Literature DB >> 11251956

The role of social and psychologic resources in caregiving of cancer patients.

C Nijboer1, R Tempelaar, M Triemstra, G A van den Bos, R Sanderman.   

Abstract

BACKGROUND: The role of social support and personality within the cancer caregiving process has remained a relatively unexplored area. The current longitudinal study examines the main and moderating effects on caregiver experiences and caregiver's depression over time of various social and psychologic resources.
METHODS: Newly diagnosed colorectal carcinoma patients and their partners (N = 148) were included and data were obtained at three measurement points: 2 weeks prior to hospital admission and 3 months and 6 months after discharge. The initial and change scores of the caregiver's negative and positive social interactions and personality attributes (mastery, neuroticism, and extraversion) were included to assess their impact on caregiver experiences and depression over time.
RESULTS: The main effects of social and psychologic resources on caregiver experiences were found to be small to absent. With respect to caregiver depression, both initial scores and changes in neuroticism, mastery, and negative social interactions were shown to have substantial main effects over time. Moreover, daily emotional support and mastery modified the relations between caregiver experiences and caregiver depression. Caregivers with a low level of daily emotional support, as well as those with a low score on mastery and who also perceived caregiving in a more negative way were identified as more depressed over time.
CONCLUSIONS: The results of the current study demonstrate the importance of including various social and psychologic resources in studying the cancer caregiving process. It illustrates the distinctive impact of these resources on the depression of caregivers of patients with cancer, and therefore helps healthcare providers understand why some persons adapt better than others to their caregiving role. Copyright 2001 American Cancer Society.

Entities:  

Mesh:

Year:  2001        PMID: 11251956

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  56 in total

1.  Walking a mile in their shoes: anxiety and depression among partners and caregivers of cancer survivors at 6 and 12 months post-diagnosis.

Authors:  Sylvie D Lambert; Afaf Girgis; Christophe Lecathelinais; Fiona Stacey
Journal:  Support Care Cancer       Date:  2012-06-03       Impact factor: 3.603

2.  Burden of caregiving amongst family caregivers of patients with eating disorders.

Authors:  Angel Padierna; Josune Martín; Urko Aguirre; Nerea González; Pedro Muñoz; José Ma Quintana
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2012-06-22       Impact factor: 4.328

3.  Emotion regulation therapy for cancer caregivers-an open trial of a mechanism-targeted approach to addressing caregiver distress.

Authors:  Allison J Applebaum; Aliza A Panjwani; Kara Buda; Mia S O'Toole; Michael A Hoyt; Adam Garcia; David M Fresco; Douglas S Mennin
Journal:  Transl Behav Med       Date:  2020-05-20       Impact factor: 3.046

Review 4.  The cancer family caregiving experience: an updated and expanded conceptual model.

Authors:  Barbara Swore Fletcher; Christine Miaskowski; Barbara Given; Karen Schumacher
Journal:  Eur J Oncol Nurs       Date:  2011-10-14       Impact factor: 2.398

5.  Is a family equal to the sum of its parts: a comment.

Authors:  Ann M Holmes
Journal:  Qual Life Res       Date:  2005-05       Impact factor: 4.147

Review 6.  Physical, psychosocial, relationship, and economic burden of caring for people with cancer: a review.

Authors:  Afaf Girgis; Sylvie Lambert; Claire Johnson; Amy Waller; David Currow
Journal:  J Oncol Pract       Date:  2012-12-04       Impact factor: 3.840

7.  Trajectories of fatigue in family caregivers of patients undergoing radiation therapy for prostate cancer.

Authors:  Barbara A Swore Fletcher; Karen L Schumacher; Marylin Dodd; Steven M Paul; Bruce A Cooper; Kathryn Lee; Claudia West; Bradley E Aouizerat; Patrick S Swift; William Wara; Christine Miaskowski
Journal:  Res Nurs Health       Date:  2009-04       Impact factor: 2.228

8.  Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care.

Authors:  Heide Götze; Elmar Brähler; Lutz Gansera; Nina Polze; Norbert Köhler
Journal:  Support Care Cancer       Date:  2014-05-09       Impact factor: 3.603

9.  Depression and family interaction among low-income, predominantly hispanic cancer patients: a longitudinal analysis.

Authors:  Hyunsung Oh; Kathleen Ell; Andrew Subica
Journal:  Support Care Cancer       Date:  2013-10-04       Impact factor: 3.603

10.  How does a cancer education program impact on people with cancer and their family and friends?

Authors:  Georgina Sutherland; Louisa Hoey Dpsych; Victoria White; Michael Jefford; Suzanne Hegarty
Journal:  J Cancer Educ       Date:  2008       Impact factor: 2.037

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