Conference Agenda

Overview and details of the sessions of this conference. Please select a date or location to show only sessions at that day or location. Please select a single session for detailed view (with abstracts and downloads if available).

 
 
Session Overview
Date: Tuesday, 22/Oct/2024
  E-posters: Overview of all e-posters
Please log in to view the e-posters
 

Effectiveness of palliative and hospice care basic training manual on non-health and health practitioners’ level of knowledge in the Philippines: A preliminary study

Edmar San Jose Elcarte, Agnes Bausa-Claudio, Lester Sam Geroy, Teddy Dizon, Ana Kristine Bermudez, Clarito Cairo. Jr.



Gender, family dynamics and end of life wishes

Lexi Bryony Sears



Reimagining death care for our ageing population

Rebecca Jane Lyons



Use and deprescribing of direct oral anticoagulants in Palliative C are

Federica Pica, Ursina Wernli, Constanze Rémi, Sibylle Jean-Petit-Matile, Christoph R. Meier, Carla Meyer-Massetti



The missing cancer and palliative care in displaced community in Northeast of India

Suryakanta Acharya



Rethinking palliative care from a sustainable perspective

Raffaella D'Orio, Camille Meyer



Development of a psychoeducation tool about dementia grief for German mental health providers

Lena Rupp, Christina Abele, Julia Haberstroh



Compassionate Communities for All from Children to the Elderly throughout Japan

Keiko Chida, Taketoshi Ozawa



Evaluating outcomes of ACP interventions for adults living with advanced illness and people close to them: a meta-review

Jodie Adele Crooks, Noura Rizk, Charlotte Simpson-Greene, Briony Hudson, Gina Hopwood, Kathy Seddon, Owen Smith



Reflections on co-producing palliative and end of life care research with co-researchers with lived experience of homelessness

Jodie Adele Crooks, Gareth Davis, Mandy Pattinson, Briony Hudson



The model development of compassionate community in Thailand from the study of Kalasin municipality compassionate community-based palliative care service for the end of life elderly patients and their families

Jiraphan Naruepatr



Celebrating Life: An innovative community engagement project with minoritized ethnic populations living in areas of socio-economic deprivation in North London: A Service Evaluation

Rekha Vijayshankar



Demographic profile of end of life family caregivers in the UK: an observational study

Clare Gardiner, Edward Webb, Arthur Juet, Juliet Stone



Pediatric palliative care needs in the Canton of Bern Switzerland

Brigitte Hofer, Eva Maria Tinner Oehler, Maya Zumstein-Shaha



Palliative Care Services Among Hospitalized Children with Serious and Life-Limiting Conditions in the U.S.

Jay Shen, Zahra Mojtahedi, Pearl Kim



Play needs of children with palliative care needs: a Q methodology study

Zainab A Jasem



The safari concept: an african framework for end of life care

Christian Ntizimira, Deo Mbonyinkebe, Mary Dunne



'It's more than rainbows in receptions' - Working with LGBTQ+ People in Palliative and End-of-Life Care

Gemma Allen, Jed Jerwood



A caregiver's coping process with the end-of-life care of a patient with cancer at home: a case study

Aya Yoshida, Kanami Takasuga, Yoriko Hara, Mika Yasue, Hiromi Matumoto, Yuka Suzaki



Advance care planning and palliative care for an adolescent with acute myeloid leukemia

Alma Lipnica Pabilane



Compassionate brereton and ravenhill

Sue Merriman, Emma Hodges



Developing Compassionate Community with ‘community connectors’

Kaori Yoshida



Facing Death

Matija Tomc, Hana Kodba Čeh, Špela Klara Jambrek, Alenka Križnik



Impact of an ‘End-of-Life Education’ Training Course on Knowledge and Attitudes of Nurses and Patient Care Assistants in a Nursing Home

Dilys Inqi Lee, Wan Ru Ng



Intergenerational Conversations about LGBTQ+ Needs at the End-of-Life – Reflections From Sweden

Max Kleijberg, Marion Englaborn, Lars E. Eriksson



Palliative care in the acute setting

Rebecca Newell



Quantifying clinical load and role for Generalist Palliative Care in COVID 19 patients results from a cohort study on the Predictors of High Opioid and Benzodiazepine use In COVID 19 patients (PHOBIC)

Mahrley Tanagon Provido, Wen Yang Goh, Sheryl Ng



Reflection from college students after a designed interactive speech of advance care planning: A qualitative study with theme analysis by large language model

Chia-Hsuan Chiang, Yu-Ju Lin, Yi-Ling Yeh, Shu Yi Wang, Shuh-Jen Sheu, Wei-Min Chu



At the End Diversity. A project to integrate volunteers with migration background into activities of a hospice movement in Germany.

