7 results on '"Petchler, C."'
Search Results
2. Capturing the value and core concepts of the Clinical Research Nurse
- Author
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Hansen, B.R., Whitehouse, C.L., Nkimbeng, M., Beer, K., Mackintosh, K., Allgood, S., Petchler, C., Wright, R., Hansen, B.R., Whitehouse, C.L., Nkimbeng, M., Beer, K., Mackintosh, K., Allgood, S., Petchler, C., and Wright, R.
- Abstract
Aim To offer a novel, four-point conceptual model that encapsulates the Clinical Research Nurse’s intrinsic value, active leadership, and direct contribution to high quality, person-centered, safe care, addressing current misperceptions of research nursing. Methods This paper describes the provision of ‘care’, safely delivered by the Clinical Research Nurse through a four-point conceptual model and case-driven example. Discussion Clinical research nursing is conceptualized within the domains of Care and Trust, Role, Impact, and Integration. The case example demonstrates real-world application of these domains and the expertise required to balance the complexities of clinical needs and research demands in a healthcare environment. Conclusions This paper offers a mechanism for understanding the importance of the Clinical Research Nurse and their role in maintaining safety and a high-level view of the care arena. These reflections are considered with an international application for the role.
- Published
- 2022
3. 'In our culture, we come when you die': Qualitative descriptive analysis of end-of-life perspectives in a reservation-based community.
- Author
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Nelson KE, Adams K, Kahn-John M, Davidson PM, Ferrell B, Meah M, Petchler C, Ricker A, Runsabove K, Werk A, Wright R, and Brockie TN
- Abstract
Aim: To explore (1) perspectives and attitudes of Native Americans regarding transitions from serious illness to death, and (2) awareness about hospice and palliative care service models in a Great Plains reservation-based community., Design: Qualitative descriptive study., Methods: Community members and clinicians were invited to participate in a semi-structured focus group or interview by Tribal Advisory Board members. Analysis involved three phases: (1) qualitative descriptive analysis of preliminary themes using the Addressing Palliative Care Disparities conceptual model; (2) a cultural review of the data; and (3) reflexive thematic analysis to synthesize findings., Results: Twenty-six participants engaged in two focus groups (n = 5-6 participants in each) and interviews (n = 15). Four themes were derived from their stories: (1) family connectedness is always priority; (2) end-of-life support is a community-wide effort; (3) everyone must grieve in their own way to heal; and (4) support needs from outside the community., Conclusion: Findings highlight cultural considerations spanning the life course. Clinicians, researchers and traditional wisdom keepers and practitioners, particularly those working in rural and/or reservation-based settings, must provide culturally safe care. This must include acknowledging and prioritizing the needs and preferences of Native American patients and the impact on their families and communities., Impact and Implications for the Profession: Leveraging community assets, such as family and social networks, is key for supporting Native American patients with serious illnesses. Additionally, facilitating greater family and caregiver involvement along a patient's care trajectory may be a pathway for easing health care workers' caseloads in reservation-based areas, where resources are limited., Reporting Method: The Consolidated Criteria for Reporting Qualitative Research (COREQ) guideline was used., Patient/public Contribution: The study was ideated based on community insight. Tribal Advisory Board members oversaw all aspects including recruitment, data acquisition, interpretation of findings and tribal data dissemination., (© 2024 John Wiley & Sons Ltd.)
- Published
- 2024
- Full Text
- View/download PDF
4. Integrative review of school integration support following pediatric cancer.
- Author
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Parrillo E, Petchler C, Jacobson LA, Ruble K, Paré-Blagoev EJ, and Nolan MT
- Subjects
- Child, Humans, Qualitative Research, Health Personnel, Communication, Schools, Parents, Cancer Survivors, Neoplasms therapy
- Abstract
Purpose: This study aims to understand parents' experiences of school integration support for their child's transition to K-12 schooling during or after cancer treatment., Methods: This integrative literature review used PubMed, CINAHL, PsycINFO, and Embase databases and included articles from January 2000 to July 2022 describing parent experiences with support from healthcare providers, school faculty/systems, and school integration programs. This review was guided by an adapted School Re-Entry Model and used constant comparison to identify common themes and guide synthesis. The Johns Hopkins Evidence and Quality Guide was used to appraise article quality and level of evidence., Results: Thirty-five articles were included in the final review: seventeen qualitative, fourteen quantitative, and four mixed or multi-method designs. Parents reported experiences receiving support from healthcare providers, school faculty/systems, school integration programs, and "other" sources. Parents reported both facilitators and barriers to communication, knowledge, and the process of receiving school integration support., Conclusions: Parents found neuro/psychologists highly supportive but reported limited support from other healthcare providers. Most parents reported mixed experiences with school faculty and reported many barriers to school system support. Parents reported positive experiences with school integration programs; however, limited programs were available., Implications for Cancer Survivors: Future programs and research should focus on addressing identified barriers and facilitators of school integration support. Further work is also needed to understand a wider range of parent experiences during school integration., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2024
- Full Text
- View/download PDF
5. "They Would Lift My Spirits": Sources of Support for Family Surrogate Decision-Makers at the End of Life.
