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Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors

Delirium Clinical Trial

Official title:
Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors (DANE)

Clinical Trial Summary

This study will evaluate the usefulness of the Emergency General Surgery (EGS) Delirium Recovery Model. It is hypothesized that the cognitive, physical and psychological recovery of older EGS delirium survivors will be improved through the use of the EGS Delirium Recovery Model. Participants can expect to be on the study for 18 months.

Clinical Trial Description

This is a multi-site, two-arm, single-blinded randomized controlled clinical trial to evaluate the efficacy of the EGS Delirium Recovery Model to improve the cognitive, physical and psychological recovery of older EGS delirium survivors. At or near the time of discharge, enrolled participants will be randomized to receive the EGS-Delirium Recovery Model or usual care. The hypothesis is that, after 18 months, older EGS delirium survivors who are randomized to the EGS Delirium Recovery Model will experience more favorable cognitive, physical and psychological recovery in comparison to those randomized to usual care. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05373017
Study type Interventional
Source University of Wisconsin, Madison
Contact Sarah Robbins
Phone 608-265-9138
Email robbins@surgery.wisc.edu
Status Recruiting
Phase N/A
Start date February 13, 2023
Completion date January 31, 2028
View Details
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