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Trial registered on ANZCTR
Registration number
ACTRN12609000497202
Ethics application status
Approved
Date submitted
17/06/2009
Date registered
22/06/2009
Date last updated
6/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Help-seeking for Depression by Young People - considering the impact of Stigma
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Scientific title
A randomised control trial for the effectiveness of a mental health literacy intervention promoting a biological model of depression to facilitate a reduction in stigma and increase help-seeking intention in young people
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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:
The effectiveness of a mental health literacy intervention promoting a biological model of depression to facilitate a reduction in stigma and increase help-seeking intention in young people
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Condition category
Condition code
Mental Health
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Depression
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Public Health
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0
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Epidemiology
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Public Health
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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
It will comprise a randomised control trial (RCT) where students are randomly assigned to one of three educational paradigms: a biological attribution condition, a psychosocial attribution condition or a control condition involving the provision of general information about depression. The intervention will be delivered online.
The Biological Condition
Content for this experimental intervention will include a vignette outlining information about the biological basis for depression. The general message will be that 'Depression is an illness like any other illness' and that the onset of depression is due to a chemical imbalance in the brain.
The Psychosocial Condition
Content for this experimental intervention will include a vignette outlining information about the psychosocial basis for depression. The general message will be that depression results from the stress in our social environment and our reactions to it.
The survey and intervention will be completed online in one lesson of the normal class schedule (approximately 50 minutes), in a one-off educational intervention.
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Intervention code [1]
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Behaviour
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Comparator / control treatment
This intervention will comprise a vignette and standard general information around depression which focuses on the symptoms experienced by a person with depression (eg. trouble sleeping, low mood, irritability, feeling lethargic) without providing a causal explanation.
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Control group
Active
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Outcomes
Primary outcome [1]
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Reduction in anticipated self-stigma for depression
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Assessment method [1]
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Timepoint [1]
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Immediately post-intervention using Barney's (2007) Self-Stigma for Depression Scale (SSDS)
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Secondary outcome [1]
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Increased general help-seeking intention by young people for depression
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Assessment method [1]
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Timepoint [1]
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Immediately post-intervention using Rickwood's General Help-Seeking Questionnaire (GHSQ)
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Eligibility
Key inclusion criteria
This will be a universal intervention (ie, participants selected regardless of mental health status) involving all Year 11 and 12 students in each college.
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Minimum age
16
Years
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Maximum age
20
Years
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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
15 years or under.
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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)
We anticipate that all Year 11 and 12 students in the consenting colleges will be invited to participate. We propose operating on the basis of passive consent for participation from the parents/guardians of students and informed consent (via online acceptance) from each student who participates.
The participants will be young mature minors aged 16 to 18 years. As college students they are likely to have achieved a sufficient maturity and competence to enable them to understand fully what is proposed (NS4.2a: Consent by children under the age of majority but with sufficient competence to decide).
We anticipate that the young person's consent is implied by clicking on the “I agree” button at the bottom of the online Information and Consent page and by completing the questionnaire and intervention. .
Parental consent is normally required where an anonymous questionnaire is to be administered to children in schools. However, the experience of other researchers in schools is that there are major barriers to receiving back such permission forms in the school context as they become lost in bags or otherwise mislaid or overlooked. Given the age and educational level of the students, potential benefits of the study and the low level of risk (particularly as the survey is anonymous and no data can be linked to individual students) and the provision of opt-out options for parents, we ask that the committee approve the proposed implied consent from parents and active consent from young people.
Conditions are randomly allocated to students via a sealed white envelope, inside which is a piece of paper with a 'password' code that is required to be entered into the online environment. Each group has a unique colour code allocated to that condition.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Participants will be randomly allocated to one of three intervention conditions. The randomisation will occur via sealed intervention envelopes, prepared by a statistician who will prepare the intervention envelopes using a computer based random number generator, independently of the primary investigator prior to the intervention taking place.
Envelopes are then handed out in order to the school students as they sit at the computers.
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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
This intervention will be delivered in a single lesson over approximately 50 minutes. Each participant will complete an online survey with data collected on a server hosted behind a firewall by the Centre for Mental Health Research. The first screen will ask for the participants consent and when consent is provided then each participant will independently work through the online questionnaire. Participants will be randomly allocated into a group via the manual process outlined earlier. Data extraction will be automated and no identifying information will be collected from participants or attached to data.
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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
Not yet recruiting
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Date of first participant enrolment
Anticipated
19/06/2009
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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
480
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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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University
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Name [1]
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Australian National University
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Address [1]
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Centre for Mental Health Research
College of Medicine, Biology and Environment
Eggleston Road
Acton ACT 0200
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Australian National University
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Address
School of Psychology
Building 39
Australian National University
Acton ACT 0200
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Kerry Howard
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Address [1]
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PO Box 4003
WESTON CREEK ACT 2611
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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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Australian National University Human Research Ethics Committee
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Ethics committee address [1]
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Research Office Chancelry Building 10B LG East Road Australian National University Acton ACT 0200
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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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11/05/2009
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Approval date [1]
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03/06/2009
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Ethics approval number [1]
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2009/208
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Summary
Brief summary
Based on biological attribution theory it is hypothesised that the biological explanation for depression will lead to a greater decrease in young peoples’ anticipated self-stigma associated with depression than the other two conditions. It is further hypothesised that any decrease in self-stigma will lead to increased help-seeking intention (from a mental health professional) by these young people if they were to experience depression in the future.
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Trial website
https://mentalhealth.anu.edu.au/survey
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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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Kerry Howard
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Address
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PO Box 4003
WESTON CREEK ACT 2611
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Country
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Australia
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Phone
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+61 2 6287 1019
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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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Professor Kathy Griffiths
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Address
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Centre for Mental Health Research
Australian National University
Eggleston Road
ACTON ACT 2601
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Country
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Australia
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Phone
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+61 2 6125 9723
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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
Source
Title
Year of Publication
DOI
Embase
Can a brief biologically-based psychoeducational intervention reduce stigma and increase help-seeking intentions for depression in young people? A randomised controlled trial.
2018
https://dx.doi.org/10.2989/17280583.2018.1467323
N.B. These documents automatically identified may not have been verified by the study sponsor.
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