ANZCTR search results

This study aims to determine the if telephone support and print materials can increase physical activity participation in lung cancer survivors . Who is it for? You may be eligible to join this study if you have been diagnosed with lung cancer, have no metastatic disease, and are no longer on treatment. Trial details. Participants in this trial will be randomly (by chance) allocated to one of two groups. One group will receive print-based materials and telephone follow-up designed to increase physical activity participation for 12-weeks. The other group will receive print-based materials and telephone follow-up for 12-weeks to ask about their general health and well being. After this time participants in this group will be given print-materials designed to increase physical activity levels. Participants will complete questionnaires about physical activity levels, fatigue and quality of life as well as wear a physical activity monitor at baseline,3 months and six months. It is thought that the intervention will increase physical activity participation when compared to the control.

This study will assess the effect of hyperbaric oxygen therapy on quality of life and saliva in patients with dry mouth (xerostomia) following radiotherapy for head and neck cancer. Who is it for? You may be eligible to join this study if you are aged 18-90 years and have been diagnosed with xerostomia of at least 6 months duration following radiotherapy for head and neck cancer. Trial details Participants in this trial will be randomly (by chance ) allocated to one of two groups. Participants in one group will undergo 30 daily hyperbaric oxygen treatments of 90 minutes duration each. Participants in the other group will receive 30 placebo (control) treatments initially but will be offered the hyperbaric oxygen treatment after 3 months. Participants will not know which group they are in until the trial is completed. Participants will be regularly assessed over a 12 month period to determine their quality of life, saliva components and treatment costs.

This study aims to examine the effect of vibration therapy on markers of bone turnover in prostate cancer survivors on androgen suppression therapy. Who is it for? You may be eligible to join this study if you are a man currently taking an androgen suppression therapy for the treatment of prostate cancer. Trial details. Participants in this trial will be randomly (by chance) allocated to one of two groups. One group will undergo whole body vibration therapy. This involves standing on a gently vibrating platform for 20 minutes, three times per week over a period of 12 weeks. The other group will be assigned to no treatment for the 12 week trial period. After this time participants in this group will be offered the vibration treatment. Participants will give blood and urine samples at baseline and at 12 weeks to examine markers of bone metabolism. They will also complete some tests of physical function and questionnaires about fatigue, quality of life and physical activity levels at these time points. It is thought that vibration training will decrease the breakdown of bone compared to no training.

We propose to see every child, under the age of 16, who has been found in a Clandestine Methamphetamine laboratory, or who is known to have been in this illegal site in the last 7 days. As the Clan Labs are raided we will liaise with WA Police and Department for Child Protection to assess these children. Each child will receive a thorough physical examination, urine toxicology screen, general bloods including liver function test, and a developmental or cognitive assessment. It is our aim to describe the health effects that potentially arise in children exposed to the methamphetamine and toxic chemicals that are used in the illegal manufacture of this drug. We will describe symptoms, abnormal examination findings, developmental and cognitive functioning and report on positive toxicology screens in these children so that we can better understand the health and medical needs of this population, which is unfortunately on the increase as more illegal labs are found around WA. We ultimately plan to devise a protocol for asessment of these children that can be followed Australia wide.

We hypothesise that multimedia patient education technology is superior to the traditional surgeon patient verbal process of obtaining informed consent for a variety of orthopaedic procedures including lateral ligament reconstruction, hallux valgus deformity correction, first metatarsal phalangeal fusion, Morton’s neuroma resection, and ankle arthroscopy.

Young people are faced with numerous and powerful influences to use both licit and illicit drugs, and drug education can play an important counterbalancing role in shaping a normative culture of safety, moderation and informed decision making. The aim of this research is to develop and evaluate the harm reduction effect of a comprehensive, evidence based school drug education program for year eight and nine students in a large, representative sample of Victorian government high schools.

