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Trial registered on ANZCTR
Registration number
ACTRN12613001273774
Ethics application status
Approved
Date submitted
14/11/2013
Date registered
19/11/2013
Date last updated
4/07/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Australian Father's Study: A longitudinal study of men about to become fathers and their engagement in pregnancy, birth and the early postnatal period.
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Scientific title
Australian Father's Study: A longitudinal study of men about to become fathers and their engagement in pregnancy, birth and the early postnatal period.
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Secondary ID [1]
283597
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Nil
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Universal Trial Number (UTN)
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Trial acronym
AFS
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Fatherhood
290520
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Condition category
Condition code
Reproductive Health and Childbirth
290907
290907
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0
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Normal pregnancy
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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
There is no trial intervention. This is an observational study of men's engagement in the antenatal, birth and early postnatal period. Men will complete three questionnaires. One will be completed in the third trimester (between 30 and 40 weeks of their partner's pregnancy). A second after birth (between day 0 to 5 after the birth), and a third at six weeks postnatal (between weeks five and seven postnatal).
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Intervention code [1]
288284
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Not applicable
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Comparator / control treatment
There is no intervention. This is an observational study. Within the study will be comparisons between men by
a) Employment (Hours worked per week and FIFO status versus not)
b) Race (ATSI verus not)
c) Age (teenage versus older)
d) Migrant status (born Australia versus not)
The primary outcome will be engagement measured using a set of five choices and validated internally (with correlation statistics) with a Likert scale score.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Engagement in antenatal care measured using a question with a list of options (fully engaged to fully disengaged) and internally validated using correlation coefficients against a Likert scale score of engagement.
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Assessment method [1]
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Timepoint [1]
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Third trimester
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Primary outcome [2]
290892
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Engagement in birth measured using a question with a list of options (fully engaged to fully disengaged) and internally validated using correlation coefficients against a Likert scale score of engagement.
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Assessment method [2]
290892
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Timepoint [2]
290892
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Post delivery
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Primary outcome [3]
290893
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Engagement in the first six weeks postnatal measured using a question with a list of options (fully engaged to fully disengaged) and internally validated using correlation coefficients against a Likert scale score of engagement.
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Assessment method [3]
290893
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Timepoint [3]
290893
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End of six weeks postnatal
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Secondary outcome [1]
305561
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Anxiety, depression and quality of life in pregnancy measured using the Hospital Anxiety and Depression Scale (HADS) and Satisfaction with Life Scale (SWLS)
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Assessment method [1]
305561
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Timepoint [1]
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Third trimester between weeks 30 and 40 of their partner's pregnancy
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Secondary outcome [2]
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Anxiety, depression and quality of life after birth measured using the Hospital Anxiety and Depression Scale (HADS) and Satisfaction with Life Scale (SWLS)
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Assessment method [2]
305562
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Timepoint [2]
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Following birth (between day 0 and 5 after birth)
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Secondary outcome [3]
305563
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Anxiety, depression and quality of life after six weeks postnatal measured using the Hospital Anxiety and Depression Scale (HADS) and Satisfaction with Life Scale (SWLS)
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Assessment method [3]
305563
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Timepoint [3]
305563
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Six weeks postnatal
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Eligibility
Key inclusion criteria
Male who is the acknowledged father of an unborn baby
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Minimum age
16
Years
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Maximum age
80
Years
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Sex
Males
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Not acknowledged by the pregnant woman as father of the unborn baby
Unable to speak english
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
Evaluation of factors associated with engagement
Descriptive statistics
Compare continuous variables Student t test/Mann Whitney U test
Compare discrete variables Chi Square/Fisher Exact test
Multivariate analysis of variables significantly associated with engagement on univariate analysis including all variables significant at p<0.1 in model
Sample size was determined to provide power >80% and alpha error <0.05 to assess differences in engagement of 15% between men in categories under comparison (e.g. FIFO, teenage, migrant, ATSI) from the background rate in the wider cohort assumed to be 50%. The study population was selected to ensure adequate numbers of subpopulations as well as a large comparison group. This generated a sample size of 1000.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/07/2013
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Actual
1/07/2013
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Date of last participant enrolment
Anticipated
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Actual
31/12/2016
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Date of last data collection
Anticipated
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Actual
31/12/2017
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Sample size
Target
1000
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Accrual to date
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Final
1050
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
1718
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Joondalup Health Campus - Joondalup
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Recruitment postcode(s) [1]
7560
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6027 - Joondalup
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Funding & Sponsors
Funding source category [1]
288277
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Self funded/Unfunded
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Name [1]
288277
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Professor Julie Quinlivan
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Address [1]
288277
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Suite 106
Joondalup Health Campus
Shenton Avenue
Joondalup WA 6027
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Country [1]
288277
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Australia
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Primary sponsor type
Individual
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Name
Professor Julie Quinlivan
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Address
Suite 106
Joondalup Health Campus
Shenton Avenue
Joondalup WA 6027
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Country
Australia
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Secondary sponsor category [1]
286994
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Individual
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Name [1]
286994
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A/Prof Rodney Petersen
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Address [1]
286994
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Women's and Children's Hospital
72 King William Rd
North Adelaide SA 5006
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Country [1]
286994
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290173
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Joondalup Health Campus Ethics Committee
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Ethics committee address [1]
290173
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Executive Joondalup Health Campus Shenton Avenue Joondalup WA 6027
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Ethics committee country [1]
290173
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Australia
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Date submitted for ethics approval [1]
290173
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Approval date [1]
290173
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02/05/2013
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Ethics approval number [1]
290173
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1301
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Summary
Brief summary
Prospective study of 1000 men who are the acknowledged father of an unborn baby. Men will be recruited via their partner. Following informed consent, men are followed across the antenatal period, birth and their involvement in the study concludes six weeks postpartum. Men complete an antenatal, birth and postnatal questionnaires that addresses demographic, engagement, anxiety and depression, quality of life questionnaires and in addition questionnaires specific to each stage (antenatal focuses on pregnancy issues, birth on birth issues and postnatal on issues anticipated to arise in the first six weeks postpartum).
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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 Julie Quinlivan
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Address
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Suite 106
Joondalup Health Campus
Shenton Avenue
Joondalup WA 6027
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Country
44350
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Australia
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Phone
44350
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61 8 94009631
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Fax
44350
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Email
44350
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[email protected]
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Contact person for public queries
Name
44351
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Julie Quinlivan
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Address
44351
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Suite 106
Joondalup Health Campus
Shenton Avenue
Joondalup WA 6027
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Country
44351
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Australia
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Phone
44351
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61 8 94009631
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Fax
44351
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Email
44351
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[email protected]
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Contact person for scientific queries
Name
44352
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Julie Quinlivan
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Address
44352
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Suite 106
Joondalup Health Campus
Shenton Avenue
Joondalup WA 6027
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Country
44352
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Australia
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Phone
44352
0
61 8 94009631
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Fax
44352
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Email
44352
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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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