Open AccessInformed choice in bowel cancer screening: a qualitative study to explore how adults with lower education use decision aids
Author(s) -
Smith Sian K,
Kearney Paul,
Trevena Lyndal,
Barratt Alexandra,
Nutbeam Don,
McCaffery Kirsten J
Publication year - 2014
Publication title -
health expectations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.314
H-Index - 74
eISSN - 1369-7625
pISSN - 1369-6513
DOI - 10.1111/j.1369-7625.2012.00780.x
Subject(s) - decision aids , numeracy , cancer screening , health literacy , patient participation , medicine , qualitative research , informed consent , health care , family medicine , psychology , literacy , directive , medical education , alternative medicine , cancer , computer science , pedagogy , social science , pathology , sociology , programming language , economics , economic growth
Background Offering informed choice in screening is increasingly advocated, but little is known about how evidence‐based information about the benefits and harms of screening influences understanding and participation in screening. Objective We aimed to explore how a bowel cancer screening decision aid influenced decision making and screening behaviour among adults with lower education and literacy. Methods Twenty‐one men and women aged 55–64 years with lower education levels were interviewed about using a decision aid to make their screening decision. Participants were purposively selected to include those who had and had not made an informed choice. Results Understanding the purpose of the decision aid was an important factor in whether participants made an informed choice about screening. Participants varied in how they understood and integrated quantitative risk information about the benefits and harms of screening into their decision making; some read it carefully and used it to justify their screening decision, whereas others dismissed it because they were sceptical of it or lacked confidence in their own numeracy ability. Participants’ prior knowledge and beliefs about screening influenced how they made sense of the information. Discussion and conclusions Participants valued information that offered them a choice in a non‐directive way, but were concerned that it would deter people from screening. Healthcare providers need to be aware that people respond to screening information in diverse ways involving a range of literacy skills and cognitive processes.