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Does progesterone support in luteal phase deficiency help subfertile couples achieve a pregnancy?
Expand descriptionThis project aims to assess the effectiveness of progesterone as luteal phase support in unexplained subfertile women with a previously diagnosed luteal phase hormonal deficiency. All women will be instructed in a fertility awareness-based charting method (the Sympto-Thermal method). It is hypothesised that progesterone given as luteal phase support increases the likelihood of pregnancy in unexplained subfertile women with a recognised luteal phase hormonal defect.
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Does monitoring fertile times of the menstrual cycle help subfertile couples achieve a pregnancy?
Expand descriptionThis project will assess the effectiveness of a fertility awareness-based charting method in increasing the likelihood of pregnancy in a population with unexplained subfertility. It is hypothesised that the Sympto-Thermal Method increases the likelihood of pregnancy in the unexplained ovulating subfertile population.
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The Direct Benefit of Neuropsychological Assessment with Feedback in Multiple Sclerosis
Expand descriptionCognitive impairment is one of the most common symptoms in multiple sclerosis (MS), being objectively confirmed on neuropsychological assessment in at least 50% of patients. It can be functionally disabling, and has been shown to significantly impact on patients’ capacity to function in a most domains of life, including personal self-care, mental health and mood, relationships, social and leisure activities, rehabilitation, driving, and employment. Cognitive impairment can also impact upon families and caregivers. In particular, MS patient cognitive impairment has been found to be significantly associated with caregiver distress, quality of life, and caregiver strain. The rehabilitation of cognitive impairment in MS is still in its infancy, and although neuropsychological assessment is often described as the first step in the rehabilitation of cognitive impairment, it can also be a form of therapeutic intervention in its own right. However, research into the direct therapeutic benefit of neuropsychological assessment as a rehabilitative intervention in MS is very limited. So, using an RCT approach, the present study aims to investigate the direct psychological benefit of neuropsychological assessment with feedback in patients with MS and their main caregivers immediately following the feedback session and up to 10 weeks later. It is proposed that the intervention will lead to an increase in patient and caregiver knowledge of the patient’s cognitive strengths and weaknesses, to an improvement in the patient’s use of adaptive psychological strategies for coping with the health problems caused by MS, and to more positive caregiving outcomes for the caregiver.
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Seasonal Variation in Postural Balance in Community Dwelling Older Adults in Tasmania
Expand descriptionBalance impairment is an important fall risk factor and increases in range in postural sway in the medio-lateral direction in older adults are associated with increased fall risk and rates. Multivariate analysis reveals serum vitamin D levels as an independent variable associated with postural sway. In individuals with suboptimal levels of vitamin D, postural sway improves after supplementation, independently of changes to fall rate or number of people falling. Both epidemiological and longitudinal studies have shown that vitamin D levels show seasonal variation. Lowest levels of serum vitamin D are recorded towards the end of winter, approximately four weeks after the shortest day of the year. Fall rates have been shown to decrease post supplementation with vitamin D in older adults with insufficient levels (between 22 and 49nmol/L) (RaR 0.72, 95% CI 0.55 to 0.95). As vitamin D varies seasonally, and is related to postural sway, this study investigates whether postural sway varies seasonally and is related to seasonal changes in vitamin D or fall rate.
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Fish oil supplementation as adjunct therapy for chronic obstructive pulmonary disease (COPD): A feasibility study
Expand descriptionChronic obstructive pulmonary disease (COPD) is a debilitating condition that results from inflammation of the airways. This inflammation impairs lung function and thus reduces an individuals’ ability to undertake physical activities, including activities of daily living. Long-chain omega-3 polyunsaturated fatty acids (LCn-3PUFA) have been shown in a number of studies to elicit anti-inflammatory effects. People with COPD will be supplemented with either LCn-3PUFA or placebo; effects on inflammation, lung and physical function will be assessed at four months. It is anticipated that supplementation with LCn-3PUFA will reduce inflammation, and improve physical function (exercise capacity), which will collectively improve health related quality of life
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Effects of L-DOPS in Patients with Low- and Normal- Blood Pressure Variants of Orthostatic Intolerance.
