A qualitative study, using focused interviews, of the information needs of families whose children's names are on a cerebral palsy register.
BACKGROUND: We were concerned that information held on a register of children with cerebral palsy was not being made available to contributing families, and that the existence and purpose of the register was not sufficiently understood. METHODS: Focused interviews with 13 families selected by purpos...
| Publicado en: | Child: Care, Health & Development Vol. 29; no. 6; pp. 465 - 472 |
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| Autores principales: | , , |
| Formato: | research tables/charts Journal Article |
| Publicado: |
Wiley-Blackwell
Nov2003
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| Acceso en línea: | Ver este registro en EBSCOhost |