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Trial registered on ANZCTR
Registration number
ACTRN12615000429550
Ethics application status
Approved
Date submitted
24/04/2015
Date registered
6/05/2015
Date last updated
6/05/2015
Type of registration
Retrospectively registered
Titles & IDs
Public title
Evaluation of patients’ warfarin knowledge and outcomes following secondary warfarin education (in an outpatient setting) compared with standard inpatient education, as measured by the Oral Anticoagulation Knowledge test.
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Scientific title
In patients newly commenced on warfarin for any indication, does additional outpatient education compared to standard inpatient education improve patients' knowledge of warfarin and anticoagulation control, as measured by the Oral Anticoagulation Knowledge (OAK) test and International Normalised Ratio (INR) control.
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Secondary ID [1]
286591
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Nil
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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:
Anticoagulation control - Warfarin education
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Condition category
Condition code
Public Health
295129
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0
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Health promotion/education
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Cardiovascular
295182
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0
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Diseases of the vasculature and circulation including the lymphatic system
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Patients receive a 1 hour education session delivered by the primary researchers, as an outpatient. This includes a powerpoint presentation and a worksheet covering the basics of warfarin - how it works, indications, its purpose, practicalities for taking warfarin and testing INR, frequency of INR testing, interactions with drugs and diet, and major side of effects of warfarin (including when to seek help). The session occurs within 2 weeks of the patient leaving hospital.
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
Patients receive standard inpatient warfarin education, which is usually delivered by a ward pharmacist and normally takes 15-20 minutes. This involves the basics of warfarin including why the patient is on warfarin, checking their INR, dietary interactions and when to seek help.
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Control group
Active
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Outcomes
Primary outcome [1]
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Oral Anticoagulation Knowledge (OAK) Test, a validated 20 question multiple choice test for assessing patients' knowledge of warfarin.
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Assessment method [1]
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Timepoint [1]
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Administered 6 weeks post discharge from hospital
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Secondary outcome [1]
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Patients' International Normalised Ratio (INR) control, as measured by Time in Therapeutic Range.
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Assessment method [1]
314293
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Timepoint [1]
314293
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INR data was gathered from the time of discharge up to 2 months post discharge from hospital.
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Eligibility
Key inclusion criteria
1. Newly commenced on warfarin (any indication)
2. Inpatient at Royal Melbourne Hospital
3. Age greater than or equal to 18 years old
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Minimum age
18
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?
No
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Key exclusion criteria
1. Duration of warfarin therapy <6 weeks
2. Non English speaking background with no available family translator
3. Prior warfarin therapy
4. Pregnancy
5. Moderate to severe cognitive impairment, defined as an Abbreviated Mental Test Score (AMTS) of 6 or less
6. Discharged to residential or nursing care, as warfarin was unlikely to be self-managed
7. Health professionals with prior knowledge of warfarin
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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)
Randomisation schedule is generated in code (in SPSS, by a third party) prior to recruitment and held by a blinded third party. Allocation involves contacting the holder of the randomisation schedule who is “off-site”.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people analysing the results/data
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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
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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
1/02/2014
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Actual
10/02/2014
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Date of last participant enrolment
Anticipated
1/06/2014
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Actual
27/08/2014
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Royal Melbourne Hospital - City campus - Parkville
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Shireen Bhatt
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Address [1]
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9 Mercantile Parade,
Kensington
VIC 3031
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Country [1]
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Australia
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Funding source category [2]
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Self funded/Unfunded
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Name [2]
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Claire McCurdy
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Address [2]
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19/8-10 Martin St
Thornbury
VIC 3071
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Country [2]
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Australia
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Primary sponsor type
Hospital
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Name
Royal Melbourne Hospital
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Address
300 Grattan Street
Parkville
VIC 3050
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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The University of Melbourne
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Address [1]
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Parkville
VIC 3010
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Melbourne Health's Human Research Ethics Committee
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Ethics committee address [1]
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300 Grattan Street, Parkville 3050
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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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15/10/2013
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Approval date [1]
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28/10/2013
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Ethics approval number [1]
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QA2013164
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Summary
Brief summary
This study aims to examine the impact of extra education on patients' warfarin knowledge and anticoagulation control. Who is it for? You may be eligible to join this study if you are aged 18 years or above who has been admitted to the Royal Melbourne Hospital and newly commenced on warfarin. Study details Participants in this study will be randomly allocated (by chance) to one of two groups. Participants in one group will receive the standard hospital warfarin education, delivered by pharmacists. Participants in the other group, in addition to the hospital education, will receive an extra hour of warfarin education once they have left hospital. This will be delivered by the primary investigators. All participants will be asked to complete a 20 question multiple choice test to assess their knowledge of warfarin 6 weeks after they have left hospital. We also ask participants for permission to collect their INR data to check their warfarin control. It is hoped that this project will provide guidance as to whether we need to do more to educate patients about their warfarin therapy, or whether the education system we have in place currently is sufficient.
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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
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Dr Shireen Bhatt
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Address
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Department of General Medicine
The Royal Melbourne Hospital
300 Grattan Street
VIC 3050
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Country
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Australia
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Phone
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+61429854359
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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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Shireen Bhatt
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Address
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Department of General Medicine
The Royal Melbourne Hospital
300 Grattan Street
VIC 3050
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Country
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Australia
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Phone
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+61429854359
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Fax
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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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Claire McCurdy
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Address
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Department of General Medicine
The Royal Melbourne Hospital
300 Grattan Street
VIC 3050
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Country
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Australia
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Phone
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+61418322181
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Fax
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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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