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Outcome after neurorehabilitative treatment of stroke: Comparative observational study in Germany and Kazakhstan.

Outcome after neurorehabilitative treatment of stroke: Comparative observational study in Germany and Kazakhstan.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033827
Enrollment
90
Registered
2024-04-22
Start date
2024-04-24
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

I60 I61 I63 I64

Interventions

Group 1: 90 patients after stroke in Germany. Within the framework of inpatient neurorehabilitation, patient information is systematically collected at the beginning and end of the stay. The data coll
2. After two weeks of inpatient neurorehabilitation
3. Three months post-event
4. Six months post-event. The assessments based on the ICF model and interim histories are consistent across all four appointments, except that the questionnaire on quality of life, the "Stroke Speci
10-meter walk test (maximum and comfortable walking speed)
Functional Ambulation Categories (FAC)
Action Research Arm Test (ARAT) and Barthel Index (BI)
cognition with the Montreal Cognitive Assessment (MoCA)
depression with the Hospital Anxiety and

Sponsors

Lurija Institut Kliniken Schmieder Allensbach
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - First stroke - Time since the event: 40 and = 70 at study inclusion - Ability to understand basic instructions and information - Willingness to participate by the patient or their carer - Knowledge of the type of stroke (ischaemic / haemorrhagic)

Exclusion criteria

Exclusion criteria: - Presence of a serious, life-shortening other illness (e.g. cancer, severe heart failure, severe lung disease) - Presence of a severe psychiatric illness - Presence of other neurological diseases - Pain during physical activity (visual analogue scale > 5) - Gastric tube, percutaneous endoscopic gastrostomy

Design outcomes

Primary

MeasureTime frame
Assessments based on the International Classification of Functioning, Disability and Health (ICF): 6-minute walk test (6MinWT); 10-meter walk test (maximum and comfortable walking speed); Berg Balance Scale; Functional Ambulation Categories (FAC); Action Research Arm Test (ARAT) and Bartel Index (BI)

Secondary

MeasureTime frame
Assessments based on the International Classification of Functioning, Disability and Health (ICF): Cognition with Montreal Cognitive Assessment (MoCA); depression with the Hospital Anxiety and Depression Scale (HADS); Stroke Specific Quality of Life Scale (SS-QOL)and the number and type of therapies and complications.

Countries

Germany, Kazakhstan

Contacts

Public ContactJoachim Liepert

Kliniken Schmieder Allensbach

j.liepert@kliniken-schmieder.de+4975338080

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026