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Pain and Emotion Therapy for Chronic Low Back Pain (PaET+)
Expand descriptionA recent trial (ACTRN12622000113752) with 89 participants demonstrated the efficacy and safety of an online group-based therapy for people with chronic pain, Pain and Emotion Therapy plus TAU (PaET plus TAU). Results showed significant improvements in emotion dysregulation and provided preliminary evidence for a significant reduction in pain severity, depression, anxiety, stress, sleep problems and improved wellbeing (Norman-Nott et al., 2025). The aim of the current randomised controlled trial is to evaluate the efficacy of Pain and Emotion Therapy+ plus TAU, with an additional module on pain and movement education added to the program to reduce pain severity. Secondary aims include evaluating the effects on pain disability, emotion dysregulation, depressive symptoms, anxiety symptoms, sleep quality, level of physical activity, resilience, post-traumatic stress disorder symptoms, suicide cognitions and quality of life.
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Assessing new ways of delivering heart health checks in rural populations
Expand descriptionThis project explores new, more accessible ways for people in rural areas to complete a standard heart health check. The feasibility of two new modes of delivery will be evaluated. The at home mode of delivery enables participants to self-administer a heart health check using a returnable kit. The local pharmacy mode of delivery enables participants to receive a hearth health check at their local pharmacy facilitated by the pharmacist using the same kit. Heart Health Check assessments are communicated to participants by post, and optionally by phone. The assessment advice received recommends participants who are evaluated as intermediate and high risk follow up with a GP and bring the assessment letter to their visit. The two new modes of Heart Health Check Delivery are referred to as models of care in the study protocol below. Participants who are not selected onto the Heart Health Check Study Population will be put on to a Heart Health Check Waitlist.
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Supporting childhood mental health in disasters: Evaluation of Psychological First Aid in Schools
Expand descriptionDisasters can disrupt childhood development and increase the long-term risk of mental health difficulties. Although most children and adolescents recover with appropriate support, evidence for effective interventions to protect youth mental health in disasters remains limited. This study aims to evaluate the effectiveness of Psychological First Aid in Schools (PFA-S), a school-based training program designed to prepare primary and secondary school staff to support student wellbeing during and after disasters and critical incidents. This study will provide important evidence for an accessible, scalable school-based intervention to strengthen staff capacity to provide psychosocial support to students in disasters, promoting recovery and preventing long-term psychological impacts.
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The effect of standardised pathway on the diagnosis and management of platelet-related bleeding disorders.
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Breathing control, breathlessness and sleep in chronic obstructive pulmonary disease
Expand descriptionThis trial aims to determine changes in the control of breathing in the supine posture (lying flat on your back), with bronchodilator therapy and ventilatory support and the link with breathing discomfort and sleep in people with chronic obstructive pulmonary disease. Non-invasive recordings of brain activity, termed electroencephalography, will be used to determine changes in the control of breathing that occur with change from seated to supine posture, after bronchodilator therapy and after ventilatory support via a face mask. The link between changes in the control of breathing with breathing discomfort during these conditions (assessed by questionnaire) and sleep quality (assessed by an under-mattress sensor and sleep diaries). Baseline lung function and questionnaire responses will be collected.
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PLATONIC - polyol concentrations in cerebrospinal fluid (CSF)
Expand descriptionPathological production of polyols after brain injury may be a cause for secondary neurological injury. Polyols are osmotic and neurotoxic, which may have detrimental outcomes for critically ill individuals with brain injury. This study will be a biospecimen analysis of cerebrospinal fluid in health volunteers, aiming to quantify polyol concentrations. The results will act as a control group to compare with populations studied in other trials investigating polyol production in ICU patients with traumatic brain injury, subarachnoid haemorrhage, and pain conditions.
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A comparison of how midclavicular catheters and peripherally inserted central catheters (PICCs) perform when used in adults who receive intravenous antibiotic treatment.
Expand descriptionThis study aims to compare rates of complications, dwell time and treatment completion with midclavicular catheters and peripherally inserted central catheters (PICCs). We hypothesize that in adults, midclavicular catheters (MCCs) will be associated with lower rates of complications compared with PICCs, similar rates of treatment completion, and similar dwell time.
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Early Adjunctive Vasopressin for Vasodilatory Shock - A Stepped Wedge Vanguard Feasibility Trial: The EAVES Study
Expand descriptionVasoactive drugs are amongst the most commonly prescribed medications for critically ill adult patients in intensive care units (ICU). Noradrenaline is the universally recommended first-line agent for such patients but questions remain around the timing of commencing additional (adjunctive) vasoactive medications, such as vasopressin. This study will determine whether a large-scale stepped wedge trial implementing and evaluating a strategy of using vasopressin as an early adjunctive vasopressor in the ICU is feasible. We will also collect provisional data on the physiological effects, efficacy and safety of early adjunctive vasopressin in adults receiving vasopressors in the ICU.
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Cannabidiol and vitamin E on blood flow in the brain of older adults
Expand descriptionThe world’s population is getting older, and ageing is associated with a decline in cognition and blood circulation within the brain. This means that more people will require additional care or move into aged care facilities. Studies have shown that both cannabidiol (a non-intoxicating part of the cannabis plant) and vitamin E have the ability to improve blood flow throughout the body, particularly in the brain. This is important, because our brain requires a large percentage of our blood flow to supply it with all the oxygen and energy it needs. Through a randomised controlled trial, we will investigate the effect of cannabidiol and vitamin E on brain blood vessel function to improve cognition, over 16 weeks, anticipating that it will improve blood vessel function and cognition. It is hypothesised that both cannabidiol and vitamin E will each improve cognition and in this cohort by improving cerebrovascular function, as well as improving cardiovascular function and general physiological and psychological markers of health. It is also hypothesised that the combination of cannabidiol and vitamin E will improve cerebrovascular function and cognition as well as improving cardiovascular function and general physiological and psychological markers of health, beyond what either product achieves on its own. Your participation will help us determine if cannabidiol and vitamin E could be supplements that improve brain health. This work may help benefit yourself and others within your community to increase quality of life.
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The Mind Your Mate program: A school-based randomised controlled trial to evaluate the effectiveness of combined classroom lessons and a mobile app peer support prevention intervention.
Expand descriptionAdolescence is a crucial period for prevention efforts as numerous social and biological changes confer risk for mental health and substance use challenges, which can have enduring impacts across the life course. The Mind Your Mate Program was developed with youth, education and health experts to promote peer support, encourage help-seeking and prevent mental health and substance use problems in adolescents. Building upon the success of the pilot trial, which found significant reductions in adolescent depression, the program has been expanded into a comprehensive universal, school-based program. The new program will be evaluated through a cluster-randomised controlled trial conducted across secondary schools in Australia. We hypothesise, that compared to students receiving health education as usual, students in schools allocated to the program will show improved mental health knowledge and reduced mental ill-health risk.