Further validation of the parent experience of child illness scale

被引：15

作者：

Bonner, Melanie J. ^{[1
,2
,3
]}

Hardy, Kristina K. ^{[1
,2
]}

Willard, Victoria W. ^{[3
]}

Hutchinson, Katherine C. ^{[3
]}

Guill, A. Bebe ^{[2
]}

机构：

[1] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA

[2] Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Durham, NC 27710 USA

[3] Duke Univ, Dept Psychol & Neurosci, Durham, NC 27710 USA

来源：

CHILDRENS HEALTH CARE | 2008年 / 37卷 / 02期

关键词：

D O I：

10.1080/02739610802006569

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

The objective of this research is to provide further validation of the Parent Experience of Child Illness (PECI) scale. One hundred twenty-five caregivers of patients (age <1-17 years) diagnosed with cancer returned questionnaire data at Time 1, and 75 caregivers at Time 2. Findings provide support for the psychometric properties of the PECI, including good test-retest reliability and convergent and discriminant validity. The PECI appears to be a valid assessment tool for evaluation of the distress and perceived resources of caregivers of pediatric cancer patients. Continued evaluation is needed with other chronic illness groups.

引用

页码：145 / 157

页数：13

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