Wilhelm Freiherr von Hornstein, Hildegard Bargenda, Mara Kaiser



Concern and care needs of older patients in South Australian rural public hospitals

Jaklin Ardath Eliott, Gregory Crawford, Kate Gunn, Gillian Harvey, Anna Chur-Hansen, Ann Dadich, Lucie Walters, Ali Lakhani, Timothy To, Linda Foreman



Cross-cultural equivalence of construct validity of the Death Literacy Index in Belgium, the Netherlands, and Sweden

Therese Johansson



Disparate trends in place of death for people with different cancer types: a national population–based study

Cecilia Larsdotter



End-of-life preferences among different forms of engagement in advance care planning

Carmen Borrat-Besson



EU Navigate training prepares navigators in European countries to support older persons with cancer living at home

Iris Beijer Veenman, Annicka van der Plas, Roeline Pasman, Wendy Duggleby, Barbara Pesut, Lieve van den Block, Katarzyna Szczerbinska, Barbara Gomes, Laura Gangeri, Andrew Davies, Davide Ferraris, Bregje Onwuteaka-Philipsen



Experiences of care in the last three months of life: findings from a nationally representative post-bereavement survey in England and Wales

Therese Johansson



How tattoos contribute to connection and healing

Susan Cadell, Stephanie Levac, Taitum MacAulay, Melissa Reid Lambert, Mary Ellen Macdonald



Place of Death Among Children: a population based study from Sweden

Stefan Nilsson, Joakim Öhlén, Stina Nyblom, Anneli Ozanne, Margaretha Stenmarker, Cecilia Larsdotter



Unsung heroes of COVID-19’: Funeral directors’ compassionate cultural care of bereaved Māori whānau and communities during COVID-19

Tess Huia Moeke-Maxwell, Jeanette Marie Scurr, Linda Waimaria Nikora



Working with communities: Helping you to live well as long as you can (promoting death literacy in ethnic minority communities)

Georgia Rowley, Ali Lakhani, Shyla Mills, Florine Fernandes, Helen Kyriazopoulos, Kerrie Noonan, Jaklin Ardath Eliott



PREPARE: Evaluation of Electronic Palliative Care Coordination Systems to support advance care planning for people living with life-threatening conditions: A retrospective observational cohort study

Marcel Alied, Sophie Law-Clucas, Joanne Droney, Ceire Costelloe, Christina Ramsenthaler, Matthew Allsop, Peter May, Katherine Sleeman, Julia Verne, Denzil James, Lisa Scerri, Diane Laverty, John Rosling, Margaret Powell, Alastair Bearne, Rashmi Kumar, Jonathan Koffman



"Palliative Care goes School" - Results from a Project for Upper School Classes in Vorarlberg

Andrea Moosbrugger, Otto Gehmacher, Fabian Rebitzer



A model of narrative medicine in palliative care: how to use it to create a compassionate city

Danila Zuffetti



Acceptance of illness and worry about dying and their association with faith and family support among advanced cancer patients

Maria Fidelis Coronel Manalo. MD



Comfort care order sets in ambulatory setting

Anu Mehra, Aurélie Tahar Chaouche, Petra Vayne-Bossert



Compassionate Bunbury Charter and Toolkit: Fostering community conversations and civic actions

Samar Aoun, Julieanne Hilbers



Creating Learning Communities. An international Training of Trainers course for the promotion of death literacy in three different countries

Patrick Schuchter, Marianne Buchegger, Johannes Jurka, Irina Adascalitei, Elena Gaicu, Ina Dreglea, Maria dos Anjos Dixe, Ana Querido, Carlos Laranjeira



Educational approaches toward teaching palliative care to non-palliative care physicians

