Patient explanations for non-attendance at structured diabetes education sessions for newly diagnosed Type 2 diabetes: a qualitative study

Diabet Med. 2015 Jan;32(1):120-8. doi: 10.1111/dme.12556. Epub 2014 Aug 26.

Abstract

Aim: To determine the reasons for non-attendance at structured education sessions among people with a recent diagnosis of Type 2 diabetes.

Methods: This was a qualitative study using semi-structured interviews to elicit the main themes explaining non-attendance. A thematic framework method was applied to analyse the data. People who had not attended structured education were recruited from a population cohort of newly diagnosed Type 2 diabetes from South London (the South London Diabetes cohort study), UK.

Results: A sample of 30 people was interviewed. Three main themes emerged from the qualitative data explaining non-attendance at structured education: (1) lack of information/perceived benefit of the programme (e.g. not being informed about the course by their health professional); (2) unmet personal preferences (e.g. parking, timing); and (3) shame and stigma of diabetes (e.g. not wishing to tell others of diabetes diagnosis).

Conclusion: This is the first time that reasons for non-attendance have been explored in depth among people who have newly diagnosed Type 2 diabetes. Novel reasons identified included non-attendance because of shame and stigma of diabetes. To improve uptake at structured education we need to: consider how health professionals in primary care communicate with their patients on the subject of structured diabetes education; offer alternatives to the traditional group education format; and understand that diabetes is associated with health-related stigma, which may affect participation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cohort Studies
  • Communication Barriers
  • Diabetes Mellitus, Type 2 / psychology*
  • Female
  • Health Knowledge, Attitudes, Practice
  • Humans
  • London / epidemiology
  • Male
  • Middle Aged
  • Patient Acceptance of Health Care
  • Patient Compliance / psychology*
  • Patient Compliance / statistics & numerical data
  • Patient Education as Topic*
  • Pilot Projects
  • Primary Health Care
  • Qualitative Research
  • Self Care
  • Social Perception
  • Social Stigma*
  • Surveys and Questionnaires