Objective To investigate the impact of a long-term nurse home visiting programme, embedded within a universal child health system, on the health, development and well-being of the child, mother and family.
Design Randomised controlled trial.
Setting/participants 208 (111 intervention, 97 comparison) eligible at-risk mothers living in a socioeconomically disadvantaged area in Sydney, booking into the local public hospital for confinement.
Intervention A sustained and structured nurse home visiting antenatal and postnatal parenting education and support programme.
Control Usual universal care.
Main outcome measures The quality of the home environment for child development (12–24 months), parent–child interaction and child mental, psychomotor and behavioural development at 18 months.
Results Mothers receiving the intervention were more emotionally and verbally responsive (HOME observation) during the first 2 years of their child's life than comparison group mothers (mean difference 0.5; 95% CI 0.1 to 0.9). Duration of breastfeeding was longer for intervention mothers than comparison mothers (mean difference 7.9 weeks; 95% CI 2.9 to 12.9). There was no significant difference in parent–child interaction between the intervention and comparison groups. There were no significant overall group differences in child mental, psychomotor or behavioural development. Mothers assessed antenatally as having psychosocial distress benefitted from the intervention across a number of areas.
Conclusion This sustained nurse home visiting programme showed trends to enhanced outcomes in many, but not all, areas. Specifically, it resulted in clinically enhanced outcomes in breastfeeding duration and, for some subgroups of mothers, women's experience of motherhood and children's mental development.
Trial registration number ACTRN12608000473369.
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Funding The trial was funded by the Australian Research Council (LP0560285), Sydney South West Area Health Service, the NSW Department of Community Services and the NSW Department of Health.
Competing interests None.
Ethics approval The trial received approval from both the Sydney South West Area Health Service (Western Zone) and the University of NSW Human Ethics Committees.
Provenance and peer review Not commissioned; externally peer reviewed.
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