Maria Fidelis Coronel Manalo. MD



Exploring a strengths-based approach: Challenging the deficit narrative in rural health research

Marylouise Freeman, Kate Gunn, Gemma Skaczkowski, Jason Mills



Governance and organisation of palliative care in cancer care in Sweden - cancer care leaders’ perspectives

Anna O'Sullivan, Joakim Öhlén, Stina Nyblom, Anneli Ozanne, Carl-Johan Fürst, Cecilia Larsdotter



Healing light: The healing journey through palliative care research

Yanisa Niennattrakul



On the way to Dementia Literacy - introducing the dementiafriendly 3rd district, Vienna

Marianne Buchegger



Palliative care in policy documents for adults with cancer and non cancer diseases with potential palliative care needs: A document analysis

Anna O'Sullivan, Linnéa Carling, Joakim Öhlén, Stina Nyblom, Anneli Ozanne, Ragnhild Hedman, Carl-Johan Fürst, Cecilia Larsdotter



Pediatric Palliative Care – building bridges between hospital and community care for child and family

Simone Keller, Brigitte Griffiths



Policies and advocacy toward upgrading the 2015 Philippine status from being the 3rd worst place to die in the world (78th out of 80 countries) to 38th place in the cross-country comparison of expert assessments of the Quality of Death and Dying 2021

Maria Fidelis Coronel Manalo. MD



Trends in the place of death for people with cardiovascular disease in Sweden 2013-2019 - a registry study

Stina Nyblom, Joakim Öhlén, Cecilia Larsdotter, Anneli Ozanne, Carl Johan Fürst, Ragnhild Hedman



If death was told to me - Youth literature as a creative means to discussing death

Deborah Ummel, Émilie Lauzière, Jessica Rassy

  Set 1: poster abstracts
 

Exploring the hope experience and quality of life among dyads of people and their informal caregivers living with chronic obstructive pulmonary disease in Switzerland: First results from qualitative data analysis

Filipa Alexandra Baptista Peixoto Befecadu, Zaria Gossin, Sofia Savinelli, Jérôme Stirnemann, Ivan Guerreiro, Cyril Jaksic, Tatiane Balbinotti, Alexandra Balmer, Ghislaine Behagel, Tanja Fusi-Schmidhauser, Gora Da Rocha Rodrigues, Philip Larkin, Sophie Pautex



A grassroots approach to Compassionate Communities

Emma Hodges, Sue Merrimen



Compassionate Libraries: building compassionate communities with our local libraries.

Maxine Zhong



Death Literacy in Australia: Did COVID-19 and the introduction of Voluntary Assisted Dying have an impact?

Kerrie Noonan, Andrea Grindrod, Sumina Shrestha, Sora Lee, Rosemary Leonard



Enhancing access to sexual and reproductive health services among indigenous people in earthquake-affected area of Jajarkot and West Rukum district, Nepal

Chet Raj Joshi



The Facing-Death Project - A Community-Based Collaborative Art Initiative to Enhance End-of-Life Care Engagement: a pilot study

Matija Tomc, Špela Klara Jambrek, Alenka Križnik, Hana Kodba Čeh



‘De Kolibrie’, a compassionate place

Ria Plasschaert



Perceived quality, difficulties, and needs for End-of-life care at home: Perspectives of Thai patients and family caregivers

Kittikorn Nilmanat, Samonnun Thasaneesuwan, Jintana Damkliang, Kallaya Sae-Chit, Pangpan Sriboonlue



How tattoos contribute to connection and healing

Susan Anne Cadell, Stephanie Levac, Taitum MacAulay, Mary Ellen Macdonald



Experiences of care service use in the last three months of life: findings from a national post-bereavement survey in England and Wales

Therese Johansson, Lucy Budd, Rachel L Chambers, Anna E Bone, Irene J Higginson, Stephen Barclay, Fliss E M Murtagh, Katherine E Sleeman



Acceptance of illness and worry about dying and their association with faith and family support among advanced cancer patients

Maria Fidelis Coronel Manalo, Macario Reandelar. Jr., Eric A. Finkelstein



Implementability of an evidence-informed BEereavement SupporT pathway in Swiss specialized palliative care (BEST for Family): Pre-implementation analysis of palliative care staff perceptions

