Experience of skin disease and relationships with healthcare providers: a qualitative study of Traveller women in Ireland

Abstract

Background

Significant health disparities exist between members of the Travelling community and that of the general population. Barriers to Traveller engagement with health services include the experience or perception of discrimination, cultural and health literacy barriers. Experience of skin disease and interactions with healthcare providers has not been widely explored among this ethnic minority. The formation of positive relationships between the Travelling community and healthcare providers is important in the promotion of treatment adherence and improving health outcomes.

Objectives

We aimed to investigate Travellers' experience of skin disease and their relationships with healthcare providers.

Methods

Focus groups were conducted with a purposive sample of female members of the Irish Travelling community with experience of skin health issues, between January 2018 and April 2018. Three focus groups were conducted at three separate locations with ten participants in each group. Themes were identified from the focus group transcripts using an inductive thematic analysis framework.

Results

Emergent themes surrounding relationships between Travellers and healthcare providers included health literacy, discrimination, information inconsistency, trust and communication. Factors that were valued in the creation of positive relationships included an appreciation of varying degrees of health literacy, the provision of sufficient information tailored to an individual's needs and a demonstration of cultural competence.

Conclusion

Dermatologists are well placed to provide practical, customised, treatment guidance and engage patients while integrating their culturally based beliefs.

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