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  <channel rdf:about="http://hdl.handle.net/10453/148711">
    <title>OPUS Collection:</title>
    <link>http://hdl.handle.net/10453/148711</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://hdl.handle.net/10453/154582" />
        <rdf:li rdf:resource="http://hdl.handle.net/10453/152270" />
        <rdf:li rdf:resource="http://hdl.handle.net/10453/151234" />
        <rdf:li rdf:resource="http://hdl.handle.net/10453/146625" />
      </rdf:Seq>
    </items>
    <dc:date>2026-04-14T11:04:47Z</dc:date>
  </channel>
  <item rdf:about="http://hdl.handle.net/10453/154582">
    <title>Designing Supportive e-Interventions for Partners of Men With Prostate Cancer Using Female Partners’Experiences: Qualitative Exploration Study</title>
    <link>http://hdl.handle.net/10453/154582</link>
    <description>Title: Designing Supportive e-Interventions for Partners of Men With Prostate Cancer Using Female Partners’Experiences: Qualitative Exploration Study
Authors: Winter, N; Green, A; Jongebloed, H; Ralph, N; Chambers, S; Livingston, P
Abstract: &lt;jats:sec&gt;
            &lt;jats:title&gt;Background&lt;/jats:title&gt;
            &lt;jats:p&gt;Partners of men living with prostate cancer (PCa) can experience a variety of unmet needs that are largely unaddressed by health care professionals. There is limited evidence to suggest which approach may be most effective in supporting partners’ unmet needs and further research is required to determine how to provide support to caregivers and how technology solutions can be designed.&lt;/jats:p&gt;
          &lt;/jats:sec&gt;
          &lt;jats:sec&gt;
            &lt;jats:title&gt;Objective&lt;/jats:title&gt;
            &lt;jats:p&gt;This study aims to explore the experience of partners of men living with PCa and their perceptions of the potential role of information technology in supporting their needs.&lt;/jats:p&gt;
          &lt;/jats:sec&gt;
          &lt;jats:sec&gt;
            &lt;jats:title&gt;Methods&lt;/jats:title&gt;
            &lt;jats:p&gt;A qualitative descriptive methodology using focus groups and phone interviews was used. Purposive sampling was used to recruit people attending a national conference supported by a national PCa organization. Interview guides were adapted from an existing evidence-based smartphone app for caregivers of people with colorectal cancer. Sessions were audio recorded and transcribed verbatim. A coding framework was developed, and transcripts were coded line by line into the framework. Codes within the framework were grouped into descriptive categories that were then developed into analytical themes.&lt;/jats:p&gt;
          &lt;/jats:sec&gt;
          &lt;jats:sec&gt;
            &lt;jats:title&gt;Results&lt;/jats:title&gt;
            &lt;jats:p&gt;A total of 17 female partners participated in the study, with an average age of 64 (SD 8.5) years. The following two main themes emerged: In the first theme, that is, How technology can be shaped to support female partners of prostate cancer survivors, the content and design of the smartphone app was discussed in addressing female partners’ needs. The following four subthemes were developed: getting support from social networks and resources, the lack of relevant information, demystifying future care expectations during and following a PCa diagnosis, and delivering the smartphone app—to whom and from whom. In the second theme, that is, The benefits and barriers of technology, the suitability of smartphone apps as a supportive modality for female partners was described. This included three subthemes: the smartphone app as an appropriate modality for supporting female partners, the future anticipated benefits of using the smartphone app, and concerns for storing and accessing information on the internet.&lt;/jats:p&gt;
          &lt;/jats:sec&gt;
          &lt;jats:sec&gt;
            &lt;jats:title&gt;Conclusions&lt;/jats:title&gt;
            &lt;jats:p&gt;A smartphone app may be a suitable modality for providing information and peer support to female partners of men living with PCa. There is a need to provide peer support for female partners in future interventions to ensure that female partners’ intimacy and daily practical needs are met.&lt;/jats:p&gt;
          &lt;/jats:sec&gt;</description>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10453/152270">
    <title>Prostate cancer survivorship essentials framework: guidelines for practitioners.</title>
    <link>http://hdl.handle.net/10453/152270</link>
    <description>Title: Prostate cancer survivorship essentials framework: guidelines for practitioners.