Marco Riguzzi, Sina Gyarmathy, Torsten Schwalbach, David Blum, Noemi Lehmann, Mirjam Buschor-Bichsel, Patrizia Künzler-Heule, Rahel Naef



Challenging issues perceived by Japanese visiting nurses in implementing advance care planning and realizing death at home

Mitsuko Ushikubo, Maho Ishikawa, Satoko Yamaji, Misako Hori, Laura Brooks, Debra Kerr



Cultural identities in palliative care research: A critical reflection on defining and categorising minority ethnic groups in end-of-Life care

Inayah Uddin, Henry Llewellyn, Sarah Yardley, Paul Higgs



COMPASSIONATE CASCAIS Community project to promote the culture of compassionate care By Associação Oficina da Compaixão

Joana Tavares de Almeida, Beatriz Patricio



PREPARE: Evaluation of Electronic Palliative Care Coordination Systems to support advance care planning for people living with life-threatening conditions: A retrospective observational cohort study

Marcel Alied, Sophie Law-Clucas, Joanne Droney, Ceire Costelloe, Christina Ramsenthaler, Matthew Allsop, Peter May, Katherine Sleeman, Julia Verne, Denzil James, Lisa Scerri, Diane Laverty, John Rosling, Margaret Powell, Alastair Bearne, Rashmi Kumar, Jonathan Koffman



Perspectives on Needs and Barriers to Home-Based End-of-Life Care Delivery in Thailand

Kittikorn Nilmanat, Samonnan Thasaneesuwan, Jintana Damkliang, Kallaya Sae-chit, Paengpan Sribunlue



Developing accessible and culturally relevant palliative care education for Indigenous communities in Canada

Holly Prince, Jessica Wyatt



Using strengths-based approaches in rural health research and their application to improving the provision of rural palliative care: A scoping review.

Marylouise Freeman, Kate Gunn, Gemma Skackowski, Jason Mills



Intergenerational conversations about LGBTQ+ needs at the end-of-life – reflections from Sweden

Max Kleijberg, Marion Englaborn, Lars E. Eriksson



The model development of compassionate community in Thailand from the study of Kalasin municipality’s community-based palliative care service for the end of life elderly patients and their families

Jiraphan Naruepatr



Destigmatising palliative care within the peer group of young adults: Systematic review and ideas for interventions in the context of public health

Yann-Nicolas Batzler, Chantal Marazia, Manuela Schallenburger, Jacqueline Schwartz, Martin Neukirchen



Place of Death Among Children: a population-based study from Sweden

Stefan Nilsson, Joakim Öhlén, Stina Nyblom, Anneli Ozanne, Margaretha Stenmarker, Cecilia Larsdotter



End of life doulas and the value of death - communication, advocacy, presence

Annetta Helene Mallon



EU-Navigate training prepares navigators in European countries to support older persons with cancer living at home

Iris Beijer Veenman, Annicka van der Plas, Roeline Pasman, Wendy Duggleby, Barbara Pesut, Lieve van den Block, Katarzyna Szczerbinska, Barbara Gomes, Laura Gangeri, Andrew Davies, Davide Ferraris, Bregje Onwuteaka-Philipsen



Disparate trends in place of death for people with different cancer types: a national population-based study

Cecilia Larsdotter, Stina Nyblom, Anneli Ozanne, Carl-Johan Furst, Anna O´Sullivan, Joakim Öhlén



Compassionate Bunbury Charter and Toolkit - Fostering community conversations and civic actions

Julieanne Hilbers, Samar Aoun



Play needs of children living with palliative care needs: a Q methodology study

Zainab A Jasem, Danielle Lambrick, Duncan C Randall, Anne-Sophie Darlington



Overcoming challenges: Palliative care delivery for COPD patients in urban slums - Lessons learned and future directions

Kazi Sarmad Karim, Abida Sultana, Ritu Akhter, Mohd. Saiful Hoque Saif, Md Julhash Uddin



Caregiver burden, Anxiety, and Depression on the level of quality of life among primary caregivers of cancer patients in selected institutions in Metro Manila: An Explanatory Sequential Mixed Method Study

Edmar San Jose Elcarte



How to produce a health-oriented nursing practice in home-based palliative care? Results from a narrative inquiry

