200 related articles for article (PubMed ID: 25994479)
21. [Family caregivers of palliative cancer patients: health-related quality of life and care-related burden].
Köhler N; Perner A; Anders D; Brähler E; Papsdorf K; Götze H
Psychother Psychosom Med Psychol; 2012 May; 62(5):157-62. PubMed ID: 22441884
[TBL] [Abstract][Full Text] [Related]
22. The stress process in palliative cancer care: a qualitative study on informal caregiving and its implication for the delivery of care.
Brazil K; Bainbridge D; Rodriguez C
Am J Hosp Palliat Care; 2010 Mar; 27(2):111-6. PubMed ID: 20008823
[TBL] [Abstract][Full Text] [Related]
23. Evaluation of a psycho-educational group programme for family caregivers in home-based palliative care.
Hudson P; Quinn K; Kristjanson L; Thomas T; Braithwaite M; Fisher J; Cockayne M
Palliat Med; 2008 Apr; 22(3):270-80. PubMed ID: 18477722
[TBL] [Abstract][Full Text] [Related]
24. Reducing the psychological distress of family caregivers of home-based palliative care patients: short-term effects from a randomised controlled trial.
Hudson P; Trauer T; Kelly B; O'Connor M; Thomas K; Summers M; Zordan R; White V
Psychooncology; 2013 Sep; 22(9):1987-93. PubMed ID: 23335153
[TBL] [Abstract][Full Text] [Related]
25. [Caregiver burden in relatives of persons with schizophrenia: an overview of measure instruments].
Reine G; Lancon C; Simeoni MC; Duplan S; Auquier P
Encephale; 2003; 29(2):137-47. PubMed ID: 14567165
[TBL] [Abstract][Full Text] [Related]
26. Experience of palliative home care according to caregivers' and patients' ages in Hong Kong Chinese people.
Chan CW; Chang AM
Oncol Nurs Forum; 2000; 27(10):1601-5. PubMed ID: 11103379
[TBL] [Abstract][Full Text] [Related]
27. Perceived caregiving preparedness and quality of life among Indonesian family caregivers of patients with life-limiting illness.
Rochmawati E; Prawitasari Y
Int J Palliat Nurs; 2021 Aug; 27(6):293-301. PubMed ID: 34459242
[TBL] [Abstract][Full Text] [Related]
28. Costs of Family Caregiving in Palliative Care (COFAC) questionnaire: development and piloting of a new survey tool.
Gardiner C; McDermott C; Hulme C
BMJ Support Palliat Care; 2019 Sep; 9(3):300-306. PubMed ID: 28213346
[TBL] [Abstract][Full Text] [Related]
29. Mutuality and preparedness moderate the effects of caregiving demand on cancer family caregiver outcomes.
Schumacher KL; Stewart BJ; Archbold PG
Nurs Res; 2007; 56(6):425-33. PubMed ID: 18004189
[TBL] [Abstract][Full Text] [Related]
30. Quality of life and mental health in caregivers of outpatients with advanced cancer.
Wadhwa D; Burman D; Swami N; Rodin G; Lo C; Zimmermann C
Psychooncology; 2013 Feb; 22(2):403-10. PubMed ID: 22135229
[TBL] [Abstract][Full Text] [Related]
31. Measuring the regret of bereaved family members regarding the decision to admit cancer patients to palliative care units.
Shiozaki M; Hirai K; Dohke R; Morita T; Miyashita M; Sato K; Tsuneto S; Shima Y; Uchitomi Y
Psychooncology; 2008 Sep; 17(9):926-31. PubMed ID: 18157913
[TBL] [Abstract][Full Text] [Related]
32. Development and initial validation of a family appraisal of caregiving questionnaire for palliative care.
Cooper B; Kinsella GJ; Picton C
Psychooncology; 2006 Jul; 15(7):613-22. PubMed ID: 16287207
[TBL] [Abstract][Full Text] [Related]
33. Palliative family caregivers' accounts of health care experiences: the importance of "security".
Funk LM; Allan DE; Stajduhar KI
Palliat Support Care; 2009 Dec; 7(4):435-47. PubMed ID: 19939306
[TBL] [Abstract][Full Text] [Related]
34. Determinants of a hopeful attitude among family caregivers in a palliative care setting.
Kim SY; Kim JM; Kim SW; Kang HJ; Shin IS; Shim HJ; Cho SH; Chung IJ; Yoon JS
Gen Hosp Psychiatry; 2014; 36(2):165-71. PubMed ID: 24342114
[TBL] [Abstract][Full Text] [Related]
35. Explaining family caregiver role strain following autologous blood and marrow transplantation.
Eldredge DH; Nail LM; Maziarz RT; Hansen LK; Ewing D; Archbold PG
J Psychosoc Oncol; 2006; 24(3):53-74. PubMed ID: 17088241
[TBL] [Abstract][Full Text] [Related]
36. Family caregiving in advanced chronic organ failure.
Janssen DJ; Spruit MA; Wouters EF; Schols JM
J Am Med Dir Assoc; 2012 May; 13(4):394-9. PubMed ID: 21621478
[TBL] [Abstract][Full Text] [Related]
37. Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers.
Holm M; Carlander I; Fürst CJ; Wengström Y; Årestedt K; Öhlen J; Henriksson A
BMC Palliat Care; 2015 Apr; 14():16. PubMed ID: 25903781
[TBL] [Abstract][Full Text] [Related]
38. Experiences of the older spousal caregivers of patients with cancer during palliative chemotherapy: a qualitative descriptive study.
Hirayama K; Kuribara T; Oshikiri M
BMC Palliat Care; 2023 Nov; 22(1):188. PubMed ID: 37993823
[TBL] [Abstract][Full Text] [Related]
39. Development and testing of a measure of perceived caregiver rewards in adults.
Picot SJ; Youngblut J; Zeller R
J Nurs Meas; 1997; 5(1):33-52. PubMed ID: 9505468
[TBL] [Abstract][Full Text] [Related]
40. Identifying socio-environmental factors that facilitate resilience among Canadian palliative family caregivers: a qualitative case study.
Giesbrecht M; Wolse F; Crooks VA; Stajduhar K
Palliat Support Care; 2015 Jun; 13(3):555-65. PubMed ID: 24477169
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]