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Trial registered on ANZCTR
Registration number
ACTRN12617001602314
Ethics application status
Approved
Date submitted
7/11/2017
Date registered
7/12/2017
Date last updated
7/12/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effectiveness of a new social intervention to increase community connectedness and reduce isolation in adults transitioning home after long term hospital care: The Groups 4 Health Trial
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Scientific title
Effectiveness of a new social intervention to increase community connectedness and reduce psychological distress in adults transitioning home after long term hospital care: The Groups 4 Health trial.
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Secondary ID [1]
293301
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None
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Universal Trial Number (UTN)
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Trial acronym
G4H Trial
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
depression
305384
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social anxiety
305385
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Condition category
Condition code
Mental Health
304670
304670
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0
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Depression
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Mental Health
304671
304671
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0
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Anxiety
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Groups 4 Health Trial:
G4H is a manualized program that seeks to increase social connectedness by building group-based social identifications in the context of an in-vivo group experience. The five modules give people the knowledge and skills they need to manage their social group memberships, and the identities that underpin them, effectively.
The intervention comprises 5 x 1.5 hour face-to-face group facilitated sessions, run weekly in the first month with the final module 5 delivered 1 month later. Modules 1-4 have associated homework after each session which takes about 30 minutes. The program is delivered in the Psychology Clinic of the School of Psychology, University of Queensland. Facilitators are Clinical and Health Psychology postgraduate students who receive training and weekly supervision to deliver the program.
Module content is summarised below.
Module 1: Schooling. Raises awareness of the beneficial effects that social group memberships have for health. It highlights the costs of ignoring the social dimensions of health and points out that failure to use all the social resources at our disposal generally leads to suboptimal health outcomes. The module also makes the point that it is within people’s power to counter these effects by learning how best to develop, maintain and harness group-based resources.
Module 2: Scoping. Focuses on the range of group-based resources that people have, or ideally should have at their disposal, to optimize health. This module engages participants in the process of social identity mapping (Cruwys, Steffens, Haslam, et al., 2015). This tool was developed to explore respondents’ social identities, in order to assess their current social functioning and develop a sense of how they would ideally like to function in the futureIdentifying current group memberships and any gaps in group networks.
Module 3: Sourcing. Targets development of skills needed to identify and strengthen existing valued social identities with a view to optimizing and sustaining these in the longer term. It also raises awareness of solutions to barriers to making the most of existing groups.
Module 4: Scaffolding. Uses the G4H group as a model for establishing and embedding new social group connections whilst at the same time exploring strategies to identify which connections to develop and enact through a social plan of action. The goal is to trial these social plans between this and the final module, which takes place at least one month later.
Module 5: Sustaining: Is a booster session held one month later that aims to troubleshoot any difficulties that have arisen in the course of implementing these social plans. It also revisits social identity maps, created in Module 2, to see how they have developed in the course of the program. The social foundations that have been identified and developed in the preceding four modules are also reviewed with a view to encouraging their long-term maintenance.
In addition to the facilitator manual, the program is supported by a client workbook. This contains a summarized version of the facilitator’s manual highlighting the main activities and learning points for each session, with sufficient space to complete activities (both within the sessions and as homework) and document any relevant notes and plans to achieve particular goals.
Treatment fidelity is assessed by brief questionnaire completed by facilitators at the end of each session delivered. This requires facilitators to tick off session activities covered, rate alliance and rapport between participants and with facilitator, indicate the length of session, and rate session satisfaction and ease of delivery.
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Intervention code [1]
299559
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Treatment: Other
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Comparator / control treatment
Wait-list control commenced after 4 months
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Control group
Active
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Outcomes
Primary outcome [1]
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mean Roberts UCLA Loneliness Scale score
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Assessment method [1]
303882
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Timepoint [1]
303882
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Baseline, on completion of G4H (primary endpoint), 2 months after completion of G4H
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Secondary outcome [1]
340349
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mean depression sub scale score from the Depression Anxiety and Stress Scale
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Assessment method [1]
340349
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Timepoint [1]
340349
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baseline, on completion of G4H, 2 months after completion of G4H
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Secondary outcome [2]
340350
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Average rating on multiple group membership scale (published scale comprising 4 items)
Citation: Haslam, C., Holme, A., Haslam, S.A., Iyer, A., Jetten, J., & Williams, W.H. (2008). Maintaining group membership: Identity continuity and well-being after stroke Neuropsychological Rehabilitation, 18, 671-691
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Assessment method [2]
340350
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Timepoint [2]
340350
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baseline, on completion of G4H, 2 months after completion of G4H
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Secondary outcome [3]
340604
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mean mini-SPIN
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Assessment method [3]
340604
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Timepoint [3]
340604
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baseline, at completion of G4H, 2 months after completion of G4H
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Secondary outcome [4]
340605
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Number of general practitioner appointments in last month (self report)
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Assessment method [4]
340605
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Timepoint [4]
340605
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baseline, at completion of G4H, 2 months after completion of G4H
