Literature DB >> 27472189

Benefit Finding and Quality of Life in Caregivers of Childhood Cancer Survivors: The Moderating Roles of Demographic and Psychosocial Factors.

Molly H Gardner1, Sylvie Mrug, David C Schwebel, Sean Phipps, Kimberly Whelan, Avi Madan-Swain.   

Abstract

BACKGROUND: Benefit finding, or finding positive outcomes in the face of adversity, may play a role in predicting quality of life (QoL) among caregivers, but mixed results suggest that other factors may moderate this relationship.
OBJECTIVE: This study examined demographic and psychosocial moderators of the association between benefit finding and QoL among caregivers of childhood cancer survivors.
METHODS: Caregivers of childhood cancer survivors (n = 83) completed measures of benefit finding, QoL, coping, optimism, social support, caregiving demand, posttraumatic stress, and demographics.
RESULTS: The relationship between benefit finding and QoL was moderated by caregiver age, marital status, socioeconomic status, geographic location, acceptance and emotion-focused coping, optimism, caregiving demand, and posttraumatic stress. Benefit finding was more strongly related to QoL among caregivers with fewer demographic/psychosocial resources.
CONCLUSIONS: Results suggest that finding benefits in the cancer experience may have a greater positive impact for caregivers with relatively fewer demographic and psychosocial resources and may have less of an impact for caregivers with relatively greater resources. Findings further point to the complex nature of QoL among caregivers of childhood cancer survivors. IMPLICATIONS FOR PRACTICE: Results may aid clinicians in identifying caregivers at particular risk for low QoL. They may be counseled to find benefits in their experience or provided with resources to strengthen other factors that impact QoL.

Entities:  

Mesh:

Year:  2017        PMID: 27472189      PMCID: PMC5274609          DOI: 10.1097/NCC.0000000000000419

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  48 in total

1.  The World Health Organization's WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. A report from the WHOQOL group.

Authors:  S M Skevington; M Lotfy; K A O'Connell
Journal:  Qual Life Res       Date:  2004-03       Impact factor: 4.147

2.  Quality of life among parents of children with cancer or brain tumors: the impact of child characteristics and parental psychosocial factors.

Authors:  Kristin Litzelman; Kris Catrine; Ronald Gangnon; Whitney P Witt
Journal:  Qual Life Res       Date:  2011-02-02       Impact factor: 4.147

3.  Long term posttraumatic growth after breast cancer: prevalence, predictors and relationships with psychological health.

Authors:  S Lelorain; A Bonnaud-Antignac; A Florin
Journal:  J Clin Psychol Med Settings       Date:  2010-03

4.  Health-related quality of life of mothers of children with leukemia in Japan.

Authors:  Shin Yamazaki; Shigeru Sokejima; Tetsuya Mizoue; Akira Eboshida; Shunichi Fukuhara
Journal:  Qual Life Res       Date:  2005-05       Impact factor: 4.147

5.  Assessing coping strategies: a theoretically based approach.

Authors:  C S Carver; M F Scheier; J K Weintraub
Journal:  J Pers Soc Psychol       Date:  1989-02

6.  Posttraumatic growth in adolescent survivors of cancer and their mothers and fathers.

Authors:  Lamia P Barakat; Melissa A Alderfer; Anne E Kazak
Journal:  J Pediatr Psychol       Date:  2005-08-10

7.  Psychosocial and demographic predictors of quality of life in a large sample of cancer patients.

Authors:  Patricia A Parker; Walter F Baile; Carl de de Moor; Lorenzo Cohen
Journal:  Psychooncology       Date:  2003-03       Impact factor: 3.894

8.  Benefit finding in fathers of childhood cancer survivors: a retrospective pilot study.

Authors:  Molly A Hensler; Ernest R Katz; Lori Wiener; Roger Berkow; Avi Madan-Swain
Journal:  J Pediatr Oncol Nurs       Date:  2013 May-Jun       Impact factor: 1.636

9.  Caregiving, single parents and cumulative stresses when caring for a child with cancer.

Authors:  L Granek; Z R S Rosenberg-Yunger; D Dix; R J Klaassen; L Sung; J Cairney; A F Klassen
Journal:  Child Care Health Dev       Date:  2012-11-02       Impact factor: 2.508

10.  Building Bridges From Hospital to Home: Understanding the Transition Experience for the Newly Diagnosed Pediatric Oncology Patient.

Authors:  Patricia A Branowicki; Judith A Vessey; Kendal L Jackson Temple; Amanda J Lulloff
Journal:  J Pediatr Oncol Nurs       Date:  2015-12-14       Impact factor: 1.636

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  5 in total

1.  Meaning Making and Religious Engagement Among Survivors of Childhood Brain Tumors and Their Caregivers.

Authors:  Em Rabelais; Nora L Jones; Connie M Ulrich; Janet A Deatrick
Journal:  Oncol Nurs Forum       Date:  2019-03-01       Impact factor: 2.172

2.  Exploring the Moderating Role of Benefit Finding on the Relationship Between Child Problematic Behaviours and Psychological Distress in Caregivers of Children with ASD.

Authors:  Brian Lovell; Mark A Wetherell
Journal:  J Autism Dev Disord       Date:  2020-02

3.  Quality of Life in Family Caregivers of Adolescents with Depression in China: A Mixed-Method Study.

Authors:  Yinying Zhang; Min Yang; Xin Guo; Qiongni Chen
Journal:  Patient Prefer Adherence       Date:  2020-07-30       Impact factor: 2.711

4.  Estimating cancer treatment intensity from SEER cancer registry data: methods and implications for population-based registry studies of pediatric cancers.

Authors:  Jessica L Tobin; Stefanie M Thomas; David R Freyer; Ann S Hamilton; Joel E Milam
Journal:  Cancer Causes Control       Date:  2020-08-05       Impact factor: 2.532

5.  Health behaviors of caregivers of childhood cancer survivors: a cross-sectional study.

Authors:  In Young Cho; Nack-Gyun Chung; Hee Jo Baek; Ji Won Lee; Ki Woong Sung; Dong Wook Shin; Jung Eun Yoo; Yun-Mi Song
Journal:  BMC Cancer       Date:  2020-04-07       Impact factor: 4.430

  5 in total

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