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Feasibility of a mobil, digital and sensor-based technology for secondary prevention, health competence and self-determination in combination with personal assistance after stroke

Feasibility of a mobil, digital and sensor-based technology for secondary prevention, health competence and self-determination in combination with personal assistance after stroke - PostStroke-Manager

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00023213
Enrollment
90
Registered
2021-04-27
Start date
2021-06-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke I64

Interventions

Group 1: Combination of a mobile, digital system and personal assistance after stroke

Sponsors

Universität Leipzig, Medizinische Fakultät,Klinik und Poliklinik für Neurologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - age > 18 years - written informed consent or verbal consent among witnesses - pre-mRS 0-2 i.e. at most minor impairment before the event - stable course of stroke or TIA-related clinical and paraclinical parameters, so that discharge from the hospital is possible - possibility of operation of the digital system and use of the communication elements by the patient (critical parameters are considered to be the presence of a severe neglect or a high degree of hemiparesis or a severe aphasic disorder that does not enable communication) - residence in the Leipzig area - consent of the treating general practitioner to participate in the study

Exclusion criteria

Exclusion criteria: - other illness of competing severity that makes study participation as intended impossible (e.g cancer with a life expectancy of less than one year) - recognizable inability to use the study-related software or end devices - presence of a chronic, clinically relevant psychiatric disease before the cerebrovascular event - pre-existing dementia - existing qualitative or quantitative disturbance of consciousness - patients who cannot be followed for one year - existing or planned pregnancy

Design outcomes

Primary

MeasureTime frame
The feasibility of the support system under “real-life” conditions should be evaluated by the participants with an integrated questionnaire at the end of the observation period. The questionnaire contains the assessment of the digital and personal support and also of the corresponding digital single modules. The assessment follows a six-stage scale from “very large support” to “no support”. In addition to that, the patients receive the possibility to formulate their suggestions and desires how to improve the support system as a free text. The system should be evaluated as “feasible”, if at least 50% of the single modules are positively rated by at least 75% of the participants.

Secondary

MeasureTime frame
An unstructured feedback of stroke pilots, general and other practitioners about the feasibility of the support system should help to develop the content and the technical specifications further. Descriptive analyses of the course of psychometric variables, vital parameters, physical limitations and laboratory parameters are intended to provide an insight into the long-term course of the stroke disease. A stratification concerning the diagnostic groups cerebral infarction, cerebral haemorrhage and TIA could help to identify patients with post-hoc analyses, which would have a particularly benefit from the support system. Biomedical analyses of the terminal devices data should form the basis for further and new developments of modern interpretation possibilities of non-invasively available bio signals. In addition, technical analyses of usage behavior and problems encountered in dealing with the use of the digital system are of great importance for the further development of the system.

Countries

Germany

Contacts

Public ContactDominik Michalski

Universität Leipzig, Medizinische Fakultät,Klinik und Poliklinik für Neurologie

dominik.michalski@medizin.uni-leipzig.de0341-9724339

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 21, 2026