Publications
Below is a selection of our publications.
Impact of COVID-19 restrictions on people with hypertension – Carissa Bonner et al (Preprint)
It is unclear how people with hypertension are responding to the COVID-19 pandemic given their increased risk, and whether targeted public health strategies are needed. This retrospective case-control study compared people with hypertension to matched healthy controls during COVID-19 lockdown, to determine whether they have [...]
Behavioural barriers to COVID-19 testing in Australia – Carissa Bonner et al (Preprint)
The current suppression strategy for COVID-19 in Australia is dependent on people getting tested and self-isolating while they have COVID-19 symptoms. However, there is very little research on the behaviours and behavioural barriers involved in getting tested, both in Australia and worldwide, despite there being [...]
Views of healthcare professionals about the role of Active Monitoring in the management of Ductal Carcinoma in Situ (DCIS): qualitative interview study – Brooke Nickel et al
This study highlights the important need for robust randomised controlled trial data about active monitoring for women with low-risk DCIS, to provide HCPs with confidence in their management recommendations and decision-making.
Variations in outcomes for women admitted to hospital in early versus active labour: an observational study – Yvette Miller, Rachel Thompson et al
There is no available evidence for the prevalence of early labour admission to hospital or its association with rates of intervention and clinical outcomes in Australia. The objectives of this study were to: estimate the prevalence of early labour admission in one hospital in Australia; [...]
Lessons from the COVID-19 pandemic: People’s experiences and satisfaction with telehealth during the COVID-19 pandemic in Australia – Jennifer Isautier et al (Preprint)
This study has shown that telehealth appointments were reported to be comparable to traditional in-person medical appointments by most of our sample. Telehealth should continue to be offered as a mode of healthcare delivery while the pandemic continues and may be worthwhile beyond the pandemic.
Clinician and patient beliefs about diagnostic imaging for low back pain: a systematic qualitative evidence synthesis – Sweekriti Sharma et al
Overuse of diagnostic imaging for patients with low back pain remains common. The underlying beliefs about diagnostic imaging that could drive overuse remain unclear. We synthesised qualitative research that has explored clinician, patient or general public beliefs about diagnostic imaging for low back pain.
Protocol for a systematic review of qualitative and quantitative effects of cardiovascular disease risk communication using heart age concepts – Carissa Bonner et al (Preprint)
The concept of heart age is increasingly used for health promotion and alongside clinical guidelines for cardiovascular disease (CVD) prevention. These tools have been used by millions of consumers around the world, and many health organisations promote them as a way of encouraging lifestyle change. [...]
Future directions in cardiovascular disease risk prediction – Jenny Doust, Carissa Bonner, Katy Bell (invited analysis)
Although the National Vascular Disease Prevention Alliance (NVDPA) guidelines were published in 2012, many individuals at high risk of cardiovascular disease (CVD) are not prescribed preventive medication or have CVD risk factors recorded. Better use of CVD risk prediction tools and targeting of medication could [...]
Experiences of a national web-based heart age calculator for cardiovascular disease prevention: User characteristics, heart age results, and behaviour change survey – Carissa Bonner et al
Heart age calculators are used worldwide to engage the public in cardiovascular disease (CVD) prevention. Experimental studies with small samples have found mixed effects of these tools, and previous reports of population samples that used web-based heart age tools have not evaluated psychological and behavioural [...]
Supporting patients to be involved in decisions about their health and care: Development of a best practice health literacy App for Australian adults living with Chronic Kidney Disease – Danielle Muscat et al
Inadequate health literacy is common in those with chronic kidney disease (CKD), especially among culturally and linguistically-diverse groups. Patient information for people with CKD, including those with kidney failure requiring dialysis, is often written beyond their literacy level, and many CKD-related apps are not accurate [...]