Literature DB >> 12854938

Predictors of depression and life satisfaction among spousal caregivers in hospice: application of a stress process model.

William E Haley1, Laurie A LaMonde, Beth Han, Allison M Burton, Ronald Schonwetter.   

Abstract

Using a stress process model, risk factors (caregiving stressors, caregiver health, and negative social interactions) and protective factors (caregiving appraisals and social resources) were examined as predictors of family caregiver well-being (depression and life satisfaction). Eighty spousal caregivers of hospice patients with dementia or lung cancer completed structured interviews and self-report measures assessing components of the stress process model. Results suggest that objective measures of patient impairment or amount of care provided are not strong predictors of caregiver depression or life satisfaction. Female gender, caregiver health problems, and negative social interactions were risk factors for poorer caregiver well-being. Caregivers who subjectively appraised caregiving tasks as less stressful, who found meaning and subjective benefits from caregiving, and with more social resources had lower depression and higher life satisfaction, even after controlling for patient impairment and caregiver appraisal variables. Regression models accounted for 42% of variance in caregiver depression and 52% of variance in caregiver life satisfaction. Counseling for hospice family caregivers could utilize the stress process framework, and pay particular attention to finding meaning or subjective benefits from caregiving, and remaining active in social roles. Further research providing evidence on caregiver risk and protective factors could improve the conceptual and empirical basis for psychosocial interventions for hospice family caregivers.

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Mesh:

Year:  2003        PMID: 12854938     DOI: 10.1089/109662103764978461

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  60 in total

1.  Family care and burden at the end of life.

Authors:  Steven H Zarit
Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262

2.  Examining clinically relevant levels of depressive symptoms in mothers following a diagnosis of epilepsy in their children: a prospective analysis.

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3.  [Predictors of personal growth among caregivers of dementia patients].

Authors:  B Leipold; C Schacke; S Zank
Journal:  Z Gerontol Geriatr       Date:  2006-06       Impact factor: 1.281

4.  Family caregiving and emotional strain: associations with quality of life in a large national sample of middle-aged and older adults.

Authors:  David L Roth; Martinique Perkins; Virginia G Wadley; Ella M Temple; William E Haley
Journal:  Qual Life Res       Date:  2009-05-07       Impact factor: 4.147

Review 5.  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

6.  Chronicles of informal caregiving in cancer: using 'The Cancer Family Caregiving Experience' model as an explanatory framework.

Authors:  Z Stamataki; J E Ellis; J Costello; J Fielding; M Burns; A Molassiotis
Journal:  Support Care Cancer       Date:  2013-10-04       Impact factor: 3.603

7.  The relationship between negative life events, psychological distress and life satisfaction: a population-based study.

Authors:  Gunnvor Marum; Jocelyne Clench-Aas; Ragnhild B Nes; Ruth Kjærsti Raanaas
Journal:  Qual Life Res       Date:  2013-09-13       Impact factor: 4.147

8.  Musculoskeletal Discomfort, Physical Demand, and Caregiving Activities in Informal Caregivers.

Authors:  Amy R Darragh; Carolyn M Sommerich; Steven A Lavender; Kelly J Tanner; Kasey Vogel; Marc Campo
Journal:  J Appl Gerontol       Date:  2013-09-09

Review 9.  Application of psychological theories on the role of gender in caregiving to psycho-oncology research.

Authors:  Youngmee Kim; Hannah-Rose Mitchell; Amanda Ting
Journal:  Psychooncology       Date:  2018-12-27       Impact factor: 3.894

10.  The Physical Health of Patients with Advanced Pancreatic Cancer and the Psychological Health of their Family Caregivers When Newly Enrolled in Hospice.

Authors:  Deborah Witt Sherman; Susan C McMillan
Journal:  J Hosp Palliat Nurs       Date:  2015 May-Jun       Impact factor: 1.918

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