Literature DB >> 11900237

Lifestyle interference and emotional distress in family caregivers of advanced cancer patients.

Jill I Cameron1, Rene-Louise Franche, Angela M Cheung, Donna E Stewart.   

Abstract

BACKGROUND: Providing end-of-life care at home to a family member with advanced cancer can have a negative impact on the emotional well-being of the family caregiver. The current study examined the impact of providing care on lifestyle and emotional well-being in a sample of caregivers to patients with advanced cancer. The mediation of lifestyle interference between the amount of care provided and emotional distress was specifically examined.
METHODS: Forty-four family caregivers participated in a structured quantitative interview. Lifestyle interference was assessed by the Caregiving Impact Scale, amount of care provided was assessed by the Caregiver Assistance Scale, and emotional distress was assessed by the Profile of Mood States-Short Form. Pearson and partial correlations tested whether lifestyle interference mediated the relationship between caregiving assistance and emotional distress. Regression analyses determined overall correlates of emotional distress.
RESULTS: Three criteria, required to substantiate mediation, were met for total mood disturbance and the depression and tension subscales. An overall regression model identified education level and lifestyle interference to be significant and unique correlates of emotional distress.
CONCLUSIONS: The current results suggest that caregivers experience increased emotional distress, regardless of the amount of care provided, when limited in their ability to participate in valued activities and interests. In addition, caregivers with less than a high school education experience more emotional distress. Therefore, helping caregivers maintain valued aspects of their lifestyle should be an important element of home care.

Entities:  

Mesh:

Year:  2002        PMID: 11900237     DOI: 10.1002/cncr.10212

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


  67 in total

1.  Work productivity and health of informal caregivers of persons with advanced cancer.

Authors:  Susan R Mazanec; Barbara J Daly; Sara L Douglas; Amy R Lipson
Journal:  Res Nurs Health       Date:  2011-09-23       Impact factor: 2.228

Review 2.  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

3.  Update on the family strain questionnaire: a tool for the general screening of caregiving-related problems.

Authors:  Silvia Rossi Ferrario; Paola Baiardi; Anna Maria Zotti
Journal:  Qual Life Res       Date:  2004-10       Impact factor: 4.147

4.  Korean version of the caregiver quality of life index-cancer (CQOLC-K).

Authors:  Young Sun Rhee; Dong Ok Shin; Kwang Mi Lee; Han Jin Yu; Joung Wha Kim; Soon Ok Kim; Ran Lee; Yeon Ok Lee; Nam Shin Kim; Young Ho Yun
Journal:  Qual Life Res       Date:  2005-04       Impact factor: 4.147

5.  Hospice at home service: the carer's perspective.

Authors:  Dorry McLaughlin; Kate Sullivan; Felicity Hasson
Journal:  Support Care Cancer       Date:  2006-08-30       Impact factor: 3.603

6.  When chemotherapy fails: Emotionally charged experiences faced by family caregivers of patients with advanced cancer.

Authors:  Rachel A Rodenbach; Sally A Norton; Marsha N Wittink; Supriya Mohile; Holly G Prigerson; Paul R Duberstein; Ronald M Epstein
Journal:  Patient Educ Couns       Date:  2018-12-12

7.  Confirmatory and exploratory factor analysis of the caregiver quality of life index-cancer with Turkish samples.

Authors:  Zeynep C Ozer; Mehmet Z Firat; Hicran A Bektas
Journal:  Qual Life Res       Date:  2009-06-25       Impact factor: 4.147

8.  Emotional and physical health of informal caregivers of residents at the end of life: the role of social support.

Authors:  Sharon Wallace Williams; Christianna S Williams; Sheryl Zimmerman; Jean Munn; Debra Dobbs; Philip D Sloane
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2008-05       Impact factor: 4.077

9.  Activity restriction and depression in medical patients and their caregivers: a meta-analysis.

Authors:  Brent T Mausbach; Elizabeth A Chattillion; Raeanne C Moore; Susan K Roepke; Colin A Depp; Scott Roesch
Journal:  Clin Psychol Rev       Date:  2011-04-28

10.  Caregivers of patients with cancer fatigue: a high level of symptom burden.

Authors:  Matthew M Clark; Pamela J Atherton; Maria I Lapid; Sarah M Rausch; Marlene H Frost; Andrea L Cheville; Jean M Hanson; Yolanda I Garces; Paul D Brown; Jeff A Sloan; Jarrett W Richardson; Katherine M Piderman; Teresa A Rummans
Journal:  Am J Hosp Palliat Care       Date:  2013-02-21       Impact factor: 2.500

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