Affiliation:
1. Department of Medical Genetics, Faculty of Medicine University of British Columbia Vancouver British Columbia Canada
2. BC Children's Hospital Research Institute Vancouver British Columbia Canada
3. BC Women's Hospital Research Institute Vancouver British Columbia Canada
Abstract
AbstractIntroductionPrevious research has demonstrated that children lacking knowledge about genetic disorders may have harmful attitudes toward people with disabilities, but disability awareness can successfully modify these attitudes. We explored adolescents' implicit and explicit attitudes toward peers with genetic conditions to determine whether improved genetics/genomics literacy can mitigate the impact of ableism in this population.MethodsEnglish‐speaking adolescents (10–18 years) from British Columbia were invited to complete a Disability Attitudes Implicit Association Test (DA‐IAT) and participate in a semi‐structured focus group centering on a fictionalized vignette about an adolescent with Down syndrome. We used pragmatism as an analytical paradigm. Descriptive and inferential statistics were used to analyze DA‐IAT and sociodemographic data; phronetic iterative analysis with constant comparison as a coding strategy for transcripts; and interpretive description to develop a conceptual model.ResultsTwenty‐two adolescents completed the DA‐IAT and participated in one of four focus groups. Participants had a statistically significant implicit preference for non‐disabled people (D‐score = 0.72, SD = 0.44; t = 7.18, p < .00001). They demonstrated greater diversity in their explicit attitudes during the focus groups. Although participants articulated a positive attitude toward improved genetics education, results demonstrate their belief that social and personal interactions with disabled peers would be essential to address negative perceptions.ConclusionsThis study lays important groundwork to understand, explain, and influence the negative attitudes of adolescents toward individuals with disabilities. Findings will be used to inform the design of interventions that address biased perceptions of people with genetic disorders, with the goal of reducing prejudices and improving social interactions.