Auflistung nach Autor:in "Liebig, Brigitte"
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Publikation Aktive Vaterschaft als Karriere-Turbo für arbeitende Mütter?(HR today Verlag, 2015) Kron, Christian; Liebig, Brigitte01B - Beitrag in Magazin oder ZeitungPublikation Anrecht auf Vereinbarung? Vereinbarkeitsansprüche von Vätern in Schweizer Arbeitsorganisationen(Seismo, 2021) Peitz, Martina; Liebig, BrigitteWandel und Persistenz der Geschlechterverhältnisse in Arbeitswelt, Familie und Politik bedeuten für Männer* und Männlichkeit(en) spezifische Möglichkeiten und Herausforderungen. Zur Debatte steht, was sich gegenwärtig überhaupt verändert. Welche Entwicklungen werden ausgemacht? Welche Potenziale, Widersprüche und Spannungen – für Männer* und für die Gesellschaft – tun sich auf oder entstehen dadurch? Wie haben sich Männlichkeiten historisch in der Schweiz überhaupt gestaltet und ausgebildet? Das Buch bündelt Forschungsbeiträge zu Männlichkeit(en) in der Schweiz, die zu einer kritischen Zeitdiagnose beitragen. Dabei werden Perspektiven aus verschiedenen Disziplinen – der Geschlechterforschung, Soziologie, Sozialen Arbeit, Geschichte, Literaturwissenschaft, Psychologie und Migrationsforschung – eingebracht.04A - Beitrag SammelbandPublikation Betriebliche Politik der Emotionen. Zur Organisation der Gefühle am Arbeitsplatz(Carl-Auer Verlag, 2014) Liebig, Brigitte; Geramanis, Olaf; Hermann, Kristina04A - Beitrag SammelbandPublikation Betriebliche Sozialarbeit — wer engagiert sich und aus welchen Gründen?(Haupt, 2010) Baumgartner, Edgar; Liebig, Brigitte04A - Beitrag SammelbandPublikation Care Coordination in Palliative Home Care: Who Plays the Key Role?(Ubiquity Press, 2020) Reeves, Emily; Liebig, Brigitte; Schweighoffer, RekaBackground: Clearly identified professionals who are appointed for care coordination are invaluable for ensuring efficient coordination of health care services. However, challenges to identifying roles in palliative care are well documented in literature. Notably, in order to meet high demands on palliative home care settings, many care practitioners perform tasks that surpass the responsibilities and regulations of their role, including care coordination. Without clearly defined roles, standards of care cannot be guaranteed. Yet, little is understood about who plays the key role in palliative home care. Aim: The present study aims to address the gap in the research by identifying who plays a key role in coordination in palliative home care. Methods: Interviews with general practitioners (GPs), nurses and relatives of palliative patients were carried out in Swiss cantons (Vaud, Ticino, Luzern and Basel) to identify key coordinators of care. Interviews were analyzed using content analysis and presented using grounded theory. Results: Findings indicated that there was considerable ambiguity of the key coordinator role. 1) Causal conditions of this phenomenon were; informality of professional roles and lack of communication between team members, 2) Consequences of this included; conflicting understandings of key coordinator role and family members feeling overburdened, 3) Strategies adopted by interviewees included; adapting or taking control of care coordination. These findings are highly indicative of areas for improvement for care coordination in palliative home care settings. Specifically, they underline a profound need for clear communication between palliative care service providers regarding which professionals assume a key coordative role, or who are delegated a coordinative role at any given time. Crucially, since the findings reveal that relatives are intimately involved in care coordination, the findings point to a lack of adequate financial and psycho-social support for relatives of palliative patients who are burdened with coordination tasks, without the appropriate recompense.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Collaboration in Palliative Care Networks in Urban and Rural Regions of Switzerland(01/2019) Schweighoffer, Reka; Nagy, Noemi; Reeves, Emily; Liebig, BrigitteDue to aging populations, the need for seamless palliative care provision is of central interest for western societies. An essential aspect of palliative care delivery is the quality of collaboration amongst palliative care providers. Therefore, thecurrent research is based on Bainbridge’s conceptual framework,which provides an outline for the evaluation of palliative careprovision. This study is the first one to investigate the predictive validity of spatial distribution on the quantity of interaction amongst various palliative care providers. Furthermore, based on the familiarity principle, we examine whether the extent of collaboration influences the perceived quality of collaboration among palliative care providers in urban versus rural areas of Switzerland. Based on a population-representative survey of Swiss palliative care providers, the results of the current study show that professionals in densely populated areas report higher absolute numbers of interactions and are more satisfied with their collaborative practice. This indicates that palliative care providers who work in urban areas are better embedded into networks than their counterparts in more rural areas. The findings are especially important, considering that efficient collaboration is a prerequisite to achieve satisfactory patientoutcomes. Conclusively, measures should be taken to foster collaboration in weakly interconnected palliative care networks.