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Trial registered on ANZCTR
Registration number
ACTRN12617000957392
Ethics application status
Approved
Date submitted
22/06/2017
Date registered
4/07/2017
Date last updated
4/07/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
LEAD - Lung cancer diagnostic and treatment pathways: a comparison between Culturally and Linguistically Diverse (CALD) and Anglo-Australian patients
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Scientific title
LEAD - Lung cancer diagnostic and treatment pathways: a comparison between Culturally and Linguistically Diverse (CALD) and Anglo-Australian patients
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Secondary ID [1]
292256
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1100024
This is the ID number allocated by the funding organisation (i.e. Cancer Council Australia)
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Universal Trial Number (UTN)
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Trial acronym
LEAD
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
lung cancer
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Condition category
Condition code
Public Health
303138
303138
0
0
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Health service research
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Cancer
303139
303139
0
0
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Lung - Non small cell
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Cancer
303140
303140
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0
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Lung - Small cell
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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
The LEAD project has a mixed-method, observational cohort design. The quantitative arm comprises a patient survey, a review of general practice records, and a case-note analysis of hospital records to collect data relevant to the four time intervals. The qualitative arm comprises interviews with lung cancer patients, general practitioners (GPs) and hospital specialists. Data will be collected once only at the time of data collection and the period of observation in each participant will be from the patient noticing symptoms to the commencement of first treatment
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Intervention code [1]
298422
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Not applicable
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Comparator / control treatment
The study will compare the differences between CALD and Anglo-Australian patients in the four time intervals along the lung cancer diagnostic and pre-treatment pathway.
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Control group
Active
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Outcomes
Primary outcome [1]
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The first primary outcome variable is the length of the appraisal interval along the cancer diagnostic and pre-treatment pathway. The definition and measurement of this interval are guided by the Models of Pathway to Treatment (Walter et al., 2012). This time interval will be estimated using the Kaplan-Meier method and will be compared between the two patient groups using a log-rank test. Data will be collected through the patient survey.
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Assessment method [1]
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Timepoint [1]
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Once only at the time of data collection.
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Primary outcome [2]
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The second primary outcome variable is the length of the help-seeking interval along the cancer diagnostic and pre-treatment pathway. The definition and measurement of this interval are guided by the Models of Pathway to Treatment (Walter et al., 2012). This time interval will be estimated using the Kaplan-Meier method and will be compared between the two patient groups using a log-rank test. Data will be collected through the patient survey and the GP review.
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Assessment method [2]
302563
0
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Timepoint [2]
302563
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Once only at the time of data collection.
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Primary outcome [3]
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The third outcome variable is the length of the diagnostic and the pre-treatment intervals along the cancer diagnostic and pre-treatment pathway. The definition and measurement of these intervals are guided by the Models of Pathway to Treatment (Walter et al., 2012). These time intervals will be estimated using the Kaplan-Meier method and will be compared between the two patient groups using a log-rank test. Data will be collected through the GP review and the case-note analysis of hospital medical records.
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Assessment method [3]
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Timepoint [3]
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Once only at the time of data collection.
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Secondary outcome [1]
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The first group of secondary outcome is patients' cancer and demographic variables. These include type and staging of cancer, patients' attitudes and beliefs, English proficiency, education levels, etc. Data will be collected through the patient survey, the case-note analysis, and the patient interview.
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Assessment method [1]
336278
0
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Timepoint [1]
336278
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Once only at the time of data collection.
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Secondary outcome [2]
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The second group of secondary outcome is heath care provider related variables. These include GP demographics and billing practices, types of specialists seen, etc. Data will be collected through the GP review, the case-note analysis and interviews with GPs and specialists.
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Assessment method [2]
336374
0
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Timepoint [2]
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Once only at the time of data collection.
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Secondary outcome [3]
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The third group of secondary outcome is health system related variables . These include involvement of a multidisciplinary team, types and places of investigations undertaken, etc.Data will be collected through the case-note analysis and interviews with GPs and specialists.
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Assessment method [3]
336375
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Timepoint [3]
336375
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Once only at the time of data collection.
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Eligibility
Key inclusion criteria
The patients need to meet two inclusion criterion: (1) be diagnosed with primary lung cancer at the study sites within the past month or during the recruitment phase, and (2) be CALD or Anglo-Australian patients. CALD patients are those who speak one of the following five languages at home or listing these languages as their preferred language: Greek, Italian, Vietnamese, Arabic and Chinese (including Cantonese and Mandarin). Anglo-Australian patients are those (1) being born in Australia or other major English-speaking countries (Canada, New Zealand, the United Kingdom, and the US), and (2) listing English as their preferred language.
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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
Patients who are pregnant or aged under 18 years will be excluded.
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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
Both
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Statistical methods / analysis
Quantitative arm: Data from the patient survey, the GP review and the case-note analysis will be entered into separate databases. For patients who return the survey and provide consent for access to their hospital and general practice medical records, a unique participant ID will be created, which will be used to link data from the three databases. For those who do not provide consent, no data linkage will be performed. The four time intervals will be estimated using the Kaplan-Meier method and will be compared between the two patient groups using a log-rank test. The Cox proportional hazards model will be performed to examine any associations between the time intervals and patient, healthcare provider, and health systems factors. Chi-square tests will be used to compare categorical variables between the two groups. Exploratory analyses may be performed by adjusting for patients’ characteristics using logistic regression. These analyses will be conducted using SPSS 24.
