“…Young patients, those with Crohn's disease and those with a first-degree relative with IBD also scored relatively highly, as patients did when the questionnaire developed by Jones et al was applied in clinical practice [5]. By contrast, the authors found no association between knowledge and either disease duration or quality of life and it is clear from other studies that, while education may be desirable from both the patients' and the healthcare professionals' viewpoint, knowledge itself does not necessarily translate into improved overall wellbeing [2,20,21]. The increasing use of IBD registries and databases has placed emphasis on collating large volumes of biological, psychological and socioeconomic data from patients [22,23] and such projects require validated and concise questionnaires to acquire reliable results.…”