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The Next Generation Of Impact In Cystic Fibrosis - Adolescent Mental Health And Beyond
Funder
National Health and Medical Research Council
Funding Amount
$76,365.00
Summary
My project studies adolescents with cystic fibrosis and explore how mental health issues influence and associate with important health outcomes relating to respiratory health, sleep quality, pain issues, family functioning, financial and social status and ability to manage treatment plans. I will recruit participants from the AREST CF (Australian Respiratory Early Surveillance Team for Cystic Fibrosis) project that studies children with CF from diagnosis.
Early Origins Study Of Cystic Fibrosis-related Diabetes
Funder
National Health and Medical Research Council
Funding Amount
$128,188.00
Summary
Cystic Fibrosis is a genetic condition that causes recurrent lung infections and early death. Some patients also develop diabetes which causes a more rapid decline. Many young children with CF have “pre-diabetes” but guidelines do not recommend screening high glucose in this group. In order to intervene early, this study aims to determine if “pre-diabetes” in very young children with Cystic Fibrosis causes poorer growth, lung function or an increase in bacterial infections to.
A Prospective, Randomised, Double-blind Trial Of Extended- Versus Bolus-infusion ?-lactam Therapy In Infective Exacerbations Of Cystic Fibrosis
Funder
National Health and Medical Research Council
Funding Amount
$148,431.00
Summary
I am an infectious diseases physician focused on the most effective way to use antibiotics to treat infections. People with cystic fibrosis often get lung infections and the bacteria that causes this, Pseudomonas aeruginosa, can be difficult to treat. I will be investigating whether infusing antibiotics over a prolonged period of time is more effective than standard therapy in treatment of Pseudomonas aeruginosa lung infections in patients with cystic fibrosis.
Early Detection Of Pulmonary Exacerbation In Cystic Fibrosis Using Nocturnal Measurements Of Cough And Sleep
Funder
National Health and Medical Research Council
Funding Amount
$140,949.00
Summary
Cystic Fibrosis (CF), the most common lethal inherited disorder effecting Australians, is a medical success story, with survival increasing from 5 years in 1970 to 40 years now. However, lower respiratory tract infections remain the major problem in CF. This project will develop and test a simple, non-invasive device to detect early chest infections, allowing early treatment, improving quality of life and preventing lung scarring. Less hospitalisations will benefit both patients and hospitals.
Improving The Design Of Pragmatic Clinical Trials In Children
Funder
National Health and Medical Research Council
Funding Amount
$128,224.00
Summary
Whilst clinical research is designed to investigate interventions that improve patient health, to date, patients (including children) and their families have had no say in deciding what health outcomes matter most to them. The voices of patients and their families must be heard and used to inform how studies are designed if we are to achieve an improved model of health care and health service delivery. We propose to investigate and provide recommendations as to how this is best achieved.
The Impact Of Sleep Disturbance On Daytime Functioning, Mood And Quality Of Life In Children And Adolescents With Cystic Fibrosis.
Funder
National Health and Medical Research Council
Funding Amount
$62,146.00
Summary
Cystic fibrosis(CF) is the most common inherited chronic disease affecting Australian children. In adults with CF sleep complaints are common and associated with depression and reduced quality of life(QOL). There is a paucity of international data however regarding sleep in children with CF and assessment of paediatric sleep problems in CF is not routine. The aim of this study is to determine sleep patterns in children with CF and to examine the relationship between sleep quality, QOL and mood.
Long Term Outcomes Following Early Infection And Inflammation In Cystic Fibrosis Lung Disease
Funder
National Health and Medical Research Council
Funding Amount
$75,006.00
Summary
This study involves the long-term follow up of birth cohort of 98 infants with cystic fibrosis, with the objectives of assessing the impact of lower airway infection and inflammation in infancy and early childhood on the development of CF lung disease over 20-25 years, and of describing the development of the lower airway microbiota in early CF lung disease and its relationship to clinical outcomes.
Non-invasive Methods Of Measuring Work Of Breathing In Children
Funder
National Health and Medical Research Council
Funding Amount
$41,267.00
Summary
Sleep-disordered breathing such as obstructive sleep apnoea, is currently diagnosed if a child stops breathing more than once per hour. For children with asthma or cystic fibrosis, who may not stop breathing during the night, how hard their breathing muscles work can have a significant impact on their health. A non-invasive method of measuring respiratory effort, and incorporating this measurement into how sleep-disordered breathing is diagnosed, can revolutionize how sleep-disordered breathing ....Sleep-disordered breathing such as obstructive sleep apnoea, is currently diagnosed if a child stops breathing more than once per hour. For children with asthma or cystic fibrosis, who may not stop breathing during the night, how hard their breathing muscles work can have a significant impact on their health. A non-invasive method of measuring respiratory effort, and incorporating this measurement into how sleep-disordered breathing is diagnosed, can revolutionize how sleep-disordered breathing in children are managed world-wide.Read moreRead less
Characterising The Molecular Basis Of Cystic Kidney Diseases Using Kidney Organoids Created By Directed Differentiation Of Patient-derived, Induced Pluripotent Stem Cells.
Funder
National Health and Medical Research Council
Funding Amount
$122,714.00
Summary
Inherited genetic mutations cause almost half of chronic kidney diseases in children. In most cases we do not know what the mutation is or how it causes kidney disease. In this study we will turn skin cells from children with kidney disease into stem cells and then use these to make a mini-kidney in a dish. This will act as a model of kidney disease allowing us to understand what the problem is at the level of changes within the cells. This may result in new ways of treating kidney disease.