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Trial registered on ANZCTR
Registration number
ACTRN12614000705684
Ethics application status
Approved
Date submitted
17/06/2014
Date registered
3/07/2014
Date last updated
2/11/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Is the culturally adapted 9-item Patient Health Questionnaire (aPHQ-9) suitable for use as a screening tool to identify depression in Aboriginal and Torres Strait Islander people attending primary care?
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Scientific title
Is the culturally adapted 9-item Patient Health Questionnaire (aPHQ-9) suitable for use as a screening tool to identify depression in Aboriginal and Torres Strait Islander people attending primary care?
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Secondary ID [1]
284767
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Nil
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Universal Trial Number (UTN)
Nil
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Trial acronym
Getting it right: the validation study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Depression
292139
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Condition category
Condition code
Mental Health
292474
292474
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0
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Depression
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Public Health
292639
292639
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0
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Health service research
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Five Aboriginal language groups of Central Australian Aboriginal men independently selected the 9-item Patient Health Questionnaire (PHQ-9) depression screening tool from a selection of depression screening tools, as the most appropriate to adapt for use with Indigenous people. The PHQ-9 was adapted to the local needs of all five language groups over 12-months and consensus regarding wording was reached. The PHQ-9 wording was modified, using simplified English, to make the ‘adapted PHQ-9’ (aPHQ-9) culturally meaningful and give it face validity. In qualitative interviews with the same participants, seven critical domains of depressive experience within Indigenous men were identified that were not covered in existing depression case-finding measures: anger, weakened spirit, homesickness, irritability, excessive worry, rumination, and drug/alcohol use.
Following consent participants will complete two separate interviews up to one week apart.
Interview 1: the adapted PHQ-9 and additional 7 questions will be administered (face to face) by a trained member of the primary health care service’s staff followed by demographic questions. (Up to 20 minutes)
Interview 2: MINI International Neuropsychiatric Interview 6.0.0. will be administered (face to face) by a trained member of the primary health care service’s staff or by a centralised interviewer (over the telephone) (Up to 20 minutes)
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Intervention code [1]
289562
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Not applicable
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Comparator / control treatment
Not applicable
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The clinicial diagnosis of depression according to the MINI 6.0.0, having two categories: "major depressive episode" and "no major depressive episode".
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Assessment method [1]
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Timepoint [1]
292340
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Baseline
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Secondary outcome [1]
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Participant's acceptability of different aspects of the aPHQ-9.
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Assessment method [1]
308733
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Timepoint [1]
308733
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This will be measured in 5-points Likert scales within one week of aPHQ-9 interview.
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Secondary outcome [2]
309038
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Feasibility of assessment within PHCS services. Should the aPHQ-9 (with or without the addition of one or more of the seven additional questions) have acceptable sensitivity and specificity as a screening tool for depression we will seek qualitative feedback on feasibility from PHCS staff during the feedback of study results to sites.
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Assessment method [2]
309038
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Timepoint [2]
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Semi-structured interviews will be used to assess this outcome. Site staff will be asked about the burden screening placed on them, their participants and the practice, the effect on the participant/clinician relationship, the usefulness of the aPHQ-9 and the extent to which practice routines must be adapted to integrate the aPHQ-9 into their service delivery.
This will be completed within 6 months of finishing study recruitment.
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Eligibility
Key inclusion criteria
Aged 18 years
Self identifies as Aboriginal or Torres Strait Islander
Attending a primary health care service in Australia
Able to communicate sufficiently to complete study instruments
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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
Known psychosis
Known bipolar disorder
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Study design
Purpose
Psychosocial
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
We computed the sample size based on the target precision for the estimation of sensitivity and specificity of the aPHQ-9 used for the screening of a major depressive episode (MDE). Assuming a MDE prevalence (assessed by the MINI 6.0.0) of 10% and a true sensitivity of 0.85, a sample size of 500 participants will give us a precision of 0.1 for the sensitivity’s 95% confidence interval. For the specificity, 500 participants will provide a precision of 0.04 for the specificity’s 95% confidence interval, assuming a true specificity of 0.75 and the same prevalence of 10%. If the prevalence of MDE is in fact higher, for example 15%, the precision for the sensitivity will be 0.08.
For the analysis of the contribution of additional questions to the aPHQ-9, a sample size of 500 will give us 80% probability (power) of detecting a true improvement of 0.05 in the area under the ROC curve, fixing the type I error at 0.05.
For descriptive purposes baseline characteristics will be presented. Discrete variables will be summarised by frequencies and percentages, continuous variables by use of standard measures of central tendency and dispersion, mean and standard deviation (SD) or median and interquartile range (IQR).
