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A Population Based Linked Data Analysis Of The Prognostic Determinants Of Out Of Hospital Cardiac Arrest
Funder
National Health and Medical Research Council
Funding Amount
$174,000.00
Summary
Heart disease, resulting in a cardiac arrest, is the largest single cause of death for men and women in Australia, accounting alone for almost a quarter of all deaths. Despite the scope of the problem, there is a paucity of objective data about the factors that determine outcomes in the short-term and long-term. This study will capitalise on the unique research potential of the WA Data Linkage Project to combine the WA Cardiac Arrest Register with existing health service data and death records, ....Heart disease, resulting in a cardiac arrest, is the largest single cause of death for men and women in Australia, accounting alone for almost a quarter of all deaths. Despite the scope of the problem, there is a paucity of objective data about the factors that determine outcomes in the short-term and long-term. This study will capitalise on the unique research potential of the WA Data Linkage Project to combine the WA Cardiac Arrest Register with existing health service data and death records, to describe the outcomes of out-of-hospital cardiac arrest in Perth WA. Both morbidity and mortality will be described and compared to patients with similar health conditions, but who do not experience a cardiac arrest. More specifically this study will address questions such as 'what is the effect of age, gender, pre-existing illness and socio-economic status on survival from out-of-hospital cardiac arrest?' and What is the long-term survival and health status for initial survivors of out-of-hospital cardiac arrest?' This project will both identify those factors associated with best outcome as well as identify a profile of persons who are 'at risk' of experiencing a further cardiac arrest. Such information is important for the evaluation of current resuscitative practices as well as providing the basis for future planning initiatives.Read moreRead less
M-SAKHI : Mobile Health Solutions To Help Community Providers Promote Maternal And Infant Nutrition And Health - A Community-based Cluster Randomized Controlled Trial In Rural India
Funder
National Health and Medical Research Council
Funding Amount
$2,379,427.00
Summary
The proposed research will examine the impact of the mobile phone counselling on child feeding practices, & undernutrition & cognitive development in a rural setting in India. The study aims to collect high-level evidence of whether mobile phone counselling about nutrition in pregnancy, and child feeding, directed at pregnant women and mothers in rural India will i) reduce low birthweight, ii) improve infant & child feeding, and iii) reduce child undernutrition at 24 months.
Long Term Impact Of A Community-based Cluster Randomized Controlled Trial Of Peer Counselling To Improve Infant Feeding On Growth & Cognitive Function Of Children Up To 5 Years In Urban Bangladesh
Funder
National Health and Medical Research Council
Funding Amount
$851,345.00
Summary
Bangladesh still faces high levels of inappropriate infant feeding leading to child undernutrition and delayed development. Effective programs are urgently needed to help reduce undernutrition and improve child development. This study in poor urban communities in Dhaka, Bangladesh will see if long-term counseling provided by local women to mothers about appropriate infant feeding can improve child’s nutritional status, growth and cognitive function in their children at 5 years.
Investigating Early Life Exposure To Plastic Products In Australia And Subsequent Neurodevelopmental Effects
Funder
National Health and Medical Research Council
Funding Amount
$791,376.00
Summary
Child neurodevelopment disorders like autism are becoming more common. Recent work indicates almost all pregnant mothers in Australia harbour plastic chemicals – bisphenols and phthalates and foetus is also exposed. Human evidence is emerging that higher exposure to plastics during pregnancy may be associated with these disorders. Randomised controlled trials are not possible so high quality birth cohort studies, as proposed here, are required to investigate this issue comprehensively.
Early Introduction Of Dietary Allergen To Reduce The Population Prevalence Of Infant Food Allergy
Funder
National Health and Medical Research Council
Funding Amount
$412,468.00
Summary
Australia has the highest recorded prevalence of childhood peanut allergy, a potentially life-threatening condition. New evidence shows introducing peanut into the diet in infancy can reduce the risk of developing peanut allergy in high risk infants, and allergy prevention guidelines now recommend giving peanut before 12 months. This study will evaluate how effective these guidelines have been in promoting earlier peanut introduction and reducing the population prevalence of peanut allergy.
Genetic, Family And Social Determinants Of The Burden And Outcome In Rett Syndrome: A Population-based Investigation
Funder
National Health and Medical Research Council
Funding Amount
$332,550.00
Summary
Rett syndrome is a severe disorder of the nervous system mainly affecting females. At birth children with Rett syndrome often seem normal but in their second year lose skills. With time it becomes clear that they are severely intellectually and physically handicapped. In 1999 the link between Rett syndrome and a mutation in the gene, known as MECP2, was found. In Australia since 1993, we have had a register of basic information on all girls and young women diagnosed with Rett syndrome. Over thre ....Rett syndrome is a severe disorder of the nervous system mainly affecting females. At birth children with Rett syndrome often seem normal but in their second year lose skills. With time it becomes clear that they are severely intellectually and physically handicapped. In 1999 the link between Rett syndrome and a mutation in the gene, known as MECP2, was found. In Australia since 1993, we have had a register of basic information on all girls and young women diagnosed with Rett syndrome. Over three quarters of the register s 248 cases have now been genetically tested. In 2000 and again in 2002, extra information on ability to do everyday tasks, behaviour, hand function, medical conditions, and use of health and education services was collected. In 2002 questions on family well being were also included. From 2004 to 2007, further information will be gathered on function, health and well being of the affected child and their family. This will be by telephone interview, questionnaire, video recording, existing medical records, clinical assessments and tests. This will include in 2004 completion of calendars which will provide information needed to estimate health and medical care costs for these children. Similar information by questionnaire and calendar will also be collected from the parents of children with Down syndrome in 2004. The information will be used to compare the social and financial burden of Rett syndrome with Down syndrome, a commoner cause of intellectual disability. The research will also show if it is possible to predict from early genetic test results how severely a child with Rett syndrome will later be affected. It will also determine whether some ways of management improve the long-term outlook for the girl and her family. Finally this study will investigate why some families cope better with this devastating disorder than others. This research is only possible in Australia because of the ongoing register we have set up here.Read moreRead less