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Trial registered on ANZCTR
Registration number
ACTRN12615000241538
Ethics application status
Approved
Date submitted
9/03/2015
Date registered
17/03/2015
Date last updated
3/03/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Writing for Health: A randomised controlled trial of an online benefit-finding writing intervention for adults with type 1 or type 2 diabetes
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Scientific title
The efficacy of an online benefit-finding writing intervention versus an online use-of-time writing intervention in reducing diabetes distress in adults with type 1 or type 2 diabetes mellitus
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Secondary ID [1]
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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:
Type 1 and Type 2 diabetes mellitus
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Diabetes distress
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Diabetes self-care
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Depression
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Anxiety
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Condition category
Condition code
Mental Health
294745
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0
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Other mental health disorders
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Public Health
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0
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Other public health
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Metabolic and Endocrine
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will be randomly assigned to one of two web-based interventions on the Writing for Health online program:
Arm 1) Benefit-finding writing: Participants are asked to write online about any positive thoughts and feelings about their experience with diabetes.
Arm 2) Use of time writing (active control condition): Participants are asked to write in detail about how their time was spent that day and plans for how their time will be spent the following day and week.
Both interventions involve participants writing online, on the Internet-based Writing for Health program, for 15 minutes once a day, for three consecutive days.
Participants are asked to rate their current mood online immediately before and after each online writing session.
Participants will be sent automated emails reminding them to log on when they are due to complete a writing session or an online follow-up questionnaire.
The Writing for Health program involves an online information and consent procedure, online screening questionnaires with automatic feedback and online registration for eligible participants who provide informed consent to participate.
Participants will complete online questionnaires at pre-program, during the program, post-program and at one-month and three-month follow-up.
Participants in both arms are provided with feedback on their score categories (eg ‘mild’) on measures of symptoms of depression and anxiety, at baseline, one-month and three-month follow-up.
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Intervention code [1]
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Treatment: Other
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Intervention code [2]
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Behaviour
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Comparator / control treatment
The comparator intervention is the active control condition of writing online about use of time. Participants are asked to write in detail about how their time was spent that day and plans for how their time will be spent the following day and week.
Both the intervention group and the active control group are asked to write online for 15 minutes per day, once a day, for three consecutive days.
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Control group
Active
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Outcomes
Primary outcome [1]
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Diabetes distress as measured by the Diabetes Distress Scale. The Diabetes Distress Scale is a 17-item self-report measure of psychosocial stress associated with diabetes and includes four reliable subscales: emotional burden, physician-related distress, regime-related distress and interpersonal distress.
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Assessment method [1]
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Timepoint [1]
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Baseline, 1 month and 3 month follow-up.
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Primary outcome [2]
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Benefit finding in diabetes, as measured by the Benefit Finding Scale-Diabetes. The 17-item Benefit Finding Scale was developed to assess benefit finding in women with breast cancer, and has previously been adapted for use in diabetes.
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Assessment method [2]
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Timepoint [2]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [1]
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Diabetes self-care as measured by the Summary of Diabetes Self-Care measure.
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Assessment method [1]
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Timepoint [1]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [2]
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Anxiety symptoms, measured by the GAD-7
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Assessment method [2]
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Timepoint [2]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [3]
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Depression symptoms, measured by the PHQ-9
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Assessment method [3]
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Timepoint [3]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [4]
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Health-care utilisation, assessed by asking participants to report the number of times they have visited a doctor or other healthcare professional over the past month.
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Assessment method [4]
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Timepoint [4]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [5]
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Self-rated health, assessed by the single item ‘In general, how would you rate your health at present’, with responses rated on a five-point scale.
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Assessment method [5]
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Timepoint [5]
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Baseline, 1 month and 3 month follow-up.
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Secondary outcome [6]
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Positive and negative affect, as measured by the 10-item International Positive and Negative Affect Schedule Short Form (I-PANAS-SF) – Immediate Version
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Assessment method [6]
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Timepoint [6]
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Immediately before and after each of the three writing sessions (within intervention)
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Secondary outcome [7]
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Intervention satisfaction, as measured by the Feedback Questionnaire, which was developed specifically for this study.
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Assessment method [7]
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Timepoint [7]
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Post intervention
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Eligibility
Key inclusion criteria
Participants must be aged 18 years or older, have ever received a diagnosis of type 1 or type 2 diabetes, live in Australia, have access to the Internet, provide informed consent and be able to register online using an email address.
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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
Have received a diagnosis of a psychotic or bipolar disorder or dementia; current significant symptoms of depression (scoring 10 or above on the PHQ-9) or anxiety (scoring 8 or above on the GAD-7); current suicidal ideation; history of self-harm or suicide attempt; current psychological therapy; difficulty reading or writing in English; inability to type for 15 minutes
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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)
Interested potential participants are invited on the Writing for Health website to read the Participant Information and to provide informed consent online in order to proceed.