- Author
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Fisher MC, Parrillo E, Petchler C, Kub J, Hughes MT, Sulmasy DP, Baker D, and Nolan MT
- Subjects
- Humans, United States, Decision Making, Advance Directives, Death
- Abstract
Surrogate decision-makers make critical decisions for loved ones at the end of life, and some experience lasting negative psychological outcomes. Understanding whom they rely on for support and the types of support they value may inform nursing care and that of other health team members who work with surrogates. The purpose of the study was to explore decision support and other types of support provided to surrogate decision-makers at the end of life of their loved one and perceived usefulness of the support. This secondary analysis of data from a mixed-methods study involved the examination of the transcripts of qualitative interviews with 13 surrogate decision-makers in the United States, conducted between 2010 and 2014. A constant comparative method was used to identify common themes surrounding surrogate decision support at the end of life. Surrogates valued advance directives and conversations with their loved one about treatment preferences. Surrogates described involving many different types of people in decision-making and other types of support. Finally, surrogates appreciated being reassured that they were doing a good job in making decisions and seemed to seek out this type of affirmation from various sources including the health care team, family, and friends. Nurses are well-positioned to provide this affirmation because of the time that they spend caring for the patient and family. Future research should further explore the concept of affirmation of surrogates in their role as a means of support as they make decisions for a loved one., Competing Interests: The authors have no conflicts of interest to disclose., (Copyright © 2023 by The Hospice and Palliative Nurses Association. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
6. A qualitative descriptive study of effective leadership and leadership development strategies used by nurse leaders in European island countries.
- Author
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Hughes V, Wright R, Taylor J, Petchler C, and Ling C
- Subjects
- Humans, Qualitative Research, Europe, Ireland, Malta, Leadership
- Abstract
Aim: Nurse leaders influence workplace culture; however, little is known about ethnic cultural influences on nurse leader development. This research aims to identify personal strategies promoting effective leadership by nurse leaders from European small island countries., Design: Descriptive qualitative study., Methods: In 2017, nineteen semi-structured interviews with nurse leaders from England, Greece, Republic of Ireland and Malta explored leadership journeys, strategies employed to support their growth and development, and how cultural identity played a role. Transcripts were analysed using reflexive thematic analysis., Results: Four main themes and 12 subthemes captured the strategies and approaches of the nurse leaders: (1) Influences, (2) Communication, (3) Process and (4) Relationships. These findings reflect and validate the five transformational leadership practices of the Exemplary Leadership Model. While cultural island identity was discussed, there was a shared cultural identity within the role of "nurse leader" that spanned all islands., Patient or Public Contributions: Nineteen nurse leaders contributed to this study., (© 2022 The Authors. Nursing Open published by John Wiley & Sons Ltd.)
- Published
- 2023
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7. Capturing the value and core concepts of the Clinical Research Nurse.
- Author
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Hansen BR, Whitehouse CL, Nkimbeng M, Beer K, Mackintosh K, Allgood S, Petchler C, and Wright R
- Abstract
Background: As nurses, we identify our profession as a caring one, but how does this identity translate from a conceptual definition, to real-world practice for the Clinical Research Nurse?, Aim: To offer a novel, four-point conceptual model that encapsulates the Clinical Research Nurse's intrinsic value, active leadership, and direct contribution to high quality, person-centered, safe care, addressing current misperceptions of research nursing., Methods: This paper describes the provision of 'care', safely delivered by the Clinical Research Nurse through a four-point conceptual model and case-driven example., Discussion: Clinical research nursing is conceptualized within the domains of Care and Trust, Role, Impact, and Integration. The case example demonstrates real-world application of these domains and the expertise required to balance the complexities of clinical needs and research demands in a healthcare environment., Conclusions: This paper offers a mechanism for understanding the importance of the Clinical Research Nurse and their role in maintaining safety and a high-level view of the care arena. These reflections are considered with an international application for the role., Competing Interests: Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article., (© The Author(s) 2022.)
- Published
- 2022
- Full Text
- View/download PDF
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