Jérôme Leclerc-Loiselle, Sylvie Gendron, Serge Daneault



Integration of Palliative Care in Nephrology: A benefit for patients and relatives as well as economically. What we can learn from Australia

Stefan Pelz, Kenneth Yong, Sara Stoller, David Blum, Meg Sands



Psychosocial Rehabilitation Trajectory of Stroke Survivors (PReTS): An overview of systematic reviews of recovery needs and non-death losses

Andy Hau Yan Ho, Muhahammad Amin Shaik, Paul Victor Patinadan, Geraldine Tan-Ho



End-of-life preferences among different forms of engagement in advance care planning

Carmen Borrat-Besson, Sarah Vilpert, Maud Wieczorek, Clément Meier, Robert Reinecke, Ralf J. Jox, Gian Domenico Borasio, Jürgen Maurer



Understanding how policies impact global access to and safe use of opioid medicines

Brandon Maser, Eve Namisango, Sumit Gupta, Jillian Kohler, Avram Denburg, Mark Dobrow



Advance Care Planning: Why are patients interested?

Esther Nafula Wekesa



At the End Diversity. A project to integrate volunteers with migration background into activities of a hospice movement in Germany.

Wilhelm Freiherr von Hornstein



Head, heart and hands - elements essential in community-focused education to support grieving young people

Alyson Jane Gundry, Quality of Care Collaborative Australia



The missing cancer and palliative care in displaced community in Northeast of India

Suryakanta Acharya



Palliative care-related knowledge, attitudes & confidence in home health care: Results from a U.S. pilot study

Ashley M. Chastain, Jingjing Shang, Lori King, Charity Ogunlusi, Komal P. Murali, Jung A. Kang, Khadra Dualeh, Suning Zhao, Margaret V. McDonald



Determinants of distress among cancer patients admitted for the day care treatment at a tertiary care Cancer hospital, Amritsar, Punjab.

Harjot Singh Birgi, Paramjot Bindra, Manisha Nagpal



Concerns and care needs of older patients in South Australian urban and rural public hospitals

Jaklin Ardath Eliott, Gregory Crawford, Kate Gunn, Gillian Harvey, Anna Chur-Hansen, Ann Dadich, Lucie Walters, Ali Lakhani, Timothy To, Linda Foreman



Partners in healing: fostering interdisciplinary dialogues about the role of spiritual care in healthcare

TJ Douglas, Rachel Rim, Ronald Adelman, Jon Overvold



Development of a psychoeducation tool about dementia grief for German mental health providers

Lena Rupp, Christina Abele, Prof. Dr. Julia Haberstroh



Communication styles that bring comfort during serious illness conversations: A Swiss wide study

Robert Staeck, Carsten Sauer, Steven M. Asch, Sofia C. Zambrano



Palliative care in the acute admission setting

Rebecca Newell, Paul Pascal Jones, Ellie Evans, Molly Stewart, Nicola Henawi, Rachel Craig, Philip Lodge



Use and deprescribing of direct oral anticoagulants in palliative care

Federica Pica, Ursina Wernli, Constanze Rémi, Sibylle Jean-Petit-Matile, Christophe R. Meier, Carla Meyer-Massetti



Working with communities: Helping you to live well as long as you can (promoting death literacy in ethnic minority communities)

Georgia Rowley, Ali Lakhani, Shyla Mills, Florine Fernandes, Helena Kyriazopoulos, Kerrie Noonan, Jaklin Ardath Eliott



Healing light exhibition: the healing journey through dementia research

Yanisa Niennattrakul



Policies and advocacy toward upgrading the 2015 Philippine status from being the 3rd worst place to die in the world (78th out of 80 countries) to 38th place in the cross-country comparison of expert assessments of the Quality of Death and Dying 2021

Maria Fidelis Coronel Manalo, Agnes Bausa Claudio



Person-centred palliative home care from patient- and carer-perspectives – a scoping review

Lotta Pham, Malin Bengtsson, Jeanette Källstrand



Advanced training program in Spiritual Care Competence: insights from Spirituality Ibero-American Forum

María Nabal-Vicuña, Enric Benito, Marcela Specos, Ana Querido, Monica Dones, Carlos Laranjeira, Noemi Sanso



