About this trial
This study was designed to evaluate the impact of non-pharmacological multimodal interventions including ongoing orientation, sensory correction, setting of familiar circumstance and promotion of sleep enviromnet for prevention of delirium in intensive care unit.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients over 50 years who are expected to spend more than 24 hours in the intensive care unit
Disqualifiers
Patients who developed delirium before entering the intensive care unit
Patients with cognitive impairment
Patients who have hearing or vision deficits, or have difficulty in communication
Patients who are expected to die within 24 hours or do not want life-sustaining treatment
Trial design
Parallel
Treatments tested in this trial
Multimodal therapy for prevention of delirium
Other interventionMultimodal therapy for prevention of delirium
Treatment groups
Trial outcomes
Primary outcomes
Number of patients with delirium
Delirium assessed by Confusion Assessment Method for the ICU (CAM-ICU)
Secondary outcomes
Delirium-free days
Delirium assessed by Confusion Assessment Method for the ICU (CAM-ICU)
Severity of delirium
Confusion Assessment Method for the ICU-7 (CAM-ICU-7) delirium severity score
Accidental extubation or disconnection of treatment devices
Accidental extubation or disconnection of treatment devices
ICU and hospital length of stay
Duration of ICU and hospital stay
Sponsors and contacts
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