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  <title>DSpace Collection:</title>
  <link rel="alternate" href="https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/20" />
  <subtitle />
  <id>https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/20</id>
  <updated>2026-06-14T02:06:53Z</updated>
  <dc:date>2026-06-14T02:06:53Z</dc:date>
  <entry>
    <title>The experience of registered nurses who mentor undergraduate nursing students in the Australian rural context</title>
    <link rel="alternate" href="https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/758" />
    <author>
      <name>Bowen, L.J.</name>
    </author>
    <id>https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/758</id>
    <updated>2026-06-09T04:12:32Z</updated>
    <published>2014-01-01T00:00:00Z</published>
    <summary type="text">Title: The experience of registered nurses who mentor undergraduate nursing students in the Australian rural context
Authors: Bowen, L.J.
Abstract: On rural clinical placements, undergraduate nursing students work alongside registered nurses sharing their patient allocation. The registered nurse facilitates the student’s clinical learning, providing opportunities for the student to translate theoretical knowledge into clinical practice. Despite the challenges of the rural context, registered nurses partner with universities to support and mentor students. This study explored the experience of registered nurses who mentored undergraduate nursing students on clinical placement in a rural context. It identified communication and information exchange with universities as a frustrating aspect of the mentoring experience, which being amenable to change, was addressed with an intervention.
Description: Hard copy available to borrow from the library.</summary>
    <dc:date>2014-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Improvement in clinicians' perceptions of inpatient urinary continence care following an implementation study: a before and after study using a questionnaire aligned to the Theoretical Domains Framework with practical methods for analysing and presenting barrier and enabler data</title>
    <link rel="alternate" href="https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/685" />
    <author>
      <name>Marsden, D. L.</name>
    </author>
    <author>
      <name>Boyle, K.</name>
    </author>
    <author>
      <name>Birnie, J.</name>
    </author>
    <author>
      <name>Buzio, A.</name>
    </author>
    <author>
      <name>Dunne, J.</name>
    </author>
    <author>
      <name>Hill, K.</name>
    </author>
    <author>
      <name>Lambkin, D.</name>
    </author>
    <author>
      <name>Lever, S.</name>
    </author>
    <author>
      <name>Minett, F.</name>
    </author>
    <author>
      <name>Ormond, S.</name>
    </author>
    <author>
      <name>Shipp, J.</name>
    </author>
    <author>
      <name>Steel, J.</name>
    </author>
    <author>
      <name>Styles, A.</name>
    </author>
    <author>
      <name>Wiggers, J.</name>
    </author>
    <author>
      <name>Cadilhac, D. A-M.</name>
    </author>
    <author>
      <name>Duff, J.</name>
    </author>
    <author>
      <name>I-SCAMP Project Team</name>
    </author>
    <id>https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/685</id>
    <updated>2025-12-17T04:14:40Z</updated>
    <published>2025-10-14T00:00:00Z</published>
    <summary type="text">Title: Improvement in clinicians' perceptions of inpatient urinary continence care following an implementation study: a before and after study using a questionnaire aligned to the Theoretical Domains Framework with practical methods for analysing and presenting barrier and enabler data
Authors: Marsden, D. L.; Boyle, K.; Birnie, J.; Buzio, A.; Dunne, J.; Hill, K.; Lambkin, D.; Lever, S.; Minett, F.; Ormond, S.; Shipp, J.; Steel, J.; Styles, A.; Wiggers, J.; Cadilhac, D. A-M.; Duff, J.; I-SCAMP Project Team
Abstract: Background: Although 10-50% of patients in hospital experience urinary continence issues many do not receive guideline-recommended care. We developed and tested a co-created practice-change package that improved then maintained the proportion of symptomatic inpatients receiving a urinary continence assessment, diagnosis, and management plan. In this present study we aimed to categorise clinicians' perceptions of urinary continence care as barriers or enablers, and determine any change after implementation of the package.&#xD;
&#xD;
Methods: Overall, fifteen adult wards (acute = 3, rehabilitation = 7, acute and rehabilitation = 5) in 12 Australian hospitals (large city = 4, regional = 8) participated. All wards were to receive the practice-change package during the study. The selected implementation strategies addressed barriers identified before implementation, and targeted inpatient clinicians. These clinicians were invited to complete a web-based questionnaire before and immediately after the 6-month implementation phase. The questionnaire was aligned to 13/14 domains of the Theoretical Domains Framework. It included 57 subitems covering assessment, diagnosis, management, or general continence care. A 5-point Likert scale was used (e.g. "strongly agree" to "strongly disagree"). To categorise responses, each subitem was dichotomised as positive (e.g. "agree", "strongly agree") or neutral/ negative ("unsure", "disagree", "strongly disagree"). Subitems were classified and colour coded as barriers (&lt; 60% positive responses, red), neutral (60-69% positive, orange) or enablers (&gt; 69% positive, green). Changes from before to after-implementation were assessed.&#xD;
&#xD;
Results: Clinicians from 12 hospitals participated before-implementation (n=291, 82% female, 88% nursing), and from 10/12 hospitals (n=195, 86% female, 94% nursing) after-implementation. Two hospitals withdrew as the start of their implementation phase coincided with the onset of COVID-19. After implementation substantial improvements in perceptions were observed in 7/13 TDF domains: "skills", "knowledge", "memory", "beliefs about capabilities", "emotion", "environmental context and resources", and "social and professional role". Three domains ("goals", "beliefs about consequences" and "reinforcement") were high scoring enablers at both timepoints. Three domains had limited or no change ("social influences", "intentions", "behaviour regulation").&#xD;