Comfort care order sets in an ambulatory setting

Anu Mehra, Aurélie Tahar Chaouche, Petra Vayne-Bossert



Public-facing education of an early palliative care approach: Impacts of the Waiting Room Revolution social movement

Hsien Seow, Samantha Winemaker

9:30am
-
10:30am
Registration
Location: Bühnen Bern city theater / Stadttheater
10:30am
-
11:00am
Welcoming ceremony
Location: Bühnen Bern city theater / Stadttheater
11:00am
-
12:30pm
Plenary 1: Connections - from compassion to self-compassion to clinical care
Location: Bühnen Bern city theater / Stadttheater
Chair: Philip J Larkin, CHUV /University of Lausanne, Switzerland
Chair: Jason Mills, Flinders University, Australia
Chair: Sofia C. Zambrano, University of Bern, Switzerland
Language: English
12:30pm
-
2:00pm
Lunch break
Location: Kornhauskeller
2:00pm
-
3:30pm
Plenary 2: Death literacy - how to develop, how to measure
Location: Kornhausforum - Plenary hall
Chair: Joachim Cohen, Vrije Universiteit Brussel, Belgium
Chair: Ekkapop Sittiwantana, Compassionate Communities Research and Devlopment Institution Foundation Thailand, Thailand
Chair: Carol Tishelman, Karolinska Institutet, Sweden
Language: English
3:30pm
-
4:00pm
Coffee break
Location: Kornhauskeller
4:00pm
-
5:30pm
D-A-CH session 1: Die Care-Transformation in den DACH-Ländern … auf dem Weg zum gemeinsamen Verständnis.
Location: Le Cap - Room "Nicolas Manuel"
Chair: Raymond Voltz, University Hospital Köln, Germany
Chair: Veronika Schönhofer-Nellessen, Bildungswerk Aachen, Germany
Language: German
 

Ein Buddy als zusätzliche Ressource in der Versorgung schwer und unheilbar erkrankter Menschen: Ergebnisse qualitativer Interviews mit Betroffenen und Versorgenden

Alina Kasdorf, Raymond Voltz, Julia Strupp



Improving Death Literacy in a Community: A systematic Approch

Raymond Voltz, Georg Bollig, Heidrun Golla, Kerstin Kremeike, Steffen Simon, Julia Strupp



Enhancing end-of-life care through community engagement and research – a study protocol

Maria Heckel, Saskia Kauzner, Manuela Schneider, Carsten Klein, Christoph Ostgathe



Young people discovering death, dying and grief – How dialogue culture could pave the way for voluntary work in hospice care

Bernadette Groebe, Klaus Wegleitner, Patrick Schuchter, Dirk Blümke



Caring Community Köln – lessons learnt so far

Karin Ohler, Birgit Weihrauch, Sabine Eichberg, Anne Kreische, Julia Strupp, Raymond Voltz

Parallel Session 1a: Building equity
Location: Kornhausforum - Plenary hall
Chair: Therese Johansson, King's College London, United Kingdom
Chair: Stephen Robert Connor, Worldwide Hospice Palliative Care Alliance, United States of America
Language: English
 

The impact of area deprivation on access to and utilization of health services in the last year of life: a retrospective population based cohort study

Jackie Robinson, Bert van der Werf, Daniel Exeter, Jinfeng Zhao, Janine Wiles, Merryn Gott



“I don’t know what options there are”: Indigenous families’ experiences with cancer and assisted dying in Aotearoa New Zealand

Tess Huia Moeke-Maxwell, Jackie Robinson, Lisa Williams, Jeanette Scurr, Tau Huirama



What matters to Pakistani women during dying, death, grief and caring at the end-of-life: an intersectional participatory study

Mariam Fargin, Inayah Sher, Shabina Bashir, Samina Begum, Jamilla Hussain



Developing the Intervention to optiMise Palliative caRe for peOple with liVed Experience of homelessness (IMPROVE)

Briony Hudson, Caroline Shulman



"Living well until the end" - promoting death literacy for older people with a migration biography and/or a precarious socio-economic background