Parents of children who suffer from traumatic brain injury, chronic illnesses and developmental disabilities face a myriad issues that may not be immediately apparent. Apart from the practical responsibilities associated with caring for the ill child, other areas such as making sure that the household continues running smoothly and maintaining finances compete with parents' attentions. In addition to these practical challenges, parents also face internal challenges, such as having to come to terms with the possibility of losing their child, or that their child is not going to live their lives like their peers. Hot on the heels of these realizations are the "whys" and "hows" of their children's conditions, which challenge parents' beliefs about themselves and that of the world that they live in. This especially comes to the fore when parents witness their children suffering and in pain, or compare their children with their normally developing peers. As a result of these various sources of stress, a variety of emotional disorders in parents have been found to result from the diagnosis of their children's disabilities or illnesses. Depression, anxiety, as well as post-traumatic stress symptoms (PTSS) have been found to occur most often, with higher rates commonly found in parents whose children have recently been diagnosed (Vrijmoet-Wiersma et al., 2008). Although the level of emotional distress has been found by researchers to drop as time passes, the impact of distress has been found to have long-reaching consequences, sometimes manifesting as negative family communication, increased family conflict, and negative marital relationships, which then results in a vicious cycle as it feeds back into the emotional distress faced by parents. The diagnosis of illness or disability in a child therefore brings about a great impact on parents and the rest of the family. Although the impact of the diagnoses were described in terms of being external or internal to parents, it must be noted that these challenges interact with each other to produce either positive outcomes of growth or resilience in parents, or negative outcomes of distress. Most of the distress experienced by parents has been found by researchers to be at its most intense at the time of diagnosis, and likely to be maintained in the long run if parents' distress are not addressed. As such, the period following diagnosis appears to be crucial in assisting parents to lower their levels of distress. Hence, a screening tool that correctly identifies distressed parents without taking up too much of their time, as well as an intervention that helps them to reduce their distress, particularly existential distress, is necessary. Study 1 is an evaluative study that aims to evaluate the accuracy of a screening approach that assesses the level of distress of parents of children recently diagnosed with traumatic brain injury, chronic and/or life-threatening illnesses such as cystic fibrosis and cancer, and developmental disabilities. It involves a comparative analysis between a set of six emotion thermometers with a more comprehensive battery of assessment tools that measure depression, anxiety, loss of meaning, and post-traumatic stress disorder (PTSD). The purpose of investigating the utility and accuracy of a screening tool is so that distressed parents can be identified and referred to the various support structures in the hospital. Study 2, on the other hand, aims to compare the treatment outcomes between psychotherapy that is meaning-focused, with cognitive-behavioural treatment (CBT), immediately after treatment and at follow-up three months later. It involves a comparison of the specific components of both forms of therapy which can bring about a reduction of distress in the participants. The order by which the participants will receive both forms of therapy is alternated; that is, participants will be randomly allocated to a group that receives the meaning-focused therapy first, while the other group will receive CBT first, and the order will be switched at the conclusion of the prior treatment. At the conclusion of each treatment, participants will be asked to complete the assessment tools, to find out if there was a reduction in their distress. Hypotheses: 1) There will be a clear indicator of whether the screening tool can identify parents who are distressed. 2) The screening tool will be able to identify parents who may benefit from psychological support. These parents may have been overlooked if the screening tool had not been used. 3) The meaning-focused therapy will reduce parents' distress more than cognitive-behavioural therapy. 4) The greater reduction in distress that is brought about by the meaning-focused therapy than cognitive-behavioural therapy will still be demonstrated by these parents after three months. 5) Parents will report a greater increase in sense of meaning immediately after the meaning-focused component than immediately after the cognitive-behavioural component.

The proposed project will introduce a Nurse Led Intervention (NLI) to engage patients with an admission for cardiovascular disease (CVD) and co-morbid depression and or anxiety. The NLI will facilitate the modification of health related behaviours through motivational interviewing and further education on self care strategies.

This study aims to determine the effect of supervised and home-based exercise training in lung cancer survivors. Who is it for? You may be eligible to join this study if you have been diagnosed with lung cancer and are no longer on treatment. Trial details. Participants in this trial will be randomly (by chance) allocated to one of two groups. One group will undergo supervised and home-based exercise training. This involves resistance (lifting weights) and aerobic exercise (walking), three times per week over a period of 3 months and then will be monitored (without training) for a further 3 months. The other group will be assigned to no treatment for the first 3 months. After this time participants in this group will be given a home-based exercise program and equipment. Participants will complete some tests of physical function and questionnaires about fatigue, and physical activity levels, and have their body composition measured at these time points. It is thought that the exercise program will improve physical function when compared to no training.

This research will investigate the acute effect of whole body vibration (WBV) on sprinting gait and sprint starts in a group of 30 sub-elite sprint athletes that compete in national level athletics championships (18 to 30 yrs). This is a randomised cross-over design with two warm-up treatments and a 7 day wash-out period. There are two stages in this project. In the first stage, participants will be randomly assigned to either a whole body vibration (WBV; n=15) or traditional warm-up modality (TRAD; n=15) for sprinting. Participants will complete the warm-up followed by 6 x 40 m sprints on an athletics track. After a 7 day wash-out period, the participants will repeat the sprint task with the other warm-up modality (cross-over). The following measures will be recorded: 1) reaction time and force production using an instrumented starting block; 2) running pattern using a 2-dimensional motion analysis system; and, 3) 5, 10, 20 and 40 m interval times using timing gates. The randomised cross-over design described above will be used in the second stage of this project to investigate the effect of warm-up modality on over-ground running patterns for steady-state running speeds ranging from 6 to 7 m/s. The patterns will be recorded by a 3-dimensional Vicon Motion Measurement system set up on a netball court in the Bundoora Netball and Sports Centre (BNASC).