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Trial registered on ANZCTR
Registration number
ACTRN12605000044628
Ethics application status
Approved
Date submitted
25/07/2005
Date registered
26/07/2005
Date last updated
7/04/2008
Type of registration
Retrospectively registered
Titles & IDs
Public title
Does an enhanced exercise and cognitive program reduce incident delirium?
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Scientific title
Does an enhanced exercise and cognitive program reduce incident delirium?
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Delirium
110
0
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Condition category
Condition code
Neurological
129
129
0
0
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Other neurological disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Twice daily progressive exercise program and orientation protocol for the duration of hospital admission.
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Intervention code [1]
53
0
Prevention
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Comparator / control treatment
Usual ward care
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Control group
Active
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Outcomes
Primary outcome [1]
164
0
New onset of delirium in hospital.
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Assessment method [1]
164
0
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Timepoint [1]
164
0
assessed every 48 hours during weekdays
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Secondary outcome [1]
359
0
Functional status
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Assessment method [1]
359
0
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Timepoint [1]
359
0
assessed every 48 hours during weekdays
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Secondary outcome [2]
360
0
Discharge destination
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Assessment method [2]
360
0
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Timepoint [2]
360
0
At hospital discharge
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Secondary outcome [3]
361
0
Length of stay
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Assessment method [3]
361
0
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Timepoint [3]
361
0
At hospital discharge
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Eligibility
Key inclusion criteria
Hospital inpatient under a medical bed card in the trial area.
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Minimum age
65
Years
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Maximum age
N/A
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key 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.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
sealed envelopes opened by person unaware of patient details
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Each person is randomised to treatment group separately from a store of sealed envelopes (15 control, 15 intervention) which are replenished after each person is randomised. That is, the selection of treatment group occurs in much the same way as if a coin was tossed. There is no blocking or stratification.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
Control is usual hospital care
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
2/05/2005
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
900
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
178
0
Government body
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Name [1]
178
0
Northern Health
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Address [1]
178
0
185 Cooper St Epping VIC 3076
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Country [1]
178
0
Australia
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Funding source category [2]
179
0
Government body
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Name [2]
179
0
NHMRC
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Address [2]
179
0
GPO Box 1421 Canberra ACT 2601
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Country [2]
179
0
Australia
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Funding source category [3]
180
0
Charities/Societies/Foundations
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Name [3]
180
0
HCF Health and Medical Research Foundation
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Address [3]
180
0
GPO Box 4242 Sydney NSW 2001
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Country [3]
180
0
Australia
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Primary sponsor type
Hospital
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Name
Northern Clinical Research Centre
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Address
185 Cooper St Epping VIC 3076
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Country
Australia
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Secondary sponsor category [1]
134
0
None
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Name [1]
134
0
Not applicable
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Address [1]
134
0
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Country [1]
134
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
946
0
The Northern Hospital
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Ethics committee address [1]
946
0
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Ethics committee country [1]
946
0
Australia
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Date submitted for ethics approval [1]
946
0
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Approval date [1]
946
0
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Ethics approval number [1]
946
0
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Summary
Brief summary
This project aims to investigate the effects of additional exercise and a standardised orientation intervention on the development of delirium in hospital.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
35935
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Address
35935
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Country
35935
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Phone
35935
0
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Fax
35935
0
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Email
35935
0
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Contact person for public queries
Name
9242
0
Kim Jeffs
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Address
9242
0
Northern Clinical Research Centre
The Northern Hospital
185 Cooper St
Epping VIC 3076
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Country
9242
0
Australia
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Phone
9242
0
+61 3 84058804
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Fax
9242
0
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Email
9242
0
[email protected]
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Contact person for scientific queries
Name
170
0
Kim Jeffs
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Address
170
0
Northern Clinical Research Centre
The Northern Hospital
185 Cooper St
Epping VIC 3076
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Country
170
0
Australia
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Phone
170
0
+61 3 84058804
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Fax
170
0
+61 3 84058683
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Email
170
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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