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Collaborative Networks in Primary and Specialized Palliative Care in Switzerland - Perspectives of Doctors and Nurses(Bentham, 2020) Schweighoffer, Reka; Reeves, Emily; Liebig, BrigitteTo date, information about collaborative networks of doctors and nurses in palliative care is still scarce, yet of great importance in revealing gaps in collaboration. This paper investigates the collaboration frequencies of medical doctors and nurses within, and across, different settings of palliative care. The study was based on a Swiss national survey on “Collaboration and cooperation in Palliative Care”. The subjects surveyed included service providers in the primary and specialized palliative care sectors, as well as support services (N=1111). Information about ties between providers was gathered by asking professionals to estimate the frequency of interaction with other professionals within the last year, on a daily, weekly, monthly and yearly basis. Social network analysis was used to assess the interaction patterns of nurses and doctors (N= 728) in primary and specialized care settings. Visual representations indicated that, contrary to primary care settings, healthcare providers in specialized care settings reported of numerous interactions with other professions. In primary care, general practitioners reported the least frequent interactions with other professions. Of all providers investigated, specialized doctors in hospitals and hospices reported the densest collaborative networks. Gaps regarding collaboration in Swiss palliative care provision were revealed. Based on the results of the study, recommendations on how to improve service quality by strengthening the interaction patterns of general practitioners, as well as community-based palliative care, are provided.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Community readiness for Palliative Care Services in Switzerland: Basis for public health strategy for health psychologists(Psychreg, 04/2019) Reeves, Emily; Schweighoffer, Reka; Liebig, BrigitteIntegrated healthcare delivery is essential for ensuring health cost efficiency and high quality care for patients. In Switzerland, cantonal differences in approaches to palliative careimplementation contribute to fragmented provision of palliative care services. ‘Community readiness’is a practical tool for assessing the status and change in community health services. The aim of this paper is to assess community readiness for palliative care services in Switzerland. A document analysis was carried out in combination with expert interviews with palliative caremembers in four Swiss cantons (Ticino, Vaud, Basel-City and Lucerne). The findings indicate differences with respect to the history, provisional structure, coordination and financial support for palliative care in the cantons. Findings indicate that future research to improve provisional structures, financing and educational opportunities for PC in the cantons, specific to the needs of the canton, warrant investigation01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Comparing the Perspectives of Professionals and Relatives Toward the Quality of Palliative Care: A Qualitative Study(LIDSEN, 2020) Reeves, Emily; Liebig, Brigitte; Degen, EvelineHigh-quality care is an important aim of palliative care services. However, the quality of care is a complex phenomenon and is subjectively perceived by those who are closest to the services and are often evaluated poorly. Prior research has highlighted the difficulties in evaluating the quality of care because of different perspectives, and still, only a little is understood about the perception of the quality of care in palliative care services. Investigating the perspectives of key individuals involved in palliative care, such as palliative professionals and relatives of palliative patients, can provide invaluable insight to understand the quality of care. To identify the perceptions of palliative professionals and relatives of the patients toward the quality of palliative care along with identifying the similarities and divergences in the perceptions, as well as highlighting the complexity of quality in palliative care settings while indicating their areas of improvement. This was a qualitative study that involved semi-structured interviews for the evaluation of palliative care guided by the proposed system approach model [1]. The interviews were conducted with a total number of 38 professionals working in palliative care along with 26 relatives of palliative patients across four Swiss cantons (Ticino, Basel, Vaud, and Lucerne). These professionals worked in primary palliative care (PPC) and specialized palliative care (SPC), where 11 general practitioners (GP’s) and 12 nurses were from primary palliative care services. Additionally, 15 interviews were conducted with 9 specialized medical doctors (e.g., oncologists) and 6 specialized palliative care nurses from different hospitals, hospices, mobile palliative care teams (MPCT’s), and specialist private practice. The results revealed considerable differences between the perspectives of professionals and relatives regarding the following aspects of care: 1) the availability, 2) client-centeredness (including respect for patient’s wishes and relative’s involvement in care, 3) satisfaction (including physical and psychosocial), and 4) communication and information transfer. Mainly, the family members felt that care was not being always readily available and coordinated poorly, the patient’s needs were overlooked because of the lack of time. Also, some professionals were perceived to be incompetent with a lack of communication and negligence toward the psychosocial needs of the patient. On the other hand, professionals indicated that relatives may be too involved in the patient care and might have expressed concern due to the high risk of burn out caused by extreme stress and emotionally taxing circumstances of palliative care. The different perspectives uncovered both the similarities and discrepancies, representing a demand for addressing the shortcomings of palliative care services. Specifically, findings indicated that professionals may overestimate the quality of palliative care. Also, future initiatives were needed to ensure that the family members of palliative patients were adequately supported, both psycho-socially and financially, justifying the investment. These findings would help in informing the health policy about the aspects of care that require specific attention to improve the overall quality of care and urge future research to explore the best ways to support these aspects of care.