Authors: Dunn, J; Green, A; Ralph, N; Newton, RU; Kneebone, A; Frydenberg, M; Chambers, SK
Abstract: OBJECTIVE:To develop contemporary and inclusive prostate cancer survivorship guidelines for the Australian setting. PARTICIPANTS AND METHODS:A four-round iterative policy Delphi was used, with a 47-member expert panel that included leaders from key Australian and New Zealand clinical and community groups and consumers from diverse backgrounds, including LGBTQIA people and those from regional, rural and urban settings. The first three rounds were undertaken using an online survey (94-96% response) followed by a fourth final face-to-face panel meeting. Descriptors for men's current prostate cancer survivorship experience were generated, along with survivorship elements that were assessed for importance and feasibility. From these, survivorship domains were generated for consideration. RESULTS:Six key descriptors for men's current prostate cancer survivorship experience that emerged were: dealing with side effects; challenging; medically focused; uncoordinated; unmet needs; and anxious. In all, 26 survivorship elements were identified within six domains: health promotion and advocacy; shared management; vigilance; personal agency; care coordination; and evidence-based survivorship interventions. Consensus was high for all domains as being essential. All elements were rated high on importance but consensus was mixed for feasibility. Seven priorities were derived for immediate action. CONCLUSION:The policy Delphi allowed a uniquely inclusive expert clinical and community group to develop prostate cancer survivorship domains that extend beyond traditional healthcare parameters. These domains provide guidance for policymakers, clinicians, community and consumers on what is essential for step change in prostate cancer survivorship outcomes.</description>
    <dc:date>2021-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10453/151234">
    <title>Experiences of female partners of prostate cancer survivors: A systematic review and thematic synthesis</title>
    <link>http://hdl.handle.net/10453/151234</link>
    <description>Title: Experiences of female partners of prostate cancer survivors: A systematic review and thematic synthesis
Authors: Green, A; Winter, N; DiGiacomo, M; Oliffe, JL; Ralph, N; Dunn, J; Chambers, SK</description>
    <dc:date>2021-10-27T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10453/146625">
    <title>A Multicomponent Nonpharmacological Intervention to Prevent Delirium for Hospitalized People with Advanced Cancer: A Phase II Cluster Randomized Waitlist Controlled Trial (The PRESERVE Pilot Study).</title>
    <link>http://hdl.handle.net/10453/146625</link>
    <description>Title: A Multicomponent Nonpharmacological Intervention to Prevent Delirium for Hospitalized People with Advanced Cancer: A Phase II Cluster Randomized Waitlist Controlled Trial (The PRESERVE Pilot Study).
Authors: Hosie, A; Phillips, J; Lam, L; Kochovska, S; Noble, B; Brassil, M; Kurrle, S; Cumming, A; Caplan, GA; Chye, R; Ely, EW; Lawlor, PG; Bush, SH; Davis, JM; Lovell, M; Parr, C; Williams, S; Hauser, K; McArdle, S; Jacquier, K; Phillipson, C; Kuwahata, L; Kerfoot, J; Brown, L; Fazekas, B; Cheah, SL; Edwards, L; Green, A; Hunt, J; Attwood, R; Assen, T; Garcia, M; Wilcock, J; Agar, M
Abstract: Background: Delirium is a common debilitating complication of advanced cancer. Objective: To determine if a multicomponent nonpharmacological delirium prevention intervention was feasible for adult patients with advanced cancer, before a phase III (efficacy) trial. Design: Phase II (feasibility) cluster randomized controlled trial. All sites implemented delirium screening and diagnostic assessment. Strategies within sleep, vision and hearing, hydration, orientation, mobility, and family domains were delivered to enrolled patients at intervention site admission days 1-7. Control sites then implemented the intervention ("waitlist sites"). Setting: Four Australian palliative care units. Measurements: The primary outcome was adherence, with an a priori endpoint of at least 60% patients achieving full adherence. Secondary outcomes were interdisciplinary care delivery, delirium measures, and adverse events, analyzed descriptively and inferentially. Results: Sixty-five enrolled patients (25 control, 20 intervention, and 20 waitlist) had 98% delirium screens and 75% diagnostic assessments completed. Nurses (67%), physicians (16%), allied health (8.4%), family (7%), patients (1%), and volunteers (0.5%) delivered the intervention. There was full adherence for 5% patients at intervention sites, partial for 25%. Both full and partial adherence were higher at waitlist sites: 25% and 45%, respectively. One-third of control site patients (32%) became delirious within seven days of admission compared to one-fifth (20%) at both intervention and waitlist sites (p = 0.5). Mean (standard deviation) Delirium Rating Scale-Revised-1998 scores were 16.8 + 12.0 control sites versus 18.4 + 8.2 (p = 0.6) intervention and 18.7 + 7.8 (p = 0.5) waitlist sites. The intervention caused no adverse events. Conclusion: The intervention requires modification for optimal adherence in a phase III trial.</description>
    <dc:date>2020-10-01T00:00:00Z</dc:date>
  </item>
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