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Intimate partner violence (IPV) and reproductive coercion (RC) can result in serious psychological, social and physical harm. Screening patients for IPV/RC has the potential to identify and assist patients who may not otherwise discuss this with a health practitioner. Targeted screening for those with a range of specific presentations including many sexual and reproductive health issues has been recommended, but universal screening has not.The implementation and evaluation of a screening program for IPV and RC in an urban sexual and reproductive health clinic is described.The program enabled patients who had been exposed to IPV and/or RC to receive assistance and support. Screening was highly acceptable to patients, and the reception and clinical staff became both highly supportive of screening and increasingly confident to assist patients who were exposed to IPV and/or RC. Conclusion and implications for public health: This program could be adapted for use in a number of healthcare settings and lead to positive health outcomes.

Background: Indigenous children in colonised nations experience high rates of health disparities linked to historical trauma resulting from displacement and dispossession, as well as ongoing systemic racism. Skin infections and their complications are one such health inequity, with the highest global burden described in remote-living Australian Aboriginal and/or Torres Strait Islander (hereafter respectfully referred to as Aboriginal) children. Yet despite increasing urbanisation, little is known about the skin infection burden for urban-living Aboriginal children. More knowledge is needed to inform service provision, treatment guidelines and community-wide healthy skin strategies. In this pilot study we aimed to test the feasibility and design of larger multi-site observational studies, provide initial descriptions of skin disease frequency and generate preliminary hypotheses of association. Methods: This project has been co-designed with local (Noongar) Elders to provide an Australian-first description of skin health and disease in urban-living Aboriginal children. In collaboration with an urban Aboriginal Community Controlled Health Organisation (Derbarl Yerrigan Health Service), we conducted a week-long cross-sectional observational cohort study of Aboriginal children (0–18 years) recruited from the waiting room. Participants completed a questionnaire, skin examination, clinical photos, swabs and received appropriate treatment. We assessed the feasibility and impact of the pilot study. Results: From 4–8 October 2021, we recruited 84 Aboriginal children of whom 80 (95%) were urban-living. With a trusted Aboriginal Health Practitioner leading recruitment, most parents (or caregivers) who were approached consented to participate. Among urban-living children, over half (45/80, 56%) of parents described a current concern with their child’s skin, hair and/or nails; and one third (26/80, 33%) reported current itchy skin. Using a research-service model, 27% (21/79) of examined urban-living participants received opportunistic same-day treatment and 18% (14/79) were referred for later review. Conclusions: This co-designed pilot study to understand skin health in urban-living Aboriginal children was feasible and acceptable, with high study participation and subsequent engagement in clinical care observed. Co-design and strong involvement of Aboriginal people to lead and deliver the project was crucial. The successful pilot has informed larger, multi-site observational studies to more accurately answer questions of disease burden and inform development of healthy skin messages for urban-living Aboriginal children.

Context In Australia, one woman is murdered by a partner every 9 days and 26,000 children are homeless every year due to domestic violence. Consumer-centred, cost-effective violence prevention programs are urgently needed. Research indicates those exposed to violence want to be asked about it. However, clinicians find it too awkward and too time-consuming. As a result, questions are not asked and the exposure to violence continues. Our aim is to design and implement an innovative screening program for partner violence that is acceptable to both consumers and health staff, transferable to other settings and sustainable into the future. Process 1) developed screening and risk assessment tools, validated by consumers and health staff; 2) developed referral pathways; 3) trained staff; 4) modified clinic layout to be consumer-centred; 5) implemented program at Sexual Health Quarters; 6) collected staff and consumer feedback before and after implementation. Analysis quantitative analysis of 1) prevalence of violence; 2) characteristics of survivors; 3) support required; 4) staff and consumer feedback. Outcomes In the first 6 months of the program we screened 1500 women, identified exposure to violence in 18% and provided counselling to 40% of those exposed. All consumers and staff surveyed supported this program, with 90% of staff admitting that it was easier than expected. Learning Outcomes Our program highlights the feasibility and acceptability of an intervention for the secondary prevention of partner violence. A wider roll out of this program would directly contribute to the achievement of 6 out of the 17 Sustainable Development Goals.