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ew technology for new parents: Using technology to help parents bond with and care for their new baby

Not Applicable
Recruiting
Conditions
Pregnancy
Postpartum problems
Depression
Child bonding and attachment
Parenting Problems
Infant Development
Mental Health - Other mental health disorders
Public Health - Health service research
Reproductive Health and Childbirth - Childbirth and postnatal care
Mental Health - Depression
Registration Number
ACTRN12622000287730
Lead Sponsor
The University of Adelaide
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

< 24 weeks pregnant
Singleton pregnancy
Identified at the antenatal booking appointment as being at moderate psychosocial risk.

Exclusion Criteria

Fetal abnormality identified at morphology (approx. 18 - 20 week) ultrasound
Reporting current domestic violence
Illicit drug use
Severe mental health issues
Requiring interpreter/lack of sufficient English skills to complete questionnaires
No internet access on a mobile phone, tablet, or computer
Clinician exclusion

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Antenatal attachment measured by the maternal antenatal attachment scale (MAAS).<br><br>The online outcomes questionnaire described above will be sent to all randomised women approximately 36-38 weeks gestation, with the exception of women with severe adverse outcomes (e.g. fetal death).<br>[36-38 weeks gestation];Antenatal reflective functioning measured by the prenatal parenting reflective functioning questionnaire (P-PRFQ).<br><br>The online outcomes questionnaire described above will be sent to all randomised women approximately 36-38 weeks gestation, with the exception of women with severe adverse outcomes (e.g. fetal death)..[36-38 weeks gestation<br><br>];Parenting competence and attachment measured by parenting stress index (PSI-IV) parent domain subscales.<br><br>The online outcomes questionnaire described above will be sent to all randomised women approximately 2 months postnatal, with the exception of women with severe adverse outcomes (e.g. fetal or neonatal death).[2 and 6 months postnatal]
Secondary Outcome Measures
NameTimeMethod
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