Delirium in Old Age Clinical Trial
Official title:
Cognitive Stimulation Guided by a Software to Prevent Delirium in Older Patients
This study is a pilot randomized controlled trial, comparing a group of older patients with
standardized non-pharmacological delirium prevention plus a basic tablet versus a group with
standardized non-pharmacological delirium prevention plus a tablet with a software of
cognitive stimulation (PREVEDEL).
Software:It is a local development, including a interprofessional team of delirium healthcare
experts, older patients and a team og engineers. The software was developed during the first
year of this project and was inscribed for author rights.
Inclusion criteria: Older patients > 65 y.o. Admitted to medicine room or intermediate care
unit > 48 hrs, and informed consent to participate.
Exclusion Criteria:Delirium positive, neuroleptic use, dementia, and non-spanish speakers.
The study was approved by ethical committee of Hospital Clinico University of Chile
Standardized Non-pharmacological intervention: Health workers were previously educated in
delirium, and environmental issues were implemented. This intervention coverage in nine
different domains: orientation, early mobilization, environmental noise and light, sensorial
deficit, sleep, hydratation, drug reduction, and family participation.
Intervention: All patients will have a tablet with or without the software PREVEDEL between
09:00-19:00 hrs.
Measures: delirium will be monitoring with CAM (Confusion Assessment Method) twice a day for
5 days.
Primary outcome: Delirium rate between both groups Secondary outcomes:Long of stay, severity
od delirium, time of use of electronic device, and Barthel to discharge.
n/a
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