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Trial registered on ANZCTR
Registration number
ACTRN12608000018314
Ethics application status
Approved
Date submitted
10/01/2008
Date registered
14/01/2008
Date last updated
1/12/2015
Type of registration
Prospectively registered
Titles & IDs
Public title
Anticholinergic and sedative drug use and functional status among older Australians.
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Scientific title
Can medication review using the drug burden index improve function in older Australians?
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Secondary ID [1]
507
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None.
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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:
Medication exposure in older adults.
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Physical and cognitive functioning in older adults.
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Condition category
Condition code
Mental Health
2814
2814
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0
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Studies of normal psychology, cognitive function and behaviour
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Musculoskeletal
2815
2815
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0
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Normal musculoskeletal and cartilage development and function
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Public Health
2816
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0
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Health promotion/education
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Drug burden index is a tool used to quantify a person’s total exposure to anticholinergic and sedative medications. Drug burden index has been associated with physical and cognitive performance in older people. Drug burden index can be used to assess the risks and benefits of prescribing for older populations.
This project aims to test the validity of the drug burden index and its association with functional outcomes in an Australian population of older people living in retirement villages. It will also assess the feasibility of drug burden index as a prompt for medication review.
The intervention will be conducted over 3 months and it will involve prompting General Practitioners to reduce those drugs contributing to drug burden index and potentially impairing the patient’s physical and cognitive function.
For the intervention group, a report including list of medications associated with drug burden index will be sent to the General Practitioner for consideration of possible withdrawal (dose reduction or cessation). The report will quantify the degree of functional impairment that may be associated with the participant's drug burden.
For the control group, there will be no prompting about drug burden.
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Intervention code [1]
2433
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Treatment: Drugs
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Comparator / control treatment
The control treatment is active. The control group will receive standard care from their General Practitioners. There will be no prompting about drug burden.
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Control group
Active
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Outcomes
Primary outcome [1]
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Exposure to medications with anticholinergic and sedative effects using the drug burden index.
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Assessment method [1]
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Timepoint [1]
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At baseline and 3 months.
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Primary outcome [2]
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Objective measures of physical and cognitive function.
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Assessment method [2]
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Timepoint [2]
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At baseline and 3 months.
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Secondary outcome [1]
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General practitioners' reasons for prescribing or withdrawing medications with sedative or anticholinergic effects.
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Assessment method [1]
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Timepoint [1]
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After baseline interview.
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Eligibility
Key inclusion criteria
People aged > 70 years who consult their general practitioners regularly who live in the participating retirement villages in Sydney, Australia.
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Minimum age
70
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Unable to obtain informed consent from resident or legal caregiver.
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Study design
Purpose of the study
Educational / counselling / training
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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)
Allocation is not concealed.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Method of randomisation: Stratified allocation by centre.
Retirement villages will be randomised as intervention and control sites.
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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
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Phase
Not Applicable
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Type of endpoint/s
Safety/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
4/02/2008
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Actual
29/02/2008
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Date of last participant enrolment
Anticipated
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Actual
10/03/2009
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
150
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Accrual to date
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Final
115
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
719
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2060
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Recruitment postcode(s) [2]
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2089
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Geoff & Elaine Penney Aged Care Trust Fund
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Address [1]
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Aged Care & Rehabilitation Department
Royal North Shore Hospital
Pacific Highway, St Leonards, NSW 2065
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Country [1]
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Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Geoff & Elaine Penney Aged Care Trust Fund
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Address
Aged Care & Rehabilitation Department
Royal North Shore Hospital
Pacific Highway, St Leonards, NSW 2065
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
2660
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Northern Sydney Health Human Research Ethics Committee (Harbour)
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Ethics committee address [1]
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The Research Office, Level 4, Vindin House Royal North Shore Hospital St Leonards NSW 2065
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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13/12/2007
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Ethics approval number [1]
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EC00333
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Summary
Brief summary
The proposed study will provide important insight for identifying medications that may contribute to functional impairments and age related disability in older Australians. This study aims to describe the exposure of older Australians to medications with sedative and anticholinergic effects using the Drug Burden Index. It will investigate the role of the drug burden index as a tool to guide prescribing in older Australians and whether changes drug burden are associated with changes in the physical and cognitive functional status.
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Trial website
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Trial related presentations / publications
The data will be used to write PhD thesis and will be presented through oral presentations at the University of Sydney and Royal North Shore Hospital. Results may be published in medical journals and presented at scientific and medical conferences.
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Public notes
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Contacts
Principal investigator
Name
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Prof Sarah Hilmer
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Address
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Level 12 Kolling Building
Royal North Shore Hospital and Kolling Medical Institute
St Leonards NSW 2065
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Country
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Australia
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Phone
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61 9926 4481
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Sarah Hilmer
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Address
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Clinical Pharmacology Department
11C Main Building RNSH
Pacific Highway, St Leonards, NSW 2065
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Country
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Australia
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Phone
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+61 2 9926 7631
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Fax
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+61 2 9926 7614
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Sarah Hilmer
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Address
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Clinical Pharmacology Department
11C Main Building RNSH
Pacific Highway, St Leonards, NSW 2065
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Country
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Australia
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Phone
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+61 2 9926 7631
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Fax
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+61 2 9926 7614
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Email
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[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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