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"Saying goodbye all alone with no close support was difficult"- Dying during the COVID-19 pandemic: an online survey among bereaved relatives about end-of-life care for patients with or without SARS-CoV2 infection

BMC health services research, 2021-09, Vol.21 (1), p.998-998, Article 998

2021

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What Keeps the Family Caregiver Motivated to Care for Their Dying Relative at Home? A Brief Report of a Qualitative Interview Study

Palliative medicine reports, 2024-05, Vol.5 (1), p.21-205

2024

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"My life became more meaningful": confronting one's own end of life and its effects on well-being-a qualitative study

BMC palliative care, 2022-04, Vol.21 (1), p.58-58, Article 58

2022

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"My everyday life has returned to normal"- Experiences of patients and relatives with a palliative day care clinic: a qualitative evaluation study

BMC palliative care, 2023-03, Vol.22 (1), p.26-26, Article 26

2023

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Quality of care in the last year of life: adaptation and validation of the German “Views of Informal Carers’ Evaluation of Services – Last Year of Life – Cologne”

BMC health services research, 2022-11, Vol.22 (1), p.1-1433, Article 1433

2022

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"Such an institution represents the circle of life" - bringing an inpatient hospice into an academic setting: a pre-implementation exploratory study

BMC palliative care, 2023-07, Vol.22 (1), p.96-96, Article 96

2023

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What are the risk factors for avoidable transitions in the last year of life? A qualitative exploration of professionals' perspectives for improving care in Germany

BMC health services research, 2021-02, Vol.21 (1), p.147-10, Article 147

2021

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Improving regional care in the last year of life by setting up a pragmatic evidence-based Plan–Do–Study–Act cycle: results from a cross-sectional survey

BMJ open, 2020-11, Vol.10 (11), p.e035988-e035988

2020

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Implementation of patient-centred care: which system-level determinants matter from a decision maker’s perspective? Results from a qualitative interview study across various health and social care organisations

BMJ open, 2021-09, Vol.11 (9), p.e050054-e050054

2021

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Top-down and bottom-up or participation through action? How to build a compassionate community - the experience of Caring Community Cologne

Palliative care and social practice, 2024-01, Vol.18, p.26323524241238230-26323524241238230

2024

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Live well, die well – an international cohort study on experiences, concerns and preferences of patients in the last phase of life: the research protocol of the iLIVE study

BMJ open, 2022-08, Vol.12 (8), p.e057229

2022

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Konfrontation mit der eigenen Endlichkeit

Psychotherapie im Alter, 2023-11, Vol.20 (4), p.435-446

2023

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Mitbetreuung von Angehörigen in spezifischen Versorgungsformen und der Pandemie: Ein Überblick über neue Erkenntnisse aus der Forschung in Deutschland – Teil 2

Zeitschrift für Palliativmedizin, 2024-09, Vol.25 (5), p.224-228

2024

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Der zeitliche Gesamtaufwand für den Hausarzt sinkt“: Die Sicht der Zuweisenden auf eine palliativmedizinische Tagesklinik

Zeitschrift für Evidenz, Fortbildung und Qualität im Gesundheitswesen, 2023-12, Vol.182-183, p.38-43

2023

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Dying at home: What is needed? Findings from a nationwide retrospective cross-sectional online survey of bereaved people in Germany

Palliative & supportive care, 2024-03, p.1-9

2024

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Palliativ and Todeswunsch

1, 2023

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Bedürfnisse, Probleme und Bedarfe von Angehörigen in der Palliativversorgung: Ein Überblick über neue Erkenntnisse aus der Forschung in Deutschland – Teil 1

Zeitschrift für Palliativmedizin, 2024-07, Vol.25 (4), p.172-175

2024

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The Buddy intervention: designing an additional support system for the last year of life. Qualitative insights from triangulated interviews and focus group discussions

Journal of public health, 2024-10, Vol.32 (10), p.2001-2013

2024

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Erfolgreiches Altern von Menschen mit Körperbehinderung: Das Kohärenzgefühl als Ressource? 1. Aufl., neue Ausg

Strupp, Julia

2011

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How to Talk About Attitudes Toward the End of Life: A Qualitative Study

American journal of hospice & palliative medicine, 2019-08, Vol.36 (8), p.697-704

2019

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The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review

Palliative Medicine, 2021-12, Vol.35 (10), p.1793-1814

2021

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Quality of health care for patients with coronary heart disease and comorbid mental disorders: a prospective cohort study

BMC Psychology, 2024-05, Vol.12 (1), p.288-288, Article 288

2024

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‘I see the high level of interpersonal support during the pandemic as proof that the good in people prevails’: the COVID-19 pandemic as a catalyst for building a caring community?

Journal of public health (Oxford, England), 2024-02, Vol.46 (1), p.175-184

2024

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"Saying goodbye all alone with no close support was difficult"- Dying during the COVID-19 pandemic: an online survey among bereaved relatives about end-of-life care for patients with or without SARS-CoV2 infection

What Keeps the Family Caregiver Motivated to Care for Their Dying Relative at Home? A Brief Report of a Qualitative Interview Study

"My life became more meaningful": confronting one's own end of life and its effects on well-being-a qualitative study

"My everyday life has returned to normal"- Experiences of patients and relatives with a palliative day care clinic: a qualitative evaluation study

Quality of care in the last year of life: adaptation and validation of the German “Views of Informal Carers’ Evaluation of Services – Last Year of Life – Cologne”

"Such an institution represents the circle of life" - bringing an inpatient hospice into an academic setting: a pre-implementation exploratory study

What are the risk factors for avoidable transitions in the last year of life? A qualitative exploration of professionals' perspectives for improving care in Germany

Improving regional care in the last year of life by setting up a pragmatic evidence-based Plan–Do–Study–Act cycle: results from a cross-sectional survey

Implementation of patient-centred care: which system-level determinants matter from a decision maker’s perspective? Results from a qualitative interview study across various health and social care organisations

Top-down and bottom-up or participation through action? How to build a compassionate community - the experience of Caring Community Cologne

Communication, Coordination, and Security for People with Multiple Sclerosis (COCOS-MS): a randomised phase II clinical trial protocol

Live well, die well – an international cohort study on experiences, concerns and preferences of patients in the last phase of life: the research protocol of the iLIVE study

Konfrontation mit der eigenen Endlichkeit

Mitbetreuung von Angehörigen in spezifischen Versorgungsformen und der Pandemie: Ein Überblick über neue Erkenntnisse aus der Forschung in Deutschland – Teil 2

Der zeitliche Gesamtaufwand für den Hausarzt sinkt“: Die Sicht der Zuweisenden auf eine palliativmedizinische Tagesklinik

Dying at home: What is needed? Findings from a nationwide retrospective cross-sectional online survey of bereaved people in Germany

Palliativ and Todeswunsch

Bedürfnisse, Probleme und Bedarfe von Angehörigen in der Palliativversorgung: Ein Überblick über neue Erkenntnisse aus der Forschung in Deutschland – Teil 1

The Buddy intervention: designing an additional support system for the last year of life. Qualitative insights from triangulated interviews and focus group discussions

Erfolgreiches Altern von Menschen mit Körperbehinderung: Das Kohärenzgefühl als Ressource? 1. Aufl., neue Ausg

Palliativ & Todeswunsch

How to Talk About Attitudes Toward the End of Life: A Qualitative Study

The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review

Quality of health care for patients with coronary heart disease and comorbid mental disorders: a prospective cohort study

‘I see the high level of interpersonal support during the pandemic as proof that the good in people prevails’: the COVID-19 pandemic as a catalyst for building a caring community?

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