Expand descriptionDifficulty in maintaining the upright posture is called Orthostatic Intolerance. Orthostatic Intolerance may result in fainting or symptoms such as light-headedness, blurred vision, nausea and palpitations. These symptoms come on when standing or sitting, particularly for prolonged periods or time or in warm weather, and are relieved by lying down. They are often associated with an abnormal blood pressure or heart rate response to sitting or standing. Our research to date has looked in detail at two clinical groups with these symptoms. Both of these groups have overall normal nervous system function, but with intermittent difficulty in maintaining the upright posture. One group always has very low blood pressure (Low Supine Blood Pressure Orthostatic Intolerance) and the other normal blood pressure (Normal Supine Blood Pressure Orthostatic Intolerance). Our studies have particularly looked for differences in the way a part of the nervous system called the sympathetic nervous system responds to the upright posture in these two groups when compared to healthy control participants. The sympathetic nervous system, the stimulant arm of the nervous system is responsible for our “flight and fight” response to a threatening situation. The sympathetic nervous system is also crucial in the control of blood pressure and allows us to stand upright and supply blood to our vital organs, including the brain, in the face of gravity that pulls blood towards our legs. We have found that people with these two forms of Orthostatic Intolerance do not release as much of the main chemical messenger of the sympathetic nervous system – called noradrenaline - into their circulation in response to upright posture when compared with healthy control participants. We have found distinct differences between these two groups and between each group and healthy control participants in the processing pathways for noradrenaline. Current medical treatments for these forms of Orthostatic Intolerance have focused on increasing blood volume by increasing dietary salt or by the use of a medication (Fludrocortisone) that make the body retain salt and fluid. In addition medications that act to tighten blood vessels with standing (Midodrine or Dihydroergotamine) may also be used. These medications can be very helpful for some patients but are often not tolerated due to side effects and many patients continue to experience symptoms even with these medications. None of these medications has been proven to be of benefit in randomised trials to date. This trial will be comparing a new treatment – L-DOPS (Droxidopa) – with placebo (a tablet that appears the same as the L-DOPS tablets but contains no active ingredients) in patients with the two forms of Orthostatic Intolerance described above. L-DOPS is a nerve transmitter precursor that is converted by the body to noradrenaline, the main nerve messenger of the sympathetic nervous system. L-DOPS is an experimental treatment. This means it is not approved for patients with Low- or Normal- supine blood pressure Orthostatic Intolerance in Australia or other parts of the world. L-DOPS has been marketed in Japan since 1989 for use in patients with Parkinson Disease and Orthostatic Intolerance. L-DOPS remains an investigational drug in the United States and Australia. Current trials in the United States and Canada are studying its benefit in blood pressure regulation disorders in Parkinson disease and in symptoms in patients with Chronic Fatigue syndrome and Fibromyalgia (a condition associated with painful muscles). This study will include: 20 Healthy control Participants 28 Participants with Low supine Blood Pressure Orthostatic Intolerance 28 Participants with Normal Supine Blood Pressure Orthostatic Intolerance All participants will be studied through the Alfred Baker Medical Unit at the Alfred Hospital The purpose of this research is twofold: 1. The baseline assessment will compare the way the sympathetic nervous system responds to the ‘stress’ of the upright posture in healthy control participants and participants with the two different clinical presentations of Orthostatic Intolerance described above. These responses will be correlated with the individual pattern of nerve proteins and nerve transmitter levels - obtained from a forearm vein biopsy- in the participants. This part of the study is to being performed to confirm our previous findings in a larger group of participants and to provide baseline measurements for the participants with Orthostatic Intolerance who will participate in the second phase of the study. 2. The second phase of the study is to assess whether the nerve transmitter replacement L-DOPS(Droxidopa) is able to improve symptoms and normalise the sympathetic nervous system response to upright posture in participants with the low- and normal- supine blood pressure variants of Orthostatic Intolerance.
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A randomised controlled trial to evaluate paediatric critical care telemedicine in Queensland
Expand descriptionIn Queensland, facilities for seriously ill children are centralised in Brisbane. The Paediatric Intensive Care Unit (PICU) at the Royal Children's Hospital provides advice and retrieval services for children who have presented at rural and regional hospitals throughout Queensland. When advice is needed, it is provided by telephone and this relies on the ability of the remote clinician to provide a good verbal description of the patient and an accurate interpretation of paediatric x-rays. Clinicians at the remote hospital may be relatively inexperienced at caring for critically ill children. Support from the PICU is essential. Telemedicine allows clinicians to hold a consultation at a distance by video. In addition to face-to-face communication, telemedicine may be used to view the patient, the monitors and x-rays - as if present in the same room. The addition of visual information offers the potential for a much richer dialogue than is possible by telephone alone. Alongside high-quality local care and a well co-ordinated retrieval service, telemedicine may be a potentially useful tool. This is a new area of research and very little has been reported in the literature. A limited number of studies in the USA have shown that telemedicine assists in the management of seriously ill children at a distance. Over a three year period, this study will formally evaluate the use of telemedicine to provide critical care support from the RCH PICU to four regional hospital emergency departments. The study will provide evidence on the feasibility, clinical usefulness and economics of the approach within the Queensland context. The following hypotheses will be tested: Efficacy Paediatric critical care consultation by telemedicine will: (i) improve patient condition between initial call and retrieval team arrival; (ii) reduce the time needed by the retrieval team to stablise the patient before transport; (iii) reduce diagnostic discordance; (iv) reduce the number of retrieved patients admitted to general wards; (v) improve 30 day mortality. Economics Paediatric critical care telemedicine is economically beneficial from the health service perspective reducing the number and therefore cost of retrieval and unnecessary tertiary admission.
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Emotional Engagement Treatment for Disruptive Children with Callous-Unemotional Traits
Expand descriptionThis study aims to evaluate the efficacy of a new treatment for disruptive children with callous-unemotional traits. The treatment is called 'Emotional Engagement' Treatment, and focuses on the affective dimension of parent-child relations. It has been created specifically to boost warmth in parent-child relationships, and remediate deficits in eye contact by enhancing the salience of the eyes for high CU children. The aims of the treatment are twofold – to increase parental warmth and to increase the child’s attention to parental warmth. It is believed that improvements in these areas will translate to reductions in disruptive and antisocial behavior. It is hypothesised that following treatment: 1. Children will show lower levels of disruptive behaviour 2. Children will show higher levels of eye contact 3. There will be higher levels of parental warmth
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Evaluation of ocular health and comfort in non spectacle wearer and non contact lens wearers (emmetropes) for three months
Expand descriptionThe results from this study will allow for further understanding of the ocular surface response and subjective comfort responses of the emmetropic population. The insight into the subjective comfort responses of this population can further enhance knowledge in the subjective comfort responses of the spectacle and contact lens wearing populations. The hypothesis of this study is that there will be no difference in ocular health and comfort in emmetropes over the course of three months.
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Evaluation of ocular health and comfort of spectacle wearers for three months
Expand descriptionThe results from this study will allow for further understanding of the ocular surface response and subjective comfort responses of the spectacle wearing population. By understanding spectacle wearer responses, it may contribute to the knowledge of the causes of discomfort in the contact lens wearing population. The hypothesis of the study is that there will be no difference in the ocular health and subjective comfort of spectacle wearers over the course of three months.