Quantitative arm: All interviews will be audio-taped, and transcription, translation, coding, and analysis will occur concurrently with data collection. Thematic analysis will be conducted using a constant comparative method to identify similarities and differences in the content (Ryan & Bernard, 2003). Data will be analysed inductively and deductively. The interviews will then be incorporated into NVivo ver.10 for more structured coding and analysis.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
15/05/2017
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Date of last participant enrolment
Anticipated
31/12/2018
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Actual
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Date of last data collection
Anticipated
29/03/2019
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Actual
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Sample size
Target
1064
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
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Recruitment hospital [1]
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The Alfred - Prahran
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Recruitment hospital [2]
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [3]
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Royal Melbourne Hospital - City campus - Parkville
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Recruitment hospital [4]
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Sunshine Hospital - St Albans
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Recruitment hospital [5]
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Peter MacCallum Cancer Centre - Melbourne
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Recruitment hospital [6]
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Box Hill Hospital - Box Hill
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Recruitment hospital [7]
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [8]
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The Northern Hospital - Epping
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Recruitment hospital [9]
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Royal Prince Alfred Hospital - Camperdown
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Recruitment hospital [10]
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Princess Alexandra Hospital - Woolloongabba
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Recruitment postcode(s) [1]
16487
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3004 - Prahran
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Recruitment postcode(s) [2]
16488
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3168 - Clayton
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Recruitment postcode(s) [3]
16489
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3050 - Parkville
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Recruitment postcode(s) [4]
16490
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3021 - St Albans
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Recruitment postcode(s) [5]
16491
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3000 - Melbourne
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Recruitment postcode(s) [6]
16492
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3128 - Box Hill
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Recruitment postcode(s) [7]
16493
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3084 - Heidelberg
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Recruitment postcode(s) [8]
16494
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3076 - Epping
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Recruitment postcode(s) [9]
16495
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2050 - Camperdown
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Recruitment postcode(s) [10]
16496
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4102 - Woolloongabba
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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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Cancer Council Australia
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Address [1]
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GPO Box 4708, Sydney NSW 2001
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Country [1]
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Australia
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Funding source category [2]
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Government body
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Name [2]
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Cancer Australia
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Address [2]
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Locked Bag 3, STRAWBERRY HILLS NSW 2012
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Country [2]
296834
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Australia
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Primary sponsor type
University
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Name
Monash University
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Address
Monash University, Victoria 3800, 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]
295790
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Address [1]
295790
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Country [1]
295790
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
298037
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Monash Health HREC
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Ethics committee address [1]
298037
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Research Support Services Level 2, i Block, Monash Medical Centre 246 Clayton Road CLAYTON VIC 3168
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Ethics committee country [1]
298037
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Australia
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Date submitted for ethics approval [1]
298037
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21/09/2016
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Approval date [1]
298037
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26/10/2016
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Ethics approval number [1]
298037
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HREC/16/MonH/311
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Summary
Brief summary
This study aims to compare the diagnostic and treatment pathways between Culturally and Linguistically Diverse (CALD) and Anglo-Australian lung cancer patients. Who is it for? You may be eligible to join this study if you are aged 18 years or above and be diagnosed with primary lung cancer at the study sites within the past month or during the recruitment phase. Study details You will be asked to complete a patient survey and/or have a face-to-face interview with the researcher. We will also ask whether we can access your hospital medical records and contact your GP for medical information related to your cancer diagnosis. Study significance This study will provide important information about the barriers existing along the lung cancer pathway from symptom appraisal to treatment in CALD populations and is essential to any future intervention to improve early diagnosis and treatment for lung cancer.
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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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Prof Danielle Mazza
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Address
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Department of General Practice
School of Primary and Allied Health Care
Faculty of Medicine, Nursing and Health Sciences
Monash University
Building 1, 270 Ferntree Gully Road
Notting Hill, Vic 3168
Australia
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Country
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Australia
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Phone
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+61 3 9902 4512
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Fax
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+61 3 9902 4300
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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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Xiaoping Lin
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Address
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Department of General Practice
School of Primary and Allied Health Care
Faculty of Medicine, Nursing and Health Sciences
Monash University
Building 1, 270 Ferntree Gully Road
Notting Hill, Vic 3168
Australia
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Country
75779
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Australia
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Phone
75779
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+61 3 9902 4481
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Fax
75779
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+61 3 9902 4300
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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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Xiaoping Lin
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Address
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Department of General Practice
School of Primary and Allied Health Care
Faculty of Medicine, Nursing and Health Sciences
Monash University
Building 1, 270 Ferntree Gully Road
Notting Hill, Vic 3168
Australia
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Country
75780
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Australia
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Phone
75780
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+61 3 9902 4481
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Fax
75780
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+61 3 9902 4300
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Email
75780
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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
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Plain language summary
No
The main outcome paper has been submitted to a pee...
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Documents added automatically
No additional documents have been identified.
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