Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosis

Education is an essential component of a genetic screening program. Knowledge outcomes were measured after large‐scale workplace education and screening for genetic susceptibility to hereditary hemochromatosis. The aim was to assess knowledge of concepts presented, impact of mode of delivery, and knowledge retention. Education in a group setting was delivered via oral or video presentation and knowledge assessed using self‐administered questionnaires at baseline, 1 month, and 12 months. Over 60% of 11 679 participants correctly answered all questions at baseline, scoring higher with clinical concepts (disease etiology and treatment) than genetic concepts (penetrance and genetic heterogeneity). Revising the education program significantly increased correct responses for etiology (p < 0.002), whilst modifying the knowledge assessment tool significantly increased correct responses for etiology (p < 0.001) and gene penetrance (p < 0.001). For three of the four concepts assessed, use of video was as effective as oral presentation for knowledge outcomes. A significantly higher proportion of those at increased risk of disease (n = 44) responded correctly at 12 months than did controls (n = 82; p = 0.011 for etiology, p = 0.002 for treatment and p = 0.003 for penetrance). Hence, genetic screening can be successfully offered in a group workplace setting, with participants remembering clinical concepts better than genetic concepts up to 1 year later.

[1]  A. Gason,et al.  Tay Sachs disease carrier screening in schools: Educational alternatives and cheekbrush sampling , 2005, Genetics in Medicine.

[2]  R. Williamson,et al.  Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis , 2005, The Lancet.

[3]  M. Aitken,et al.  Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosis , 2004, Clinical genetics.

[4]  A. Gason,et al.  Multimedia messages in genetics: Design, development, and evaluation of a computer-based instructional resource for secondary school students in a Tay Sachs disease carrier screening program , 2004, Genetics in Medicine.

[5]  R. Williamson,et al.  Implementation of HaemScreen, a workplace‐based genetic screening program for hemochromatosis , 2004, Clinical genetics.

[6]  A. Gason,et al.  Evaluation of a Tay‐Sachs Disease screening program , 2003, Clinical genetics.

[7]  K. Barlow-Stewart,et al.  A genetic screening programme for Tay-Sachs disease and cystic fibrosis for Australian Jewish high school students , 2003, Journal of medical genetics.

[8]  Susan Michie,et al.  The multi-dimensional measure of informed choice: a validation study. , 2002, Patient education and counseling.

[9]  R. Williamson,et al.  Assessment of education and counselling offered by a familial colorectal cancer clinic , 2000, Clinical genetics.

[10]  A. Cull,et al.  The use of videotaped information in cancer genetic counselling: a randomized evaluation study. , 1998, British Journal of Cancer.

[11]  M. Richards,et al.  Lay understanding of genetics: a test of a hypothesis. , 1996, Journal of medical genetics.

[12]  C. Scriver,et al.  Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools. , 1996, American journal of human genetics.

[13]  N. Holtzman,et al.  Educating patients about cystic fibrosis carrier screening in a primary care setting. , 1996, Archives of family medicine.

[14]  M. Richards,et al.  Family history and perceived vulnerability to some common diseases: a study of young people and their parents. , 1996, Journal of medical genetics.

[15]  E. Clayton,et al.  Teaching about cystic fibrosis carrier screening by using written and video information. , 1995, American journal of human genetics.

[16]  M. Modell,et al.  The impact of population based screening for carriers of cystic fibrosis. , 1994, Journal of medical genetics.

[17]  S. Loader,et al.  Genetic counseling of asymptomatic carriers in a primary care setting. The effectiveness of screening and counseling for beta-thalassemia trait. , 1986, Annals of internal medicine.

[18]  Norman Crolee Dalkey,et al.  An experimental study of group opinion , 1969 .

[19]  L. Powell,et al.  Haemochromatosis in the new millennium. , 2000, Journal of hepatology.

[20]  L. Furr,et al.  The Genetic Knowledge Index: developing a standard measure of genetic knowledge. , 1999, Genetic testing.

[21]  Patricia Goodson,et al.  The DNA Mystique: The Gene as a Cultural Icon , 1997 .

[22]  M. Kaback,et al.  Tay-Sachs disease: heterozygote screening and prenatal diagnosis--U.S. experience and world perspective. , 1977, Progress in clinical and biological research.