Does an enhanced exercise and cognitive program reduce incident delirium?

Completed

• Conditions: Delirium; Neurological - Other neurological disorders

• Registration Number: ACTRN12605000044628
• Lead Sponsor: orthern Clinical Research Centre

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-07-26
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 900

Inclusion Criteria

Hospital inpatient under a medical bed card in the trial area.

Exclusion Criteria

Severe dysphasia, death expected within 24 hours, infectious isolation, documented contraindication to mobilisation, admission to the stroke or critical care unit, planned admission of less than 48 hours, major psychiatric diagnosis, admission for known delirium, admission from another hospital, previous inclusion in the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ew onset of delirium in hospital.[assessed every 48 hours during weekdays]

Secondary Outcome Measures

Name	Time	Method
Functional status[assessed every 48 hours during weekdays];Discharge destination[At hospital discharge];Length of stay[At hospital discharge]