StroCare - Optimised Cross-sectoral,Coordinated Treatment of Stroke Patients With Patient-orientated Outcome Measurement

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.

Conditions

• Stroke

Interventions

OTHER

optimized cross-sectoral, structured and coordinated treatment pathway that integrates a patient-centred outcome evaluation

the optimized treatment pathway includes coordinated transitions between rehabilitation phases and institutes using individual case management and portal solutions

Sponsors & Collaborators

• Albertinen Krankenhaus

  collaborator OTHER

• Elbe Kliniken Stade-Buxtehude GmbH

  collaborator UNKNOWN

• Reha Centrum Hamburg GmbH

  collaborator UNKNOWN

• Klinikum Bad Bramstedt GmbH

  collaborator UNKNOWN

• MediClin Klinikum Soltau GmbH

  collaborator UNKNOWN

• VAMED Klinik Geesthacht

  collaborator UNKNOWN

• VAMED Rehaklinik Damp

  collaborator UNKNOWN

• BARMER Krankenkasse

  collaborator UNKNOWN

• Lohmann und Birkner medizinisches ServiceCenter GmbH

  collaborator UNKNOWN

• Forcare GmbH

  collaborator OTHER

• Universitätsklinikum Hamburg-Eppendorf

  lead OTHER

Principal Investigators

• Götz Thomalla, Prof. Dr. · University Medical Centre Hamburg-Eppendorf

Study Design

Allocation

NON_RANDOMIZED

Purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Model

SEQUENTIAL

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2020-01-01

Primary Completion

2023-12-05

Completion

2023-12-05

Countries

• Germany

Study Locations