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Trial registered on ANZCTR
Registration number
ACTRN12611000254998
Ethics application status
Approved
Date submitted
11/02/2011
Date registered
8/03/2011
Date last updated
15/12/2011
Type of registration
Prospectively registered
Titles & IDs
Public title
Social Desirability Bias in response to a health behaviour survey
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Scientific title
Experimental study of the effects of introducing social desirability bias in responses to a health behaviour survey.
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Secondary ID [1]
253395
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Nil
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Universal Trial Number (UTN)
U1111-1119-0270
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Trial acronym
SDB
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Social desirability bias in health survey responses
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Condition category
Condition code
Public Health
259087
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0
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Other public health
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Behavioural: All participants will be asked to complete a short (5 minute) web-based survey. The initial part of the survey will be comprised of questions about physical activity, diet, smoking and alcohol intake. All participants will answer the same questions for each section apart from alcohol where participants will be randomised to one of two groups (A or B). The Group A survey will be titled “Recent Drinking” and followed by 3 questions regarding alcohol intake over the past 4 weeks. The Group B survey will be titled “Alcohol Use Disorders” and a brief introduction will say the questions are used to identify alcohol use disorders followed by 7 behavioural questions. They will then see a heading of “Recent Drinking” followed by the same 3 questions from Group A concerning alcohol intake over the past 4 weeks. The entire web-based survey will have a median completion time of less than 5 minutes.
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Intervention code [1]
257841
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Behaviour
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Comparator / control treatment
Comparision of 2 survey types.
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Control group
Active
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Outcomes
Primary outcome [1]
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Self-reported volume of alcohol in the previous 4 weeks.
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Assessment method [1]
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Timepoint [1]
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At the time of the survey
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Primary outcome [2]
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Self-reported frequency of drinking in the previous 4 weeks.
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Assessment method [2]
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Timepoint [2]
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A the time of the survey.
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Primary outcome [3]
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Self-reported amount consumed per typical drinking occassion in the previous 4 weeks.
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Assessment method [3]
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Timepoint [3]
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At the time of the survey.
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Secondary outcome [1]
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Nil
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Assessment method [1]
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Timepoint [1]
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Nil
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Eligibility
Key inclusion criteria
English speaking adults who are 18 years and over
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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?
Yes
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Key exclusion criteria
Nil
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Study design
Purpose of the study
Treatment
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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)
Students will be invited to participate via an email sent to their student address. This email will contain a hyperlink to the study Information Sheet. Clicking on this link to complete the survey will be taken as consent. A reminder email will be sent two weeks later. All participants will be asked to complete a short web-based survey. The initial part of the survey will be comprised of questions about physical activity, diet, smoking and alcohol intake. All participants will be randomised to one of two conditions (A or B) for the alcohol questions. Randomisation will occur without their knowledge.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation will be effected by computer using a random number generator.
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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
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
17/10/2011
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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
4200
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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]
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Government body
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Name [1]
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Australian Research Council
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Address [1]
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1st Floor, 8 Brindabella Circuit, Brindabella
Business Park, CANBERRA AIRPORT ACT 2609
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
A/Prof Kypors Kypri
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Address
University of Newcastle, School of Medicine and Public Health, Level 3, David Maddison Building, Corner Watt and King Streets, Newcastle, NSW 2300
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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]
257618
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Country [1]
257618
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Human Research Ethics Committee University of Newcastle
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Ethics committee address [1]
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Human Research Ethics Administration Research Services Research Office The University of Newcastle Callaghan NSW 2308
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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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01/09/2010
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Approval date [1]
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07/02/2011
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Ethics approval number [1]
260453
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H-2010-1243
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Summary
Brief summary
This study aims to test experimental hypotheses which will assist in improving the design of behavioural intervention trials, and inform the interpretation of findings reported to date, leading to better decisions about health policy and clinical practice.
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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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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Amanda Wilson
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Address
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University of Newcastle, School of Medicine and Public Health, Level 3, David Maddison Building, Corner Watt and King Streets, Newcastle, NSW 2300
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Country
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Australia
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Phone
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+61 2 49138297
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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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A/Prof Kypros Kypri
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Address
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University of Newcastle, School of Medicine and Public Health, Level 3, David Maddison Building, Corner Watt and King Streets, Newcastle, NSW 2300
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Country
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Australia
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Phone
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+61 2 49138231
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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.
Download to PDF