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Psychology, Health & Medicine Volume 1, 1996 - Issue 3
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Original Articles

The effects of different kinds of information on women attending an out-patient breast clinic

S. Michie Health Psychology Unit,
,
C. Rosebert Health Psychology Unit,
,
J. Heaversedge Health Psychology Unit,
,
S. Madden Health Psychology Unit,
&
S. Parbhoo Department of Surgery, Royal Free Hospital School of Medicine, London, UK
Pages 285-296 | Published online: 24 Oct 2007

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Aaron Smith-McLallen, Martin Fishbein & RobertC. Hornik. (2011) Psychosocial Determinants of Cancer-Related Information Seeking Among Cancer Patients. Journal of Health Communication 16:2, pages 212-225.
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Z Chouliara, K G Power, V Swanson & F Johnstone. (2002) Factors associated with breast screening attendance: A controlled comparison between attenders and non-attenders in Scotland. International Journal of Health Promotion and Education 40:3, pages 78-90.
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P. Ley. (1998) The use and improvement of written communication in mental health care and promotion. Psychology, Health & Medicine 3:1, pages 19-53.
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L. Sherr. (1998) Health promotion and mental illness—an overview. Psychology, Health & Medicine 3:1, pages 5-18.
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Articles from other publishers (28)

Patricia Estefania Ayala Aguirre, Melina Martins Coelho, Daniela Rios, Maria Aparecida Andrade Moreira Machado, Agnes Fátima Pereira Cruvinel & Thiago Cruvinel. (2017) Evaluating the Dental Caries-Related Information on Brazilian Websites: Qualitative Study. Journal of Medical Internet Research 19:12, pages e415.
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Jennifer K. Bernat, Ted A. Skolarus, Sarah T. Hawley, David A. Haggstrom, May Darwish-Yassine & Daniela A. Wittmann. (2016) Negative information-seeking experiences of long-term prostate cancer survivors. Journal of Cancer Survivorship 10:6, pages 1089-1095.
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Jennifer K. Bernat, Daniela A. Wittman, Sarah T. Hawley, Daniel A. Hamstra, Alexander M. Helfand, David A. Haggstrom, May Darwish-Yassine & Ted A. Skolarus. (2016) Symptom burden and information needs in prostate cancer survivors: a case for tailored long-term survivorship care. BJU International 118:3, pages 372-378.
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Jane M. Ussher, Janette Perz & Emilee Gilbert. (2012) Information needs associated with changes to sexual well‐being after breast cancer. Journal of Advanced Nursing 69:2, pages 327-337.
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Orit Cohen Castel, Mordechai Alperin, Lea Ungar, Ina Kravtsov, Gilad E. Amiel & Khaled Karkabi. (2010) Urologists’ Attitudes Regarding Information Sharing with Prostate Cancer Patients—Is There a Common Ground for Collaboration with Family Physicians?. Journal of Cancer Education 26:2, pages 315-321.
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Jui-Chen Huang. 2010. Computational Collective Intelligence. Technologies and Applications. Computational Collective Intelligence. Technologies and Applications 402 410 .
Kristian Pollock, Karen Cox, Penny Howard, Eleanor Wilson & Nima Moghaddam. (2007) Service user experiences of information delivery after a diagnosis of cancer: a qualitative study. Supportive Care in Cancer 16:8, pages 963-973.
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Orit Cohen Castel, Lea Ungar, Mordechai Alperin, Gilad E. Amiel & Khaled Karkabi. (2007) Family physicians’ perceptions, beliefs, and attitudes regarding information sharing with prostate cancer patients throughout the course of the disease. Supportive Care in Cancer 16:8, pages 955-961.
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Jeffrey K. Vallance, Kerry S. CourneyaLorian M. Taylor, Ronald C. Plotnikoff & John R. Mackey. (2006) Development and Evaluation of a Theory-Based Physical Activity Guidebook for Breast Cancer Survivors. Health Education & Behavior 35:2, pages 174-189.
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Kinta Beaver & Gary Witham. (2007) Information needs of the informal carers of women treated for breast cancer. European Journal of Oncology Nursing 11:1, pages 16-25.
