REFERENCES
- Anderson R. The Aftermath of Stroke: The Experience of Patients and their Families. New York: Cambridge University Press; 1992.
- Forster A, Smith J, Young J, Knapp P, House A, Wright J. Information provision for stroke patients and their caregivers. Cochrane Database Syst Rev. 2001;2.
- Wellwood I, Denis MS, Warlow CP. Perceptions and knowledge of stroke among surviving patients with stroke and their carers. Age Ageing. 1994;23:293–298.
- Rodgers H, Bond S, Curless R. Inadequacies in the provision of information to stroke patients and their families. Age Ageing. 2001;30:129–133.
- Mold F, McKevitt C, Wolfe C. A review and commentary of the social factors which influence stroke care: issues of inequality in qualitative literature. Health Soc Care Community. 2003;11:405–414.
- O'Mahony PG, Rodgers H, Thomson RG, Dobson R, James OFW. Satisfaction with information and advice received by stroke patients. Clin Rehabil. 1997;11:68–72.
- Wiles R, Pain H, Buckland S, McLellan L. Providing appropriate information to patients and carers following a stroke. I Adv Nurs. 1998;28:794–801.
- Rodgers H, Atkinson C, Bond S, Suddes M, Dobson R, Curless R. Randomized controlled trial of a comprehensive stroke education program for patients and caregivers. Stroke. 1999;30:2585–2591.
- World Health Organization. A Declaration on the Promotion of Patients' Rights in Europe. Amsterdam: Author; 1994.
- Hanger HC, Walker G, Paterson LA, McBride S, Sainsbury R. What do patients and their carers want to know about stroke? A two year followup study. Clin Rehabil. 1998;12:45–52.
- Eames S, McKenna K, Worrall L, Read S. Grand rounds. The suitability of written education materials for stroke survivors and their carers. Top Stroke Rehabil. 2003;10:70–83.
- Wellwood I, Denis MS, Warlow CP. Patients' and carers' satisfaction with acute stroke management. Age Ageing. 1995;24:519–524.
- Audit Commission. What Seems To Be The Matter: Communication Between Hospitals and Patients. London: Her Majesty's Stationary Office; 1993. Cited by Wiles R, Pain H, Buckland S, McLellan L. Providing appropriate information to patients and carers following a stroke. I Adv Nurs. 1998;28: 794–801.
- Parr S, Byng S, Gilpin S, Ireland C. Talking about Aphasia: Living with Loss of Language after Stroke. Bristol, Pennsylvania: Open University Press; 1997.
- Stirling A. "Communication Ramps" for People with Severe Acquired Language Disability. Merseyside Health Action Zone Fellowship Report. United Kingdom: Merseyside Health Action Zone; 2003.
- World Health Organization. International Classification of Functioning, Disability and Health. Geneva: Author; 2001.
- Jordan L, Kaiser W. Aphasia a Social Aapproach. London: Chapman and Hall; 1996.
- Patton MQ. Qualitative Research and Evaluation Methods. 3rd ed. Thousand Oaks, California: Sage Publications; 2002.
- Kagan AK, Kimelman DZ. Informed consent in aphasia research: myth or reality? Clin Aphasiol. 1995;23:65–75.
- Crombie IK, Davies HTO. Research in Health Care: Design, Conduct and Interpretation of Health Services Researchl. Chichester, New York: Wiley; 1996.
- Spradley JP. Participant Observation. Victoria: Thomas Learning Inc; 1980.
- Worrall L, McCooey R, Davidson B, Larkins B, Hickson L. The validity of functional assessments of communication and the activity/participation components of the ICIDH-2: do they reflect what really happens in real-life? I Commun Disord. 2002; 35:213–216.
- O'Connell B, Baker L, Prosser A. The educational needs of caregivers of stroke survivors in acute and community settings.J Neurosci Nurs. 2003;35:21–28.
- Avis M. Incorporating patients' voices in the audit process. Qual Health Care. 1997;6:86–91.
- Miles MB. Qualitative Data Analysis: An Expanded Sourcebook. 2nd ed. Thousand Oaks, California: Sage Publications; 1994.
- Urden LD. Patient satisfaction measurement: current issues and implications. Outcomes Manage. 2002;6:125–131
- Duxbury J. Difficult Patients. Oxford, Boston: Butterworth-Heinemann; 2000.
- Stockwell F. The Unpopular Patient. London: Croom Helm; 1994.
- Finlay L. Good patients and bad patients: how occupational therapists view their patients/clients. Br Occup Ther. 1997;60:440–446.
- Waterworth S, Luker KA. Reluctant collaborators: Do patients want to be involved in decisions concerning care?J Adv Nurs. 1990;15:971-976.
- Johnson A, Sandford J, Tyndall J. Written and verbal information versus verbal information only for patients being discharged from acute hospital settings to home. Cochrane Database Syst Rev. 2003;4.