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Biopsychosocial Risk And Protective Factors Of Trauma Exposure In First Responders: A Longitudinal Investigation
Funder
National Health and Medical Research Council
Funding Amount
$1,137,427.00
Summary
Investigating individual differences in response to stress is crucial to improving both psychotherapy and pharmacotherapy for individuals at high risk for exposure to trauma. This world-first project will investigate pre and post-trauma psychological and biological trajectories associated with health outcomes in first-responders, contributing significantly towards our fundamental understanding of the biology of risk and resilience to trauma exposure, a key health issue.
Quantifying The Role Of Epigenetic Factors In Neurocognitive Outcomes: A Twin Study
Funder
National Health and Medical Research Council
Funding Amount
$1,516,790.00
Summary
We aim to identify the environmental factors in early life that contribute towards an individual brain development using MRI brain scans and related psychological skills measured in late childhood. We are using twins to better understand differences in their early life environments independent of genetics.
Following bereavement, 10%-15% of people suffer prolonged grief (PG) that can cause mental and physical problems for many years. This project will study community and treatment-seeking samples of bereaved people to identify trajectories of grieving, predictors of responding across time, and identify mechanisms of change in treatment of PG. This project represents a significant advance in our understanding of PG and will help reduce the burden of this condition.
Helping Family Caregivers Of Palliative Care Patients Manage Their Roles: Evaluation Of A Hospital Based Group Education
Funder
National Health and Medical Research Council
Funding Amount
$219,810.00
Summary
While most people would prefer to die at home, the reality is that about two thirds of people die in in-patient settings, such as palliative care units. A home death is more likely if family caregivers are well prepared and supported in their role. Palliative care services are expected to support family caregivers. Research shows, however, that many family caregivers lack the required information to effectively manage their role. They are also prone to suffer psychological distress while support ....While most people would prefer to die at home, the reality is that about two thirds of people die in in-patient settings, such as palliative care units. A home death is more likely if family caregivers are well prepared and supported in their role. Palliative care services are expected to support family caregivers. Research shows, however, that many family caregivers lack the required information to effectively manage their role. They are also prone to suffer psychological distress while supporting their dying relative. Caregivers have expressed a desire for structured information to better prepare them for their role, whether their dying relative is in hospital, a palliative care unit or at home. The aim of this project is to develop and evaluate an educational program offered to family caregivers who are supporting a relative who is receiving palliative care in an inpatient setting. The education program seeks to help family caregivers manage their role and to prepare them for the patient�s home care where appropriate. It is hoped that family caregivers who have attended the program will be more competent, better prepared and more informed about their caregiving role. An additional benefit from attending the program will be the opportunity for family caregivers to meet others in similar situations to themselves. Each education program will involve approximately six family caregivers; it will be conducted very soon after their relative has been admitted to the palliative care unit. The program will be of two hours duration (including time for data collection) and will be facilitated by a suitably qualified health professional. Written resources will be provided and caregivers will be given the opportunity to meet with staff from the multidisciplinary team. Referrals for scheduled consultations will be made where relevant. The program will be conducted in three sites (two in Victoria and one in Western Australia) and will be comprehensively evaluated. The caregivers who attend the program will be invited to provide feedback by completing several questionnaires designed to determine the effectiveness of the program. Group education programs of this kind have previously not been rigorously developed and tested. We seek to address this and hope to demonstrate that we can positively influence the family care giving experience.Read moreRead less
Enhancing And Integrating Addiction Neuroscience Knowledge With Clinical Practice, By Transforming The Approach To Assessment And Classification Protocols, And Improving Outcomes By Using Neurocognitive Phenotypes For Tailored Treatments
Funder
National Health and Medical Research Council
Funding Amount
$838,845.00
Summary
Brain research has reshaped the way we understand addiction, but has not yet led to more effective treatments. This Fellowship will facilitate the creation of a neuroscience- and technology-inspired research clinic that will conduct world-leading research into the fundamental underpinnings of how lifestyle and psychological interventions affect brain and mental health, as well as translate this knowledge into effective, safe and accessible treatments tailored to those affected by addiction.
Whiplash Injury: Mechanisms, Prediction And Directives For Improved Management Strategies.
Funder
National Health and Medical Research Council
Funding Amount
$772,359.00
Summary
Whiplash is a costly condition with many people developing chronic symptoms. This research aims to improve the understating of involved mechanisms, diagnosis and classification of the condition from the time of injury until either recovery or the development of persistent pain. This will facilitate the early identification of those at risk of poor recovery and will lay the foundations for the development of improved early management, particularly in primary care.
This program of research will develop and evaluate improved strategies for communication and decision making in medical testing for consumers, patients and clinicians. Better understanding about medical tests and improved interventions to support decision making will enable patients and clinicians make more informed and more appropriate decisions about when and when not to test. This work forms part of a broader objective to build health literacy and shared health decision making in Australia.
Psychosocial Aspects Of Genomic Testing For Breast Cancer Risk
Funder
National Health and Medical Research Council
Funding Amount
$108,902.00
Summary
Assessing a woman’s breast cancer risk by profiling polygenic risk represents a new approach in the familial cancer setting. My study is part of a program of research that aims to facilitate translation of polygenic risk information into clinical practice. For this, I will invite 400 women to receive their personal polygenic result and i) assess interest in receiving this result; ii) assess psychological and behavioural outcomes of receiving or not receiving their personal polygenic risk result
Banking On The Future: Establishing Evidence For Policy, Protocols, And Patient Care Relating To Storage Of Reproductive Material Before Treatment For Cancer
Funder
National Health and Medical Research Council
Funding Amount
$588,023.00
Summary
Cancer treatment can cause infertility. Patients may freeze sperm, eggs, embryos, or ovarian tissue before cancer treatment for later use in fertility treatment. There are no national guidelines specific to this procedure, no generally accepted policies for services, inadequate knowledge about its outcomes, and limited understanding of the needs and expectations of patients who undergo it. This research will address these knowledge gaps and thus contribute to the wellbeing of cancer patients and ....Cancer treatment can cause infertility. Patients may freeze sperm, eggs, embryos, or ovarian tissue before cancer treatment for later use in fertility treatment. There are no national guidelines specific to this procedure, no generally accepted policies for services, inadequate knowledge about its outcomes, and limited understanding of the needs and expectations of patients who undergo it. This research will address these knowledge gaps and thus contribute to the wellbeing of cancer patients and survivors.Read moreRead less