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Julie Redfern, Elizabeth Ellis, Tom Briffa & Saul B Freedman. (2006) Development and testing of innovative patient resources for the management of coronary heart disease (CHD): a descriptive study. BMC Health Services Research 6:1.
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Sivia Barnoy, Yoram Bar-Tal & Bracha Zisser. (2006) Correspondence in informational coping styles: How important is it for cancer patients and their spouses?. Personality and Individual Differences 41:1, pages 105-115.
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Daniel R. Longo. (2005) Understanding health information, communication, and information seeking of patients and consumers: a comprehensive and integrated model. Health Expectations 8:3, pages 189-194.
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Yoram Bar-Tal, Sivia Barnoy & Bracha Zisser. (2005) Whose informational needs are considered? A comparison between cancer patients and their spouses’ perceptions of their own and their partners’ knowledge and informational needs. Social Science & Medicine 60:7, pages 1459-1465.
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Charlotte Rees, Reem Abed & Charlotte Sheard. (2003) Development of a reliable and valid questionnaire to test the prostate cancer knowledge of men with the disease. Patient Education and Counseling 51:3, pages 285-292.
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Gbogboade Ademiluyi, Charlotte E Rees & Charlotte E Sheard. (2003) Evaluating the reliability and validity of three tools to assess the quality of health information on the Internet. Patient Education and Counseling 50:2, pages 151-155.
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Gerard Riley, Kim Brown & Catherine Searle. (2003) Are information packs useful in community rehabilitation?. British Journal of Therapy and Rehabilitation 10:3, pages 110-114.
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C.E. Rees, J.E. Ford & C.E. Sheard. (2003) Patient information leaflets for prostate cancer: which leaflets should healthcare professionals recommend?. Patient Education and Counseling 49:3, pages 263-272.
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Charlotte E. Rees, Charlotte E. Sheard & Kezia Echlin. (2003) The relationship between the information-seeking behaviours and information needs of partners of men with prostate cancer: a pilot study. Patient Education and Counseling 49:3, pages 257-261.
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Kezia N. Echlin & Charlotte E. Rees. (2002) Information Needs and Information-seeking Behaviors of Men With Prostate Cancer and Their Partners: A Review of the Literature. Cancer Nursing 25:1, pages 35-41.
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Charlotte E. Rees & Peter A. Bath. (2001) The Use of Between-Methods Triangulation in Cancer Nursing Research. Cancer Nursing 24:2, pages 104-111.
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Charlotte E. Rees & Peter A. Bath. (2000) Mass media sources for breast cancer information: their advantages and disadvantages for women with the disease. Journal of Documentation 56:3, pages 235-249.
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Charlotte E. Rees & Peter A. Bath. (2000) The information needs and source preferences of women with breast cancer and their family members: a review of the literature published between 1988 and 1998. Journal of Advanced Nursing 31:4, pages 833-841.
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Charlotte E. Rees & Peter A. Bath. (2000) Meeting the Information Needs of Adult Daughters of Women With Early Breast Cancer. Cancer Nursing 23:1, pages 71-79.
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Charlotte E. ReesPeter A. BathMichael Lloyd‐Williams. (2002) The information concerns of spouses of women with breast cancer: patients’ and spouses’ perspectives. Journal of Advanced Nursing 28:6, pages 1249-1258.
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C. Davey, J. Austoker & C. Jansen. (2016) Improving written information for women about cervical screening: evidence-based criteria for the content of letters and leaflets. Health Education Journal 57:3, pages 263-281.
Crossref
Susan Michie. 1998. Comprehensive Clinical Psychology. Comprehensive Clinical Psychology 153 169 .
Jonas Poelmans, Gerda Verheyden, Herman Van der Mussele & Guido Dedene. (2013) Stepwise Implementation of a Specialist Breast Nurse Position and Clinical Pathway: Impact on Patient Satisfaction. SSRN Electronic Journal.
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