Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Bausewein, Claudia
Daveson, Barbara A
Currow, David C
Downing, Julia
Deliens, Luc
Radbruch, Lukas
Defilippi, Kath
Lopes Ferreira, Pedro
Costantini, Massimo
Harding, Richard
and
Higginson, Irene J
2016.
EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services – Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement.
Palliative Medicine,
Vol. 30,
Issue. 1,
p.
6.
Pope, Natalie D.
Baldwin, Paula K.
and
Lee, Jacquelyn J.
2018.
“I Didn’t Expect to Learn as Much as I Did”: Rewards of Caregiving in Young Adulthood.
Journal of Adult Development,
Vol. 25,
Issue. 3,
p.
186.
Ewertzon, Mats
Alvariza, Anette
Winnberg, Elisabeth
Leksell, Janeth
Andershed, Birgitta
Goliath, Ida
Momeni, Pardis
Kneck, Åsa
Skott, Maria
and
Årestedt, Kristofer
2018.
Adaptation and evaluation of the Family Involvement and Alienation Questionnaire for use in the care of older people, psychiatric care, palliative care and diabetes care.
Journal of Advanced Nursing,
Vol. 74,
Issue. 8,
p.
1839.
Anderson, Eric W.
and
White, Katie M.
2018.
“It Has Changed My Life”: An Exploration of Caregiver Experiences in Serious Illness.
American Journal of Hospice and Palliative Medicine®,
Vol. 35,
Issue. 2,
p.
266.
Sherman, Deborah Witt
2019.
A Review of the Complex Role of Family Caregivers as Health Team Members and Second-Order Patients.
Healthcare,
Vol. 7,
Issue. 2,
p.
63.
Vermorgen, Maarten
De Vleminck, Aline
Leemans, Kathleen
Van den Block, Lieve
Van Audenhove, Chantal
Deliens, Luc
and
Cohen, Joachim
2020.
Family carer support in home and hospital: a cross-sectional survey of specialised palliative care.
BMJ Supportive & Palliative Care,
Vol. 10,
Issue. 4,
p.
e33.
Alvariza, Anette
Häger-Tibell, Louise
Holm, Maja
Steineck, Gunnar
and
Kreicbergs, Ulrika
2020.
Increasing preparedness for caregiving and death in family caregivers of patients with severe illness who are cared for at home – study protocol for a web-based intervention.
BMC Palliative Care,
Vol. 19,
Issue. 1,
Hajihosseini, Fatemeh
and
Nazari, Roghieh
2020.
The perception of nursing students of providing patients with fundamental nursing care: “Both good and bad”.
Journal of Nursing and Midwifery Sciences,
Vol. 7,
Issue. 3,
p.
180.
Mei, Yong-xia
Lin, Bei-lei
Zhang, Wei-hong
Wang, Shan-shan
Zhang, Zhen-xiang
Yang, Dong-bin
and
Cheung, Daphne Sze Ki
2020.
Creating a Caregiver Benefit Finding Scale of Family Caregivers of Stroke Survivors: Development and Psychometric Evaluation.
Frontiers in Psychiatry,
Vol. 11,
Issue. ,
Tsuboi, Hirohito
Sakakibara, Hiroyuki
Matsunaga, Masahiro
Tatsumi, Asami
Yamakawa-Kobayashi, Kimiko
Yoshida, Naoko
and
Shimoi, Kayoko
2020.
Omega-3 Eicosapentaenoic Acid Is Related to Happiness and a Sense of Fulfillment—A Study among Female Nursing Workers.
Nutrients,
Vol. 12,
Issue. 11,
p.
3462.
Lin, Christopher J.
Cheng, Yao I.
Garvie, Patricia A.
D’Angelo, Lawrence J.
Wang, Jichuan
and
Lyon, Maureen E.
2020.
The Effect of FAmily-CEntered (FACE®) Pediatric Advanced Care Planning Intervention on Family Anxiety: A Randomized Controlled Clinical Trial for Adolescents With HIV and Their Families.
Journal of Family Nursing,
Vol. 26,
Issue. 4,
p.
315.
Becqué, Yvonne N.
Rietjens, Judith A. C.
van der Heide, Agnes
and
Witkamp, Erica
2021.
How nurses support family caregivers in the complex context of end-of-life home care: a qualitative study.
BMC Palliative Care,
Vol. 20,
Issue. 1,
Beng, Tan Seng
Ying, Yeoh Kee
Xin, Cheah Ai
Jane, Lim Ee
Lin, Dong Chooi
Khuen, Lim Poh
Capelle, David Paul
Zainuddin, Sheriza Izwa
Chin, Loh Ee
and
Loong, Lam Chee
2021.
The experiences of well-being of family caregivers in palliative care: A qualitative study using thematic analysis.
Progress in Palliative Care,
Vol. 29,
Issue. 4,
p.
209.
Watson, Jack D.
Perrin, Paul B.
McDonald, Scott D.
Tyler, Carmen M.
Burke, Julian
Pierce, Bradford S.
Hugeback, Hannah
and
Mickens, Melody N.
2021.
Research Participant Recruitment Strategies Among Individuals with Acute Spinal Cord Injury and Their Caregivers.
Spine,
Vol. 46,
Issue. 16,
p.
1111.
van Driel, Anne Geert
Becqué, Yvonne
Rietjens, Judith A.C.
van der Heide, Agnes
and
Witkamp, Frederika E.
2021.
Supportive nursing care for family caregivers – A retrospective nursing file study.
Applied Nursing Research,
Vol. 59,
Issue. ,
p.
151434.
Wind, Gitte
Vedsegaard, Helle Wendner
Marsaa, Kristoffer
True, Trine Solander
and
Konradsen, Hanne
2022.
The significance of the COVID-19 pandemic for family caregivers of non-COVID-19 patients in need of specialized palliative care at home: a qualitative study.
International Journal of Qualitative Studies on Health and Well-being,
Vol. 17,
Issue. 1,
Gascon Depatie, Marjolaine
and
Houle, Janie
2022.
EXPÉRIENCE DES PROCHES AIDANTS D’UNE PERSONNE VIVANT UN PREMIER ÉPISODE TROUBLE DÉPRESSIF CARACTÉRISÉ.
Revue québécoise de psychologie,
Vol. 43,
Issue. 1,
p.
111.
Van Goethem, Vincent
Dierickx, Sigrid
Deliens, Luc
De Vleminck, Aline
Lapeire, Lore
and
Cohen, Joachim
2023.
Size and characteristics of family caregiving for people with serious illness: A population-based survey.
Palliative and Supportive Care,
Vol. 21,
Issue. 4,
p.
634.
Shahbaz, Reemal
Williams, Allison
Sethi, Bharati
and
Wahoush, Olive
2023.
Commonalities and Differences in the Experiences of Visible Minority Transnational Carer–Employees: A Qualitative Study.
International Journal of Environmental Research and Public Health,
Vol. 20,
Issue. 18,
p.
6800.
Sarradon-Eck, Aline
Mathiot, Aurelia
Holmes, Seth M.
Gilbert, Elise
Capodano, Géraldine
Proux, Aurélien
and
Custers, Jose
2023.
The Moral Dimensions of Family Caregiving for Patients with Advanced Cancer: A Qualitative Study.
European Journal of Cancer Care,
Vol. 2023,
Issue. ,
p.
1.