ANZCTR search results

These search results are from the Australian New Zealand Clinical Trials Registry (ANZCTR).

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30792 results sorted by trial registration date.
  • The observation of radiotherapy doses achieved when planning on an empty bladder versus a full Bladder for prostate radiotherapy treatment.

    Aim: The aim of this study is to improve the patient experience in the future, whilst lowering the risk of planning errors, treatment errors, and the need for replanning. Who is it for: You may be eligible for this study if you are male or female age 18 or older with confirmd prostate only or prostate with SVs. Study details: Participants will receive one radiotherapy planning scan session as per the current standard of care. The extra Computed Tomography scan will be completed on the same day if the patient agrees to participate in the study. the extra scan will take approximately 20 minutes and will deliver an extra 7.6 mSv of dose. It is hoped that findings from this study will be a lower risk of patients having to miss their treatment due to the inability to reproduce the bladder size from initial planning scan. Patients will be in the department for a smaller amount of time, and it will have less of a knock-on effect to other patients receiving treatment.

  • Effect of implementing a treatable traits approach on care of high risk chronic respiratory disease (the TAPPET trial)

    Patients with chronic respiratory diseases are frequently hospitalised despite receiving the best available drug treatments. Systemic inflammation and frequent chest infections represent clinical signs (treatable traits) across multiple chronic respiratory diseases. These treatable traits are known to predict high risk of hospitalisations but are not routinely targeted by treatments. Non-drug treatments such as pulmonary rehabilitation and self-management are effective in reducing hospitalisations, but their potential to transform outcomes for high risk patients is unrealised, due to limited access and lack of guidance on optimal implementation. In this clinical trial we will implement a treatable traits approach that identifies patients at highest risk of hospitalisation, and targets personalised, safe, low-cost model of home pulmonary rehabilitation and self-management.

  • Physiotherapy management options for women who experience separation of their abdominal muscles in the first 6 months after giving birth

    The aim of this study is to determine if treatments administered by a physiotherapist are effective at reducing the gap between abdominal muscles in the first 12 weeks after giving birth in people with a separation of >28mm at the level of the belly button compared with natural recovery. Secondarily, this study aims to determine if there is a difference between participant-reported pelvic floor function, body satisfaction, back pain, pelvic girdle pain, satisfaction with outcome, and abdominal pain and/or discomfort between the three groups across the first 6 months postpartum. Force transfer across the front of the trunk will also be measured and compared between and within groups to see if improved transfer of forces across the front of the trunk is related to the width of the gap, body image, pelvic floor dysfunction, or treatment group.

  • A 2-part Phase I study to evaluate the safety, tolerability, pharmacokinetics and food effects of AXN-027

    This study in healthy volunteers aims to identify the range of safe single and multiple doses of AXN-027 Salt administered by mouth; to assess how the body handles AXN-027 Salt; how AXN-027 Salt contained in capsules compares to AXN-027 Salt contained in a tablet, what effect a high fat meal has on how the body handles AXN-027 absorption and to evaluate the safety of AXN-027 Salt compared to placebo. The results of this study will help identify appropriate doses of AXN-027 Salt to evaluate in future clinical trials.

  • A randomised controlled trial of online self-reported clinical information followed by clinical interview in mental health triaging via phone.

    The study aimed to test whether the online mental health self-report by patients at home (or anywhere with internet and phone access) without necessarily presenting to an emergency department, to inform subsequent clinical triage contributed to reduction in the time required to complete triaging e and whether this novel approach was acceptable. Study hypotheses: 1) The intervention (online mental health self-report by patients prior to triage phone interview) reduces triage time compared to the usual triaging process; 2) The intervention is acceptable to clinicians and clients.

  • Dads Tuning in to Kids: Real-world evaluation

    Dads Tuning in to Kids (Dads TIK) is an evidence-based parenting program that helps fathers to understand and regulate their own emotions and to use emotion coaching with their children to promote children’s competence. Dads TIK has been selected as one of several programs to be delivered as part of the Movember 'Scaling What Works' project, with a focus on improving men's mental health outcomes. As part of the ‘Scaling What Works’ project, 40 facilitators are trained to deliver Dads TIK to approximately 800 ‘hard to reach’ fathers. This research specifically aims to explore the acceptability, effectiveness, and adaptability of Dads TIK in this ‘real world’ context. Outcomes of interest include the impact of Dads TIK on men’s health by strengthening connections between fathers and their children, supporting emotional competence, improving fathers' responses to their children's emotions and improving father’s wellbeing in order to reduce mental health problems. More broadly, the project aims to contribute to cultural change where emotions become more acceptable for men.

  • A phase 1 safety trial of CANN001, a hydrogel patch containing 2-deoxy-D-Ribose, in diabetic foot ulcers

    Diabetic foot ulcers are a chronic wound and the pathophysiology is linked to neuropathy, infection and peripheral vascular disease. This peripheral vascular disease, linked to diabetes, prevents ulcer closure and leads to susceptibility to infection. 2-deoxy-D-ribose (2dDr) is known to promote vascularisation and may therefore increase angiogenesis when administered to a DFU and through this mechanism promote wound closure. The planned study will investigate if CANN001 (2dDr containing hydrogel) is safe in patients with diabetic foot ulcers and whether 2dDr may promote DFU healing and localised wound angiogenesis/neovascularisation through increasing local expression of VEGF.

  • Helping Women Overcome Infertility Distress: The Impact of Eye Movement Desensitization and Reprocessing (EMDR) Therapy

    This study aims to investigate the effectiveness of Eye Movement Desensitization and Reprocessing (EMDR) therapy in reducing infertility-related distress in women undergoing infertility treatments. The research will compare the emotional and psychological outcomes of women receiving EMDR therapy with those on a waitlist control group. It is hypothesised there will be differences between the groups in terms of distress, anxiety, depression, trauma-related symptoms, psychological well-being, and coping strategies. Participants will be assessed before, after, and three months post-treatment. The study hopes to provide insights into how EMDR can help women cope with the emotional challenges of infertility.

  • Clinical outcomes following prescription of Vosoritide in children with Achondroplasia 0-2 years of age

    An observational study in children 0-2 years of age with ACH who initiate vosoritide treatment, receiving daily subcutaneous injections of vosoritide, followed up in accordance with the Australian achondroplasia management guidelines. Outcomes in treated children will be compared retrospective data of untreated children. A retrospective study (2000-2023) will be undertaken to collect data on children 0-7 years of age who have not had any therapeutic treatment for ACH. It is hypothesised that children receiving vosoritide will have better growth and developmental outcomes compared to historical controls.

  • Resilience and wellbeing in the era of climate change: an acceptability and feasibility pilot of the Bee Well program for treating eco-anxiety in rural children exposed to natural hazards

    This project aims to fill a gap in existing services by helping young people living in rural areas who are feeling distressed about climate change. Specifically, the project aims to support the mental health and resilience of young people aged 10-14 in rural NSW who have been affected by natural disasters such as fire, drought, or flooding. The program will take place outdoors using an interactive workshop. It will draw on the best-available evidence in the field of eco-therapy for mental health resilience in the era of climate change. It is hypothesised that participation in an interactive intervention, designed as a workshop with 5 inter-related modules, will lead to a beneficial change in psychological distress, resilience and emotions related to climate change.

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