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    <title>Epworth Collection:</title>
    <link>http://hdl.handle.net/11434/444</link>
    <description />
    <pubDate>Sun, 21 Jun 2026 13:08:52 GMT</pubDate>
    <dc:date>2026-06-21T13:08:52Z</dc:date>
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      <title>Efficacy and cost-effectiveness of an online mindfulness program (MindOnLine) to reduce fear of recurrence among people with cancer: study protocol for a randomised controlled trial</title>
      <link>http://hdl.handle.net/11434/2401</link>
      <description>Title: Efficacy and cost-effectiveness of an online mindfulness program (MindOnLine) to reduce fear of recurrence among people with cancer: study protocol for a randomised controlled trial
Epworth Authors: Wootten, Addie; Gillan, Kate
Abstract: Introduction: Fear of cancer recurrence (FCR) is a common condition among cancer survivors that can lead to significant levels of distress, anxiety and depression. Online mindfulness programmes may provide the mechanism to support cancer survivors manage FCR and distress, and improve people’s well-being over the short, medium and long term. The primary aim of this study is to determine the potential efficacy of MindOnLine, a 9 session mindfulness-based programme for survivors of breast, prostate and colorectal cancer. A formal economic programme will also be conducted.&#xD;
&#xD;
Methods and analysis: A single-blind randomised controlled trial to determine the efficacy and cost-efficacy of a MindOnLine programme for cancer survivors. A total of 400 people living with cancer will be recruited via online advertisements on social media platforms, peak consumer advocacy groups or through outpatient services at healthcare providers across Victoria, Australia. People will be randomly allocated to either the MindOnLine programme (n=200) or waitlist control (n=200). Participant assessments will occur at baseline, at 9 weeks and 9-month follow-up. The primary outcome is change in Fear of Recurrence Index Score total score between baseline and 9 weeks; secondary outcomes are changes in depression and anxiety, quality of life and mindfulness. The economic analysis comprises a cost-consequences analysis where all outcomes will be compared with costs.&#xD;
&#xD;
Ethics and dissemination: Ethics approval was obtained from the Peter MacCallum Cancer Centre (20-53) and Deakin University (2020-284). All participants will be required to provide written informed consent. Findings will be disseminated in peer reviewed journals and among key stakeholder organisations including hospitals, cancer and community organisations and Government. If successful the project will be rolled out nationally with a formal implementation plan.</description>
      <pubDate>Sat, 01 Jan 2022 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11434/2401</guid>
      <dc:date>2022-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Coenzyme Q(10)--its role as a prooxidant in the formation of superoxide anion/hydrogen peroxide and the regulation of the metabolome.</title>
      <link>http://hdl.handle.net/11434/2395</link>
      <description>Title: Coenzyme Q(10)--its role as a prooxidant in the formation of superoxide anion/hydrogen peroxide and the regulation of the metabolome.
Epworth Authors: Linnane, A. W.
Abstract: Coenzyme Q10 plays a central role in cellular bioenergy generation and its regulation. Closed membrane systems generate a proton motive force to create transient localized bio-capacitors; the captured energy is used for the synthesis of mitochondrial ATP but also for many other processes, such as metabolite translocations, nerve conduction and a host of other bioenergy requiring processes. Coenzyme Q10 plays a key role in many of these sub-cellular membrane energy generating systems. Integral to this phenomenon is the prooxidant role of coenzyme Q10 in generating the major superoxide anion/hydrogen peroxide second messenger system. This messenger system, largely but not exclusively, arises from coenzyme Q10 semiquinone function; it contributes to the regulation of sub-cellular redox potential levels; transcription/gene expression control; is essential for modulated protein turnover and activation; mediates hormone and growth factor extracellular signaling. The regulated prooxidant formation of the superoxide anion/H2O2 second messenger system is essential for the normal physiological function of the metabolome. The normally functioning metabolome is the expression of a finely tuned dynamic equilibrium comprised of thousands of anabolic and catabolic reactions and all cellular signaling systems must be finely regulated. There is still much to be learned about the up/down regulation of the H2O2 messenger system.  The concept that superoxide anion/H2O2 cause random macromolecular damage is rebutted. The administration of antioxidants to quench the inferred toxicity of these compounds as a therapy for age associated diseases is unsupported by extant mammalian clinical trials and should be subject to serious re-evaluation. The role of ascorbic acid as a beneficial hydrogen peroxide prodrug is discussed.</description>
      <pubDate>Thu, 01 Mar 2007 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11434/2395</guid>
      <dc:date>2007-03-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>The age-associated decrease in the amount of amplifiable full-length mitochondrial DNA in human skeletal muscle.</title>
      <link>http://hdl.handle.net/11434/2008</link>
      <description>Title: The age-associated decrease in the amount of amplifiable full-length mitochondrial DNA in human skeletal muscle.
Epworth Authors: Kovalenko, Sergey
Abstract: A variety of techniques have been applied to investigate the interrelationship between age-related atrophy of rat soleus muscle and other signs of muscle aging, such as changes in muscle fibre type composition, decrease in bioenergy capacity and accumulation of mitochondrial DNA (mtDNA) arrangements. Age-related atrophy of rat soleus muscle was shown to start at the age of about 28 months. It was accompanied by a decrease in the number of slow twitch muscle fibres (type I) and an increase in the proportion of muscle fibres co-expressing slow and fast myosins (type Ic and IIc fibres). Bioenergy capacity of the soleus muscle, assessed by the level of measurable cytochrome c oxidase (COX) activity, was found to be decreased both in the middle age and old rats compared to the young animals. Muscle atrophy was also accompanied by a decrease in the amount of full-lengthmitochondrial DNA (FL-mtDNA) amplifiable by the extra-long PCR (XL-PCR) and the increase in the number of mtDNA deletions. The results of the study show that the decline in the bioenergy capacity of the rat soleus occurs by the middle age. It is followed by the onset of the age-related muscle atrophy that is accompanied by both fibre type changes and functional mtDNA degradation.</description>
      <pubDate>Tue, 01 Jan 2002 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11434/2008</guid>
      <dc:date>2002-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Relative risks and odds ratios: simple rules on when and how to use them.</title>
      <link>http://hdl.handle.net/11434/1864</link>
      <description>Title: Relative risks and odds ratios: simple rules on when and how to use them.
Epworth Authors: McKenzie, Dean; Thomas, Christopher
Abstract: AIM:&#xD;
Relative risks and odds ratios are widely reported in the medical literature, but the latter can be very difficult to understand. We sought to further clarify these important indices.&#xD;
&#xD;
METHODS:&#xD;
We defined both relative risks and odds ratios, then looked at the types of study for which each statistic is suited. We illustrated calculation of relative risks and odds ratios through analysis of tabled data from a recent published longitudinal study, using a 2x2 table, bar charts and R, the open source statistical programming language. Simple rules for when and how to use relative risks and odds ratios are presented.&#xD;
&#xD;
CONCLUSION:&#xD;
Understanding the difference between relative risks and odds ratios and when and how to use them may aid clinical interpretation, dissemination and translation of research findings.</description>
      <pubDate>Wed, 01 Apr 2020 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11434/1864</guid>
      <dc:date>2020-04-01T00:00:00Z</dc:date>
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