Parents’ information needs about the treatment of their chronically ill child: A qualitative study
- 1 August 2006
- journal article
- Published by Elsevier in Patient Education and Counseling
- Vol. 62 (2) , 228-234
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- ‘It takes three to tango’:Social Science & Medicine, 2004
- Parents’ perceptions of the information provided to them about their child's leukaemiaEuropean Journal of Oncology Nursing, 2003
- Parents’ Needs for Knowledge concerning the Medical Diagnosis of their ChildrenJournal of Child Health Care, 2002
- The needs of parents with chronically sick children: a literature reviewJournal of Advanced Nursing, 2001
- Variability in patient preferences for participating in medical decision making: implication for the use of decision support toolsQuality and Safety in Health Care, 2001
- Qualitative research in health care: Analysing qualitative dataBMJ, 2000
- Consulting the `experts': children's and parents' perceptions of psycho-educational interventions in the context of juvenile chronic arthritisHealth Education Research, 1999
- Sharing decisions with patients: is the information good enough?BMJ, 1999
- Preferences for Participation in Treatment Decision Making and Information Needs of Parents of Children With Cancer: A Pilot StudyJournal of Pediatric Oncology Nursing, 1999
- Qualitative Research: Qualitative interviews in medical researchBMJ, 1995