Quality of life of children with CP: Condition-specific instrument and proxy reports

Developmental Medicine and Child Neurology

Volumn 50, Issue 3, 2008, Pages 167-

  Davis, Elise ^a   Waters, Elizabeth ^a   Mackinnon, Andrew ^a   Reddihough, Dinah ^a   Boyd, Roslyn ^a   Graham, H Kerr ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CEREBRAL PALSY; CHILD; CLINICAL ASSESSMENT TOOL; COGNITIVE DEFECT; CUSTODY; DAILY LIFE ACTIVITY; EMOTIONALITY; HEALTH CARE ACCESS; HEALTH STATUS; HUMAN; MENTAL DEVELOPMENT; NOTE; PARENTAL BEHAVIOR; PEER GROUP; PERSONAL EXPERIENCE; PRIORITY JOURNAL; PSYCHOLOGICAL WELL BEING; QUALITY OF LIFE; QUALITY OF LIFE INDEX; QUESTIONNAIRE; SELF ESTEEM; SELF REPORT; SOCIAL SUPPORT; SOCIOECONOMICS;

CEREBRAL PALSY; CHILD; FEMALE; HUMANS; MALE; OBSERVER VARIATION; PROXY; QUALITY OF LIFE; QUESTIONNAIRES;

EID: 39649099542     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2008.00167.x     Document Type: Note

References (3)

1. Waters E, Maher E, Salmon L, et al. Development of a condition-specific quality of life scale for children with cerebral palsy: Empirical thematic data reported by parents and children. Child Care Health Dev 2005; 31: 127-35.
2. Davis E, Nicholas C, Waters E, et al. Parent-proxy and child self-reported health-related quality of life: Using qualitative methods to explain the discordance. Qual Life Res 2007; 16: 863-71.
3. Waters E, Davis E, Mackinnon A, et al. Psychometric properties of the quality of life questionnaire for children with C P. Dev Med Child Neurol 2007; 49: 49-55.