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/10/2014
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Actual
25/03/2015
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Date of last participant enrolment
Anticipated
1/09/2016
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Actual
4/11/2016
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Date of last data collection
Anticipated
23/12/2016
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Actual
16/11/2016
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Sample size
Target
500
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Accrual to date
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Final
500
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,WA
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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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National Health and Medical Research Council (NHMRC), Australia
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Address [1]
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National Health and Medical Research Council
GPO Box 1421
Canberra ACT 2601
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Country [1]
289384
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Australia
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Primary sponsor type
Individual
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Name
A/Prof Maree Hackett
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Address
The George Institute
PO Box M201 Missenden Rd
Camperdown, NSW 2050
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Country
Australia
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Secondary sponsor category [1]
288071
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None
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Name [1]
288071
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Address [1]
288071
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Country [1]
288071
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291148
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The University of Sydney Human Research Ethics Committee
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Ethics committee address [1]
291148
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Level 6, Jane Foss Russell The University of Sydney NSW 2006
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Ethics committee country [1]
291148
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Australia
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Date submitted for ethics approval [1]
291148
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21/04/2014
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Approval date [1]
291148
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19/05/2014
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Ethics approval number [1]
291148
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2014/361
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Ethics committee name [2]
292837
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Aboriginal Health and Medical Research Council in NSW
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Ethics committee address [2]
292837
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PO Box 1565 STRAWBERRY HILLS NSW 2012
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Ethics committee country [2]
292837
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Australia
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Date submitted for ethics approval [2]
292837
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Approval date [2]
292837
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28/01/2015
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Ethics approval number [2]
292837
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EC00342
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Ethics committee name [3]
292838
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ACT Health Human Research Ethics Committee
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Ethics committee address [3]
292838
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Building 10 level 6 Canberra Hospital PO Box 11 WODEN ACT 2606
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Ethics committee country [3]
292838
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Australia
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Date submitted for ethics approval [3]
292838
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Approval date [3]
292838
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22/09/2014
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Ethics approval number [3]
292838
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EC00100
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Ethics committee name [4]
292839
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Metro South Human Research Ethics Committee
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Ethics committee address [4]
292839
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Princess Alexandra Hospital Level 7 Translational Research Institute 37 Kent Street WOOLLOONGABBA QLD 4102
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Ethics committee country [4]
292839
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Australia
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Date submitted for ethics approval [4]
292839
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Approval date [4]
292839
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16/10/2014
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Ethics approval number [4]
292839
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EC00167
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Ethics committee name [5]
292840
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Central Australian Human Research Ethics Committee
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Ethics committee address [5]
292840
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Central Australian Human Research Ethics Committee PO Box 4066 ALICE SPRINGS NT 0871
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Ethics committee country [5]
292840
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Australia
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Date submitted for ethics approval [5]
292840
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Approval date [5]
292840
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18/03/2015
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Ethics approval number [5]
292840
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EC00155
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Ethics committee name [6]
292841
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Human Research Ethics Committee for the Northern Territory Department of Health and Menzies School of Health Research
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Ethics committee address [6]
292841
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PO Box 41096 CASUARINA NT 0810
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Ethics committee country [6]
292841
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Australia
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Date submitted for ethics approval [6]
292841
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Approval date [6]
292841
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23/02/2015
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Ethics approval number [6]
292841
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EC00153
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Ethics committee name [7]
293771
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Aboriginal Health Council of South Australia - Aboriginal Health Research Ethics Committee
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Ethics committee address [7]
293771
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PO Box 981 UNLEY, SA 5061
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Ethics committee country [7]
293771
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Australia
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Date submitted for ethics approval [7]
293771
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07/07/2015
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Approval date [7]
293771
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07/07/2015
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Ethics approval number [7]
293771
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04-15-622
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Ethics committee name [8]
294044
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Western Australian Aboriginal Health Ethics Committee
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Ethics committee address [8]
294044
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450 Beaufort St, Highgate WA 6003
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Ethics committee country [8]
294044
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Australia
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Date submitted for ethics approval [8]
294044
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01/10/2015
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Approval date [8]
294044
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24/11/2015
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Ethics approval number [8]
294044
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670
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Summary
Brief summary
This cross sectional project will involve 500 Indigenous primary care attendees in Australia’s States and Territories. We will validate (criterion validity) the aPHQ-9 as a screening tool, alone, and in combination with the additional seven questions, against a gold standard structured criterion interview for depression The Mini International Neuropsychiatric Interview (MINI ) 6.0.0 (criterion standard), in Indigenous men and women attending primary health care services across Australia. This will provide the evidence on whether to recommend use of the aPHQ-9 as a screening tool for depression in health services research, clinical care delivery and policy evaluation in Federal and State chronic diseases programmes.
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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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A/Prof Maree Hackett
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Address
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The George Institute
PO BOX M201 Missenden Rd
Camperdown NSW 2050
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Country
49098
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Australia
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Phone
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+61 2 8052 4502
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Fax
49098
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+61 2 9993 4502
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Email
49098
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[email protected]
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Contact person for public queries
Name
49099
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Sara Farnbach
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Address
49099
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The George Institute
PO BOX M201 Missenden Rd
Camperdown NSW 2050
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Country
49099
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Australia
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Phone
49099
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+61 2 9993 4571
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Fax
49099
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+61 2 8052 4571
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Email
49099
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[email protected]
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Contact person for scientific queries
Name
49100
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Maree Hackett
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Address
49100
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The George Institute
PO BOX M201 Missenden Rd
Camperdown NSW 2050
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Country
49100
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Australia
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Phone
49100
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+61 2 8052 4502
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Fax
49100
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+61 2 9993 4502
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Email
49100
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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
Getting it Right: Study protocol to determine the diagnostic accuracy of a culturally-specific measure to screen for depression in Aboriginal and/or Torres Strait Islander people.
2016
https://dx.doi.org/10.1136/bmjopen-2016-015009
N.B. These documents automatically identified may not have been verified by the study sponsor.
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