Background:
Melanoma is the most aggressive form of skin cancer, with growing incidence in Ireland. While advances in early detection and treatment have improved survival, the psychological burden following a melanoma diagnosis remains under-recognised. Anxiety, fear of recurrence, and altered body image can significantly impact quality of life. However, limited Irish data exist on the emotional and psychosocial needs of patients following diagnosis.
Aims:
This study aims to explore the psychological impact of melanoma diagnosis among adults treated at the South Infirmary Victoria University Hospital (SIVUH) Dermatology Department. It will assess patients’ emotional responses, coping strategies, perceived support, and satisfaction with communication and care.
Methods:
This cross-sectional, qualitative study will involve semi-structured telephone interviews with a maximum of 25 participants diagnosed with cutaneous melanoma between 2022–2025. Participants will be recruited from existing clinic lists and invited to share their experiences surrounding diagnosis, treatment, and follow-up. Interviews will be audio-recorded, anonymised, and thematically analysed using Braun and Clarke’s six-phase framework to identify key emotional and coping themes.
Expected Outcomes:
The findings will provide insight into the emotional challenges faced by Irish melanoma patients and identify areas where communication, education, or psychosocial support can be strengthened. Results will inform the design of patient-centred interventions and may contribute to improved holistic care pathways for dermatology and oncology services in Ireland.