&#xD;
Conclusion: Categorisation and colour-coding of perceptions can assist end-users to quickly understand the data, identify areas for improvement, and changes after-implementation. The results helped to identify and explain which implementation strategies appeared to be successful in changing practice, and which ones need refining.</summary>
    <dc:date>2025-10-14T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Palliative Care for People With Very Severe to Extreme Behavioural and Psychological Symptoms of Dementia (BPSD): A Scoping Review</title>
    <link rel="alternate" href="https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/657" />
    <author>
      <name>Gallop, M.</name>
    </author>
    <author>
      <name>Ford, J.</name>
    </author>
    <author>
      <name>Bowman, A.</name>
    </author>
    <author>
      <name>Mullen, A.</name>
    </author>
    <author>
      <name>Schwebel, D.</name>
    </author>
    <author>
      <name>Johnson, A.</name>
    </author>
    <author>
      <name>Fernandez, R.</name>
    </author>
    <id>https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/657</id>
    <updated>2025-06-27T04:30:51Z</updated>
    <published>2025-05-01T00:00:00Z</published>
    <summary type="text">Title: Palliative Care for People With Very Severe to Extreme Behavioural and Psychological Symptoms of Dementia (BPSD): A Scoping Review
Authors: Gallop, M.; Ford, J.; Bowman, A.; Mullen, A.; Schwebel, D.; Johnson, A.; Fernandez, R.
Abstract: Aim: To explore current evidence regarding the provision of palliative care for individuals with very severe to extreme behavioural and psychological symptoms of dementia (BPSD) in a hospital setting.&#xD;
&#xD;
Design: Scoping review.&#xD;
&#xD;
Reporting method: The PRISMA-ScR reporting guideline.&#xD;
&#xD;
Methods: The JBI guidelines for scoping reviews were followed. A data extraction form assisted in the identification of key findings via a process of content analysis.&#xD;
&#xD;
Data sources: Studies were obtained from bibliographic databases of PubMed, CINAHL, and PsycINFO.&#xD;
&#xD;
Results: This review included six articles, and nine categories emerged from the findings. Symptom assessment and management, pain assessment challenges, atypical presentation of end-stage dementia, complex prescribing and treatment practices, principles of person-centred care, collaboration; training for health care professionals; emotional impact on staff; and family and caregivers.&#xD;
&#xD;
Conclusions: This scoping review highlighted a significant gap in the literature regarding palliative care for people living with very severe to extreme BPSD in hospital settings. This review highlighted key differences in the presentation of people with BPSD needing palliative care. There is a need for tailored models of care, specialised training and education for health professionals, families, and carers, and recognition of dementia as a terminal illness.&#xD;
&#xD;
Implications for the profession and/or patient care: The results of this review provide valuable insights into the level of understanding about the unique palliative care needs for people experiencing very severe to extreme BPSD, making an important contribution to the planning and development of future models of care.&#xD;
&#xD;
Impact: Mapping the available literature highlights a paucity of research in palliative care for people with very severe to extreme BPSD in hospital settings. There is a need for rigorous research studies and models of care developed and informed by the evidence for this small population necessitating unique care needs.</summary>
    <dc:date>2025-05-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Learning to be a midwife in the clinical environment; tasks, clinical practicum hours or midwifery relationships</title>
    <link rel="alternate" href="https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/599" />
    <author>
      <name>Ebert, L.</name>
    </author>
    <author>
      <name>Tierney, O.</name>
    </author>
    <author>
      <name>Jones, D.</name>
    </author>
    <id>https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/599</id>
    <updated>2025-03-27T23:55:57Z</updated>
    <published>2016-01-01T00:00:00Z</published>
    <summary type="text">Title: Learning to be a midwife in the clinical environment; tasks, clinical practicum hours or midwifery relationships
Authors: Ebert, L.; Tierney, O.; Jones, D.
Abstract: Discussions continue within the midwifery profession around the number of and type of clinical experiences required to ensure competent midwifery graduates. Introduction of the three year Bachelor of Midwifery in Australia, almost two decades ago, was intended to reduce the pressure students were under to complete their academic requirements whilst ensuring students developed midwifery practice that encapsulates the philosophical values of midwifery. Currently, midwifery students are mandated to achieve a minimum number of clinical skills and Continuity of Care Experience (CCE) relationships in order to register upon completion of their degree. To achieve these experiences, universities require students to complete a number of clinical practicum hours. Furthermore students are required to demonstrate competent clinical performance of a number of clinical skills. However, there is no evidence to date that a set number of experiences or hours ensures professional competence in the clinical environment. The aim of this paper is to promote discussion regarding the mandated requirements for allocated clinical practicum hours, specified numbers of clinical-based skills and CCE relationships in the context of learning to be a midwife in Australia.&#xD;
&#xD;
Keywords: Clinical education; Competency; Continuity of Care Experience; Midwifery; Midwifery relationships; Work Integrated Learning.</summary>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </entry>
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