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Clinical Trial Summary

An investigator-initiated, evaluator-blinded, prospective, multi centre, before-and-after, effectiveness-implementation hybrid design study to assess the feasibility of essential acute stroke care in a low resource setting


Clinical Trial Description

This is a multicentre, before and after, effectiveness-implementation hybrid study design with blinded outcome assessment. Patients admitted to the participating hospitals will be managed under usual care conditions for three months (control arm). This will be followed by the training of the doctors and nurses in those hospitals on essential acute stroke care management. Patient management for the following three months after the training (intervention) will then be assessed to evaluate its impact on the care and clinical outcome of the patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04157231
Study type Interventional
Source The George Institute
Contact Cheryl Carcel, Dr
Phone +61 2 8052 4508
Email ccarcel@georgeinstitute.org.au
Status Not yet recruiting
Phase N/A
Start date October 30, 2024
Completion date November 30, 2025

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