Anna-Christina Kainradl, Klaus Wegleitner

Parallel session 1b: Supporting professional caregivers
Location: Hotel Bern - Room "Unionssaal 1"
Chair: Sofia C. Zambrano, University of Bern, Switzerland
Chair: Luc Deliens, Vrije Universiteit Brussel, Belgium
Language: English
 

Absence of grief care: Japanese medical professionals have no place to grieve

Aki Morita



We are all mortals – Undergraduate nursing students’ reflections following a seminar focused on proactive end-of-life communication

Malin Eneslätt, Ingela Jobe, Catharina Melander



Increasing access to primary palliative care through undergraduate education: New Zealand medical and nursing graduates’ preparation, self-efficacy and attitudes towards providing palliative and end-of-life care.

Elisabeth Ellen Heath, Richard Egan, Ella Iosua, Robert Walker, Jean Ross, Rod MacLeod



Developing an appropriate model of palliative care for mainland China: exploring the application of alternative medicine in the Shanghai model

Chenyang Guo, Xinyan Cheng



"If death was told to me": Youth literature as a creative means to discussing death

Deborah Ummel, Émilie Lauzière, Rassy Jessica

Parallel session 1c: Experiences of dying
Location: Hotel Bern - Room "Unionssaal 2"
Chair: Kelli Stajduhar, University of Victoria, Canada
Chair: Bert Quintiens, Vrije Universiteit Brussel, Belgium
Language: English
 

How culture shapes the relationship to death: towards an anthropological theory to track social and cultural transformations in public health approaches to death and dying

Émilie Lessard



The meaning of good death among Thai people

Penchan Pradubmook sherer



“Sorry to make you think my life is a misery but I am content”: Experiences and Perceptions of Social Wellbeing among Adults Living with Advanced Illness.

Mary Kimani, Fliss E M Murtagh, Slavica Kochovska, Liz Walker



Revisiting Ars moriendi and Ars memorandi. End-of-Life Narratives and spiritual Meaning and legacy-making in western european end-of-Life Care.

Zoë Ghyselinck



‘Wanting to be Heard’ – A Qualitative Study of Patients’ and Nominated Healthcare Spokespersons’ Experiences of Goals of Care Discussions in Acute Care

Joshua Shaowen Lee, Katrielle Joy Xiyue Fu, Lynn Wiryasaputra, Celestine Zi Qian Lim, Paul Victor Patinadan, Yew Jin Ong, Andy Hau Yan Ho, Tricia Sek Hwee Yung

Workshop 1a: “What if our last breaths could be breathtaking?”: A “walkshop” exploring parks/nature connection in palliative and grief care
Location: Hotel Kreuz - Room "Hodler"
Language: English
 

“What if our last breaths could be breathtaking?”: A “walkshop” exploring parks/nature connection in palliative and grief care

Sonya L. Jakubec, Jennell Rempel

Workshop 1b: Connecting communities in palliative care: Using a design science approach for co-developing humility guidance
Location: Hotel Kreuz - Room "Fischer"
Language: English
 

Connecting communities in palliative care: Using a design science approach for co-developing humility guidance

Rachel Coghlan, Sartre Ndebaneza, Gary Witham, Carey Candrian, Rebecca Wright

Workshop 1c: How to use storytelling and gamification to communicate complex realities? The case of the Stay Room™ and palliative care
Location: Le Cap - Room "Arche/Refuge"
Language: English
 

How to use storytelling and gamification to communicate complex realities? The case of the Stay Room™ and palliative care

Ana Paula Salas Moreira, Beatriz Gomez Baceiredo

 
5:30pm
-
6:00pm
Break
6:00pm
-
8:00pm
Free classical concert: "Building Bridges"
Location: French Church / Französische Kirche
Free concert for all participants and the people from Bern and around. The concert takes place in the Französische Kirche Bern (French Church Bern) - with the choir of the Kirchenfeld Gymnasium Bern - with the instrumental ensemble of the Kirchenfeld Gymnasium Bern - with the cello quartet of the Swiss Medical Orchestra SMO - with Martin Hostettler, tenor

 
Contact and Legal Notice · Contact Address:
Privacy Statement · Conference: PHPCI 2024
Conference Software: ConfTool Pro 2.8.105+CC
© 2001–2025 by Dr. H. Weinreich, Hamburg, Germany