Using the Internet for information about breast cancer: a questionnaire-based study

Patient Educ Couns. 2013 Sep;92(3):413-7. doi: 10.1016/j.pec.2013.06.018. Epub 2013 Jul 23.

Abstract

Objectives: To identify the proportion of breast cancer patients that used the Internet for breast cancer information; to classify patterns of use based on patient demographics; and to evaluate whether using the Internet for this purpose was beneficial or problematic. Also to recognize whether a specific demographic group was more likely to experience problems when using the Internet for breast cancer information.

Methods: A 10-item questionnaire was given to patients who attended the breast unit at the University Hospital of South Manchester between May and June 2011 following breast cancer treatment within the last 5 years.

Results: 200 questionnaires were completed. 50.5% of patients had used the Internet for breast cancer information, with younger (p<0.001) patients with a higher household income (p<0.001) being most likely to do so. The majority (73%) found it beneficial; however 31% had experienced problems. Ethnicity affected the likelihood of experiencing problems with white patients encountering fewer problems (25%) than non-white patients (64%) (p=0.008).

Conclusion: A significant proportion of breast cancer patients will encounter difficulties when using the Internet for breast cancer information, particularly those from ethnic minorities.

Practice implications: Health professionals need to include a discussion about Internet use in consultations with breast cancer patients.

Keywords: Breast cancer; Ethnic minorities; Health inequalities; Internet use.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Attitude to Computers
  • Breast Neoplasms / ethnology
  • Breast Neoplasms / psychology*
  • Ethnicity / statistics & numerical data*
  • Female
  • Health Status Disparities
  • Humans
  • Internet / statistics & numerical data*
  • Middle Aged
  • Patient Education as Topic / methods*
  • Patient Education as Topic / standards
  • Pilot Projects
  • Socioeconomic Factors
  • Surveys and Questionnaires
  • United Kingdom
  • Young Adult