Literature DB >> 17876187

Self-perceived burden in cancer patients: validation of the Self-perceived Burden Scale.

Leigh Ann Simmons1.   

Abstract

Although caregiver burden has been studied extensively, cancer patients' self-perceived burden on caregivers has been an understudied phenomenon. The purpose of this cross-sectional study was to validate the Self-perceived Burden Scale, a 10-item self-report instrument designed to measure chronically ill patients' experience of burden. Participants were 106 cancer patients (site nonspecific) receiving active cancer treatments at a university cancer center. Factor analysis results indicated that a 9-item version of the scale consisted of a single factor and had good reliability (alpha = .938). Convergent validity was demonstrated with global quality of life (r = -0.546, P < .001), physical well-being (r = -0.547, P < .001), emotional well-being (r = -0.549, P < .001), functional well-being (r = -0.404, P < .001), financial satisfaction (r = -0.284, P = .001), and depression (r = 0.414, P <.001). Tests of divergent validity indicated that the Self-perceived Burden Scale was independent of age, number of people living in the household, disease site, cancer treatment, and sociofamilial well-being. Findings indicate that the Self-perceived Burden Scale may be a useful instrument to assess patients' perceptions of burden on their caregivers. Further studies of the role of patient burden in psychosocial well-being and global quality of life, including validation of the Self-perceived Burden Scale on a larger study sample, are warranted.

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Year:  2007        PMID: 17876187     DOI: 10.1097/01.NCC.0000290816.37442.af

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


  19 in total

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Review 3.  Assessing the social impact of cancer: a review of available tools.

Authors:  Barbara Muzzatti; M Antonietta Annunziata
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4.  Trajectory and predictors of quality of life during the dying process: roles of perceived sense of burden to others and posttraumatic growth.

Authors:  Siew Tzuh Tang; Wen-Cheng Chang; Jen-Shi Chen; Po-Jung Su; Chia-Hsun Hsieh; Wen-Chi Chou
Journal:  Support Care Cancer       Date:  2014-05-28       Impact factor: 3.603

5.  Are survivors who report cancer-related financial problems more likely to forgo or delay medical care?

Authors:  Erin E Kent; Laura P Forsythe; K Robin Yabroff; Kathryn E Weaver; Janet S de Moor; Juan L Rodriguez; Julia H Rowland
Journal:  Cancer       Date:  2013-07-31       Impact factor: 6.860

6.  Economic and objective burden of caregiving on informal caregivers of patients with systemic vasculitis.

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7.  Perspectives on the Delirium Experience and Its Burden: Common Themes Among Older Patients, Their Family Caregivers, and Nurses.

Authors:  Eva M Schmitt; Jacqueline Gallagher; Asha Albuquerque; Patricia Tabloski; Hyo Jung Lee; Lauren Gleason; Lauren S Weiner; Edward R Marcantonio; Richard N Jones; Sharon K Inouye; Dena Schulman-Green
Journal:  Gerontologist       Date:  2019-03-14

8.  Dealing with the lack of evidence to treat depression in older patients with cancer: French Societies of Geriatric Oncology (SOFOG) and PsychoOncology (SFFPO) position paper based on a systematic review.

Authors:  Bérengère Beauplet; Ophélie Soulie; Jean-Yves Niemier; Cécile Pons-Peyneau; Drifa Belhadi; Camille Couffignal; Virginie Fossey-Diaz
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9.  Self-perceived burden and influencing factors in patients with cervical cancer administered with radiotherapy.

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Journal:  World J Clin Cases       Date:  2021-06-16       Impact factor: 1.337

10.  Medical Assistance in Dying in patients with advanced cancer and their caregivers: a mixed methods longitudinal study protocol.

Authors:  Madeline Li; Gilla K Shapiro; Roberta Klein; Anne Barbeau; Anne Rydall; Jennifer A H Bell; Rinat Nissim; Sarah Hales; Camilla Zimmermann; Rebecca K S Wong; Gary Rodin
Journal:  BMC Palliat Care       Date:  2021-07-21       Impact factor: 3.234

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