## Abstract ## BACKGROUND Chemotherapy‐induced nausea and emesis (CINE) is one of the most dreaded side effects of cancer therapy. To investigate the influence of these symptoms on a patient's quality of life (QOL), a validated tool measuring many domains is needed. ## METHODS A QOL questionnair
Psychometric properties of the quality of life questionnaire for children with CP
✍ Scribed by Elizabeth Waters; Elise Davis; Andrew Mackinnon; Roslyn Boyd; H Kerr Graham; Sing Kai Lo; Rory Wolfe; Richard Stevenson; Kristie Bjornson; Eve Blair; Peter Hoare; Ulrike Ravens-Sieberer; Dinah Reddihough
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 137 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0012-1622
No coin nor oath required. For personal study only.
✦ Synopsis
This paper describes the development and psychometric properties of a condition‐specific quality of life instrument for children with cerebral palsy (CP QOL‐Child). A sample of 205 primary caregivers of children with CP aged 4 to 12 years (mean 8y 5mo) and 53 children aged 9 to 12 years completed the CP QOL‐Child. The children (112 males, 93 females) were sampled across Gross Motor Function Classification System (GMFCS) levels (Level I=18%, II=28%, III=14%, IV=11%, V=27%). Primary caregivers also completed other measures of child health (Child Health Questionnaire; CHQ), QOL (KIDSCREEN), and functioning (GMFCS). Internal consistency ranged from 0.74 to 0.92 for primary caregivers and from 0.80 to 0.90 for child self‐report. For primary caregivers, 2‐week test‐retest reliability ranged from 0.76 to 0.89. The validity of the CP QOL is supported by the pattern of correlations between CP QOL‐Child scales with the CHQ, KIDSCREEN, and GMFCS. Preliminary statistics suggest that the child self‐report questionnaire has acceptable psychometric properties. The questionnaire can be freely accessed at http://www.deakin.edu.ac/hmnbs/chase/cerebralpalsy/cp_qol_home.php
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