and recovery. In this multicenter, randomized, controlled, open-label trial, 500 patients will be assigned in a 1:1 ratio to receive either standard care alone or standard care in combination with StrokeApp. The primary objective is to assess the impact of the application on health-related quality of life three months after discharge. Secondary and exploratory outcomes include health literacy, medication adherence, vascular risk factors, health-related behaviors, psychosocial outcomes, long-term recovery up to twelve months, as well as safety and user experience.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VASCage GmbHUpdated: Apr 6, 2026Locations: 7
Eligibility criteria

Male or female patient (biological sex) ≥18 years at the time of consent [+3]

Cerebral infarction due to cerebral venous thrombosis (CVT) [+14]

Status: Recruiting

Exploratory Study on the Potential Cross-System Effects of BCI-FES Hand Therapy on Dysphagia and Aphasia in Chronic Stroke Patients

The goal of this neurorehabilitation explorative study is to investigate how a closed-loop Brain-Computer Interface Functional Electrical Stimulation (BCI-FES) therapy, used within the intended purpose for hand rehabilitation, may impact swallowing difficulties (dysphagia) and language disorders (aphasia) in post-stroke patients.

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VASCage GmbHUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Age: Participants must be aged 18 years or older. [+9]

Cognitive Impairments: Cognitive impairments that, in the investigator's judgmen... [+19]

Status: Recruiting

Innsbruck Health Promotion Program

The primary goal of this single-centre. single-arm, unblinded, pre-post interventional study is to evaluate whether a one-time health assessment and intervention affects the overall vascular health evaluated through the Life's Essential 8 overall vascular health score. Secondary goals of this study are, among others: * to describe incidence and prevalence of vascular risk-factors and behaviours * to explore prevalence and associations of health and disease in the general population with special focus on cardiovascular risk, cardiovascular diseases, markers of vascular health, signs and (prodromal) symptoms of neurodegeneration as well as psychosocial factors * to explore the prevalence of hearing disorders in the general population * to collect voice and speech samples to identify novel biomarkers that correlate to vascular health and/or hearing status

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VASCage GmbHUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

Signed informed consent of subject [+1]

People who are suspended upon a court order or upon other legal processes or are... [+2]

Status: Recruiting

Stroke-Card Registry

Stroke is the second leading cause of death and one of the main contributors to disability. Patients who survive the acute phase of ischemic stroke and those with transient ischemic attack (TIA) are at high risk of subsequent vascular events. Importantly, recurrent strokes are associated with a higher social and economic impact, higher case fatality, and worse clinical outcome than first-ever strokes. The burden of post-stroke complications, residual deficits, and inadequate medical and psychosocial care all contribute to long-term disability and reduced quality of life in these patients. The Department of Neurology of the Medical University Innsbruck undertook the STROKE-CARD trial (NCT02156778) between 2014 and 2018 with follow-up until 2019 to evaluate the efficacy of the Post-Stroke disease-management program STROKE-CARD care. After implementation of STROKE-CARD care, the investigators aim to document the quality of post-stroke care and compare outcome parameters to historical cohorts and the change over time. Furthermore the investigators aim to gain a large data-resource for future research of biomarkers, disease mechanisms, prognosis and imaging mechanisms for R\&D.

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: VASCage GmbHUpdated: Mar 5, 2025Locations: 2Duration: 7 Years
Eligibility criteria

Patients with acute ischemic stroke or high-risk TIA (ABCD2-Score ≥ 4 points) tr... [+2]

Patients living outside the catchment area of the participating centers [+2]