Living with bipolar disorder – stigma, barriers and facilitators of care
The aim of the study is to explore the impact of stigma and discrimination experiences on treatment seeking and care for people living with bipolar disorder. This questionnaire will include questions about discrimination, stigma and self-stigma. It will also gather information about other features that may improve access to care, such as coping style, self-care strategies and social support.
surveyswesternsydney.au1.qualtrics.com/jfe/form/SV_1RYvA9h9JnmVRcy
Articles are available to read for free via Open Access:
Perich, T., Kakakios, K., & Fraser, I. (2024). Telehealth-delivered recovery-orientated well-being plan group program for bipolar disorder: a pilot randomised feasibility and acceptability study. Behavioural and Cognitive Psychotherapy, 52(6), 681–686. doi:10.1017/S1352465824000316
Perich, T., Kakakios, K., & Fraser, I. (2023). ‘I almost felt like I can be a little bit more honest’: experiences of a telehealth group for bipolar disorder. The Cognitive Behaviour Therapist, 16, e26. doi:10.1017/S1754
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