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Eligibility
Key inclusion criteria
1. Diagnosed with mental illness by health professional or
2. Scoring above the threshold (i.e., > 5) on the Patient Health Questionnaire - 9 (PHQ-9).
3. perceived social isolation
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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
1. known neurological condition
2. known history of psychosis
3. Unstable and fluctuating mental health condition that would interfere with taking part in a group program
4. severe learning impairment
5. non-English speaking
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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)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation by computer software
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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
Other
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Other design features
Wait list control
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Power analyses were conducted based on the pre-post effect size for the primary outcome (loneliness) found in pilot data (d = 0.86; Haslam et al., 2016). This suggests a minimum of 23 participants would need to be retained in each condition at follow-up for 80% power (Lehr, 1992). Drawing on the retention data from pilot study (of 67%) aimed to recruit 65 participants in each condition at baseline
Analysis strategy:
Separate repeated measures ANOVA to assess the effect of intervention on primary and secondary outcomes, both with intention-to treat (where outcome data is estimated using carry forward of last available observations) and per protocol analyses (only including participants who met eligibility criteria, were randomly assigned, and completed the intervention according to the protocol, and had both baseline and follow-up data).
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
20/04/2015
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Date of last participant enrolment
Anticipated
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Actual
20/02/2017
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Date of last data collection
Anticipated
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Actual
12/06/2017
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Sample size
Target
130
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Accrual to date
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Final
121
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment postcode(s) [1]
18036
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4072 - University Of Queensland
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Recruitment postcode(s) [2]
18037
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4068 - Taringa
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Recruitment postcode(s) [3]
18038
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4066 - Toowong
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Recruitment postcode(s) [4]
18039
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4101 - West End
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Recruitment postcode(s) [5]
18040
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4103 - Annerley
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Recruitment postcode(s) [6]
18041
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4102 - Woolloongabba
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Recruitment postcode(s) [7]
18042
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4101 - South Brisbane
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Recruitment postcode(s) [8]
18043
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4068 - Indooroopilly
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Recruitment postcode(s) [9]
18044
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4169 - Kangaroo Point
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Recruitment postcode(s) [10]
18045
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4000 - Brisbane
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Recruitment postcode(s) [11]
18046
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4060 - Ashgrove
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Recruitment postcode(s) [12]
18047
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4064 - Paddington
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Funding & Sponsors
Funding source category [1]
297926
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University
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Name [1]
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University of Queensland
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Address [1]
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School of Psychology
University of Queensland
St Lucia, 4072, QLD
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Country [1]
297926
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Australia
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Primary sponsor type
University
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Name
University of Queensland
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Address
University of Qld, St Lucia, Qld, 4072
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Country
Australia
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Secondary sponsor category [1]
296988
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None
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Name [1]
296988
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Address [1]
296988
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Country [1]
296988
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
298972
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Behavioural and Social Sciences Ethical Research Committee
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Ethics committee address [1]
298972
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University of Qld, St Lucia, Qld, 4072
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Ethics committee country [1]
298972
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Australia
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Date submitted for ethics approval [1]
298972
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12/01/2015
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Approval date [1]
298972
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05/03/2015
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Ethics approval number [1]
298972
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2014000731
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Summary
Brief summary
Social isolation is a major health risk and for many is associated with psychological distress. A new social group intervention, Groups 4 Health (G4H), has strong potential to address this problem. G4H is a five-module, manualized program that seeks to increase social connectedness by building group-based social identifications in the context of an in-vivo group experience. Its effectiveness has already demonstrated in a proof of-concept study (Haslam et al., 2016), but it has yet to be systematically trialled. This randomised controlled trial of G4H will recruit 130 adults presenting with psychological distress (i.e., elevated symptoms of depression or a mental health diagnosis) due to social isolation who will be randomly assigned to G4H or to a wait list control. The primary outcome against which the intervention will be assessed is loneliness and secondary outcomes include depression, social anxiety, and multiple group membership. We hypothesize a greater reduction in loneliness, depression, and anxiety and increase in multiple group membership for those receiving G4H compared to the wait list control.
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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 Catherine Haslam
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Address
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School of Psychology
University of Queensland
St Lucia, Qld, 4072
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Country
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Australia
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Phone
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+ 61 (7) 3466 7565
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Fax
78846
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+ 61 (7) 3365 4466
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Email
78846
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[email protected]
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Contact person for public queries
Name
78847
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Catherine Haslam
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Address
78847
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School of Psychology
University of Queensland
St Lucia, Qld, 4072
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Country
78847
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Australia
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Phone
78847
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+ 61 (7) 3466 7565
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Fax
78847
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+ 61 (7) 3365 4466
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Email
78847
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[email protected]
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Contact person for scientific queries
Name
78848
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Catherine Haslam
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Address
78848
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School of Psychology
University of Queensland
St Lucia, Qld, 4072
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Country
78848
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Australia
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Phone
78848
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+ 61 (7) 3466 7565
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Fax
78848
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+ 61 (7) 3365 4466
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Email
78848
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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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