Literature DB >> 17624814

The effects of response bias on self-reported quality of life among childhood cancer survivors.

Tara E O'Leary1, Lisa Diller, Christopher J Recklitis.   

Abstract

BACKGROUND: Several studies of long-term adjustment in childhood cancer survivors (CCS) report very positive outcomes, while other studies find significant adjustment problems. These inconsistencies have prompted some investigators to suggest survivors may be biased responders, prone to underreporting on self-report measures. This study tested the hypothesis that CCS are elevated on self-deception response bias (SDRB), and that SDRB is associated with higher ratings of quality-of-life (QOL).
METHODS: One hundred and seven adult (mean age = 31.85) survivors of childhood cancers completed a demographic questionnaire, Short Form-12 (SF-12), Functional Assessment of Cancer Therapy-General (FACT-G), and Self-Deception Enhancement scale (SDE), an SDRB measure.
RESULTS: Survivors' QOL scores were similar to normative groups, but they evidenced much higher levels of response bias. SDE scores were significantly correlated with the FACT-G, and SF-12 Mental Health (but not Physical Health) scores even after accounting for demographic and treatment-related variables.
CONCLUSIONS: CCS show a biased response style, indicating a systematic tendency to deny difficulties on QOL measures. This may complicate QOL studies by inflating survivors' reports of their socio-emotional functioning. Understanding how response bias develops may help us learn more about cancer survivors' adaptation to illness, and the effects of the illness experience on their perceptions of QOL.

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Year:  2007        PMID: 17624814     DOI: 10.1007/s11136-007-9231-3

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  60 in total

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3.  Educational achievement, employment and living situation in long-term young adult survivors of childhood cancer in the Netherlands.

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4.  The late psychosocial consequences of childhood cancer.

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5.  Comparison of psychologic outcome in adult survivors of childhood acute lymphoblastic leukemia versus sibling controls: a cooperative Children's Cancer Group and National Institutes of Health study.

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6.  Posttrauma symptoms in childhood leukemia survivors and their parents.

Authors:  M L Stuber; D A Christakis; B Houskamp; A E Kazak
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7.  Use of the Zung Self-Rating Depression Scale in cancer patients: feasibility as a screening tool.

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9.  Health status of adult long-term survivors of childhood cancer: a report from the Childhood Cancer Survivor Study.

Authors:  Melissa M Hudson; Ann C Mertens; Yutaka Yasui; Wendy Hobbie; Hegang Chen; James G Gurney; Mark Yeazel; Christopher J Recklitis; Neyssa Marina; Leslie R Robison; Kevin C Oeffinger
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10.  High levels of untreated distress and fatigue in cancer patients.

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  28 in total

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3.  Work engagement among breast cancer survivors and the referents: the importance of optimism and social resources at work.

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5.  Measuring quality of life with fuzzy numbers: in the perspectives of reliability, validity, measurement invariance, and feasibility.

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Journal:  Qual Life Res       Date:  2014-10-14       Impact factor: 4.147

6.  Health-Related Quality of Life of Young Adult Survivors of Childhood Cancer: A Review of Qualitative Studies.

Authors:  Chandylen L Nightingale; Gwendolyn P Quinn; Elizabeth A Shenkman; Barbara A Curbow; Bradley J Zebrack; Kevin R Krull; I-Chan Huang
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7.  The Pediatric Toronto Extremity Salvage Score (pTESS): Validation of a Self-reported Functional Outcomes Tool for Children with Extremity Tumors.

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8.  The impact of childhood cancer: Perceptions of adult survivors.

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9.  The utility of parent report in the assessment of working memory among childhood brain tumor survivors.

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10.  Symptom cluster experience profiles in adult survivors of childhood cancers.

Authors:  Lorna Finnegan; Richard T Campbell; Carol Estwing Ferrans; JoEllen Wilbur; Diana J Wilkie; Joan Shaver
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