Potential participants are then asked to complete online screening questionnaires, which provide automatic feedback as to whether they are eligible to participate.
Eligible participants can then register online and create an account with the Writing for Health program. This process includes an automatic email being sent to the participant requesting activation of their account and a further automatic email confirming when registration is complete.
Following registration, the participant is then asked to complete further online pre-intervention questionnaires. Once completed, the participant is then informed of the condition to which they have been randomly allocated when they commence their intervention (the first writing session). The Writing for Health program software, developed using the University of New South Wales eHealth Authoring Tool, randomly allocates participants using a block design method.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated block design method
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Masking / blinding
Open (masking not 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
Repeated measures ANOVA/mixed modelling.
Data will be analysed on an intention-to-treat basis.
Previous research has reported effect sizes ranging from small to large. Assuming a medium effect size (i.e. GPower f(v) test = 0.40), power at 80%, significance set at 5% (p=.05), a sample of 73 will be required to demonstrate statistical significance. However, allowing for a 30% attrition rate, we will recruit 104 participants.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
23/03/2015
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Actual
26/03/2015
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Date of last participant enrolment
Anticipated
1/07/2016
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Actual
8/11/2016
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Date of last data collection
Anticipated
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Actual
10/02/2017
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Sample size
Target
104
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Accrual to date
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Final
88
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Faces in the Street: Urban Mental Health Research Institute, St Vincent’s Hospital, Sydney
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Address [1]
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Level 6 O’Brien Centre, St Vincent’s Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010 AUSTRALIA
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Country [1]
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Australia
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Funding source category [2]
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University
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Name [2]
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School of Psychiatry, University of New South Wales
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Address [2]
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Black Dog Institute building, Hospital Rd, Prince of Wales Hospital, Randwick, Sydney, NSW 2031, AUSTRALIA
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Country [2]
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Australia
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Primary sponsor type
Hospital
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Name
Faces in the Street: Urban Mental Health Research Institute, St Vincent’s Hospital
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Address
Level 6 O’Brien Centre, St Vincent’s Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010, AUSTRALIA
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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]
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Other collaborator category [1]
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University
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Name [1]
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School of Psychiatry, University of New South Wales
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Address [1]
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Black Dog Institute building, Hospital Rd, Prince of Wales Hospital, Randwick, Sydney, NSW, 2031, AUSTRALIA
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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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St Vincent’s Hospital Human Research Ethics Committee (HREC)
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Ethics committee address [1]
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Research Office, Level 6 deLacy Building, St Vincent’s Hospital, 390 Victoria St, Darlinghurst, NSW, 2010 AUSTRALIA
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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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19/02/2014
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Ethics approval number [1]
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HREC/13/SVH/379
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Summary
Brief summary
A randomised controlled trial will be conducted, using the online Writing for Health program, to examine the efficacy of Internet-based writing exercises focusing on benefit-finding in diabetes, versus an active control condition, in reducing diabetes distress and increasing perceived benefits of living with diabetes (primary outcomes) and reducing symptoms of depression and anxiety and increasing diabetes self-care and self-reported general health (secondary outomes). Adults with type 1 or type 2 diabetes visiting the Writing for Health website, in response to advertisements, will be invited to participate in the study. Following informed consent and an online screening procedure, participants will be randomly allocated to one of two interventions: i) Benefit-finding: Writing about any positive thoughts of feelings about experiences with diabetes; or ii) Use of time: Writing about how time has been spent this day and will be spent next week. Both interventions in the Writing for Health program involve writing online for 15 minutes once a day, for three consecutive days. Participants will complete online questionnaires at pre-intervention, during the program, post-intervention, and at one and three month follow-ups.
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Trial website
https://writingforhealth.ehat.com.au
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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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Prof Kay Wilhelm
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Address
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Faces in the Street: Urban Mental Health Research Institute and Consultation Liaison Psychiatry, St Vincent's Hospital
Level 4, O'Brien Centre, St Vincent's Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010
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Country
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Australia
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Phone
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+61 2 8382 1540
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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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Joanna Crawford
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Address
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Faces in the Street: Urban Mental Health Research Institute St Vincent's Hospital
Level 6, O'Brien Centre, St Vincent's Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010
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Country
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Australia
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Phone
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+61 2 8382 1660
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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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Joanna Crawford
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Address
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Faces in the Street: Urban Mental Health Research Institute St Vincent's Hospital
Level 6, O'Brien Centre, St Vincent's Hospital, 390 Victoria St, Darlinghurst, Sydney, NSW 2010
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Country
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Australia
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Phone
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+61 2 8382 1660
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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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