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Trial registered on ANZCTR
Registration number
ACTRN12613000660785
Ethics application status
Approved
Date submitted
16/04/2013
Date registered
17/06/2013
Date last updated
24/06/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effectiveness of Triple P - Positive Parenting Program for Chinese parents in Mainland China
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Scientific title
A randomized-controlled trial of Triple P - Positive Parenting Program for Chinese parents who are worried about children's academic learning to improve their parenting and children's academic behaviors
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Secondary ID [1]
282342
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Nil
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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:
Parenting practices
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child emotional and behavioral problems
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child academic self-regulation and learning stress
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Condition category
Condition code
Mental Health
289234
289234
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0
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Studies of normal psychology, cognitive function and behaviour
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Public Health
289235
289235
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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
An intervention of Group Triple P will be delivered as group training and telephone consultations, which teaches parents parenting strategies to develop desirable relationship with child, to promote child positive behaviors and to manage child difficult behaviors. Participating parents will be assigned randomly to two groups, intervention group and waitlist control group. The intervention group will immediately receive the Group Triple P training, which will last for 8 weeks, while the waitlist group will receive the same training afterwards. The Group Triple P intervention includes 8 sessions, with 4 x 2 hours group training which will be provided in the first four weeks, and then 4 X 15-30 minutes telephone consultations for the later 4 weeks. Session attendance will be recorded to monitor parents' adherence. The program will be provided by a trained practitioner in Chinese.
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Intervention code [1]
286959
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Behaviour
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Comparator / control treatment
The comparator for the intervention group is a waitlist control group,which will receive the same Group Triple P training once the intervention group have completed the program.
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Control group
Active
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Outcomes
Primary outcome [1]
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Parent outcome1: Parenting practices as measured by the Parenting and Family Adjustment Scale (PAFAS) and Alabama Parenting Questionnaire (APQ).
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Assessment method [1]
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Timepoint [1]
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Pre-intervention, Post-intervention, and 6-month follow-up.
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Primary outcome [2]
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Parent outcome2: Parent involvement, as measured by Family Involvement Questionnaire.
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Assessment method [2]
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Timepoint [2]
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Pre-intervention, Post-intervention, and 6-month follow-up.
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Primary outcome [3]
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child outcome:
Academic self-regulation as measured by Academic Self-Regulation Questionnaire.
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Assessment method [3]
289375
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Timepoint [3]
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Pre-intervention, Post-intervention, and 6-month follow-up.
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Secondary outcome [1]
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Client satisfaction, as measured by Client Satisfaction Questionnaire.
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Assessment method [1]
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Timepoint [1]
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Post-intervention
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Secondary outcome [2]
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Child behavioral and emotional problems, as measured by Child Adjustment and Parenting Efficacy Scale.
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Assessment method [2]
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Timepoint [2]
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Pre-intervention, Post-intervention and 6 months follow-up.
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Secondary outcome [3]
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Parenting efficacy, as measured by Child Adjustment and Parenting Efficacy Scale
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Assessment method [3]
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Timepoint [3]
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Pre-intervention, Post-intervention, 6 months follow-up.
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Secondary outcome [4]
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Learning stress, as measured by Educational Stress Questionnaire.
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Assessment method [4]
303306
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Timepoint [4]
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Pre-intervention, Post-intervention and 6 months follow-up.
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Eligibility
Key inclusion criteria
(1) Parents are currently living together with their children;
(2) Parents need to report being worried about child's academic learning;
(3) Child of parents is studying in grade 1 - 3 of primary schools;
(4) Parents are literate in Chinese and can read and write Chinese.
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Minimum age
25
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
(1)Parents or carers having a child with health problems or disabilities (including intellectual and learning disabilities);
(2)Parents or carers do not live currently with their child;
(3)Parents or carers are currently receiving on-going support from other programs or professionals in regards to their child's learning.
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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)
Parents will voluntarily participate in the study. Their eligibility will be assessed by the research team over the telephone. After parents receive a brief explanation of the study and indicate verbal consent to participate, a package of questionnaires (pre-intervention assessment) will be sent to them via internet or mail. After they complete the questionnaires, parents will be randomly assigned to intervention group or waitlist control group.
The procedure for the treatment allocation: A person who is not involved in the trial will generate the treatment allocation sequence with a lists of computer-generated random numbers. The person then will record this in a folded piece of paper and place it in sequentially numbered, sealed and opaque envelopes. Once parents have completed the pre-intervention assessment, the researcher will open the sealed envelope and informed parents their allocation.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A computer-generated list of random numbers will be used to assign the participants to 2 groups.
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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
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
25/03/2013
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Actual
1/04/2013
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Date of last participant enrolment
Anticipated
25/04/2013
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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
80
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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China
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State/province [1]
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Shanghai
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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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The University of Queensland
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Address [1]
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School of Psychology,
The University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Dr Alina Morawska (The primary supervisor of Mingchun Guo)
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Address
School of Psychology,
The University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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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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Mingchun Guo
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Address [1]
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School of Psychology,
The University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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Country [1]
285877
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Matthew R. Sanders
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Address [1]
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School of Psychology,
The University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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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]
289115
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The University of Queensland Ethics Committee (Behavioural and Social Sciences Ethical Review Committee)
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Ethics committee address [1]
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Research and Innovation Division, Research Road, University of Queensland, St Lucia, QLD 4072
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Ethics committee country [1]
289115
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Australia
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Date submitted for ethics approval [1]
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23/01/2013
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Approval date [1]
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24/01/2013
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Ethics approval number [1]
289115
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2013000068
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Summary
Brief summary
Triple P - Positive Parenting Program,as the first evidence-based public health model, has been disseminated to a number of countries across various cultures. However, the effectiveness with Chinese parents in Mainland China has never been tested, yet there's no evidence-based parenting program in Mainland China. Moreover, it is also unknown if Triple P can have any effects on children's academic lives. This research project aims to test the effectiveness of a Triple P variant - Group Triple P with Chinese parents and on children's academic outcomes in Shanghai, Mainland China. A randomized control research design will be employed. It is expected that in comparison to parents in a waitlist control group, parents who receive Group Triple P training (intervention group) will report a significant increase in parenting efficacy, parental teamwork and parent involvement, and a significant decrease in dysfunctional parenting practices, parental stress, and child emotional and behavioral problems. Also the children of these parents will report significant improvement of parenting of their parents, significant increase in academic self-regulation, and significant decrease in learning stress. These changes are predicted to be maintained at 6-month follow-up assessment.
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Trial website
https://exp.psy.uq.edu.au/china/
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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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Mr Mingchun Guo
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Address
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School of Psychology,
University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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Country
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Australia
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Phone
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+61733467689
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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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Mingchun Guo
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Address
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School of Psychology,
University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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Country
39315
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Australia
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Phone
39315
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+61733467689
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Fax
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Email
39315
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[email protected]
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Contact person for scientific queries
Name
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Mingchun Guo
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Address
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School of Psychology,
University of Queensland,
St Lucia,
Brisbane,
Qld 4072
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Country
39316
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Australia
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Phone
39316
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+61733467689
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Fax
39316
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Email
39316
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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.
Download to PDF