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Conciliation de la vie professionnelle et de la vie privée pour médecins et femmes médecins des hôpitaux: Un guide pratique(Institut für Kooperationsforschung und -entwicklung, 05/2023) Frey, Julia; Kwakye, Delia; Liebig, Brigitte05 - Forschungs- oder ArbeitsberichtPublikation Conditions for spin-off creation at Swiss universities of applied sciences - a gender sensitive approach(Emerald, 22.06.2021) Blaese, Richard; Liebig, Brigitte; Schneider, NoemiPurpose The promotion of research-based entrepreneurship is considered a crucial task for universities and policymakers in many Western countries. Research has shown that the university environment plays a decisive role in the spin-off activities of researchers. Although the number of science-based spin-offs has increased in recent years, women are still an exception when it comes to developing spin-off ventures. In turn, there is a lack of knowledge regarding the university environment that supports entrepreneurship from a gender perspective. Design/methodology/approach Based on the theoretical framework of the “Entrepreneurial University,” this contribution examines the formal and informal conditions for academic entrepreneurship using the example of Swiss universities of applied sciences (UAS). Based on a cross-sectional dataset of 1,551 researchers from various disciplines who were surveyed in 2019, linear regressions and logistic regression models were used to test gender-specific differences in the perception of organizational conditions concerning the entrepreneurial exploitation of research. Findings The results demonstrated significant differences in the perception of formal and informal conditions in higher education. First, they show gender differences in the perception of informal entrepreneurial support in universities; in particular, female researchers received less informal support for spin-off projects. For example, women hardly viewed commercial use of research and development knowledge as a career option and considered the existence of entrepreneurial role models at universities to be low. Second, further analyses highlighted that also formal support offerings were less known among female researchers. Originality/value The study highlights organizational barriers for female researchers regarding the development of spin-off creation at UAS, including the different formal and informal conditions for female academics in comparison to their male counterparts.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Conditions for spin-offs at Swiss Universities of Applied Sciences(2019) Morandi, Pietro; Bläse, Richard; Schneider, Noemi; Liebig, Brigitte06 - PräsentationPublikation Conditions of Palliative Home Care: The Case of Family Physicians in Switzerland(Taylor & Francis, 2015) Alvarado, Vanessa; Liebig, BrigitteFamily physicians (FPs) play a key role in the treatment and care for terminally ill men and women. However, little is known about the conditions and challenges of FPs services in this domain. Aim of this article is to identify, how FPs can be supported in palliative home care in Switzerland by the availability of guidelines and advance directives, community-based palliative care structures, education and training, as well as remuneration of palliative home care services. Case studies in three Swiss cantons, namely Lucerne (LU), Vaud (VD), and Ticino (TI) are the basis of the following investigation. They not only represent French, Italian and German language regions but differ considerably with respect to the history of palliative care. Within and between cantons documents, questionnaires and expert interviews are analyzed thematically with the help of content-analysis. The results illustrate considerable shortcomings with respect to the backing of FPs palliative home care services. The availability and use of guidelines as well as advance directives is rather small in general practice, and FPs care and treatment at the end of life is only marginally supported by ambulant care structures, especially in rural areas. Also the coordination of services and collaboration between specialists and generalists is poorly developed. Furthermore FPs possibilities to acquire competencies in palliative care are strongly limited, and palliative home care provided by FPs is poorly financed. The results draw a rather bleak picture with respect to the support of FPs palliative home care services in Switzerland today. Though considerable steps towards implementing palliative care have been made in recent years in general, conditions for FPs medical services have to get improvedstrongly. Major efforts have to be made to foster the recognition and implementation throughout Switzerland.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Coordination and collaboration in primary palliative care: Palliative care networks in Switzerland(15.11.2021) Liebig, BrigitteEnabling chronically and terminally ill people to enjoy the best possible quality of life is the important goal of palliative care. This study provided valuable information about the requirements for service providers in the palliative care sector in order to provide the best possible support.06 - PräsentationPublikation Critical Transitions: The Production of Gender (In-)Equality in the Life Course(Emerald, 2015) Liebig, Brigitte; Levy, René01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Crossing boarders: Teamwork Related Challenges in Palliative Care(2019) Liebig, Brigitte; Reeves, Emily; Schweighoffer, Reka06 - PräsentationPublikation Das Toolkit mit (fast) unbegrenzten Möglichkeiten(31.08.2021) Mittner, Debora; Liebig, BrigitteDiversität ist ein Innovationstreiber – wenn die Bedingungen stimmen! Das Toolkit: Women & Diversity in Innovation beinhaltet Massnahmen und Instrumente zur Förderung von Diversität im Innovationsbereich. Seit Kurzem steht das Toolkit auf diversity-in-innovation.ch online zur Verfügung. Die folgenden Best-Practice-Beispiele geben Einblick, wie der Einsatz des Toolkit in der Praxis aussehen kann.01B - Beitrag in Magazin oder Zeitung