Chronic Spontaneous Urticaria (CSU) is a recurrent appearance of wheals (hives), with or without swelling, that occurs unpredictably for more than six weeks. CSU is often described as an autoimmune condition with no identifiable trigger. It is therefore difficult to treat and patients can find it hard to get a diagnosis. CSU carries a high disease burden and has an impact on quality of life (QoL) and mental health, however it is a condition that has received little focus in the research literature. A recent review (Donnelly et al., 2023) exploring the psychosocial factors of CSU found just 18 studies, only two of which were qualitative in design. Psychosocial factors found to be related to CSU onset and aggravation included stress, post-traumatic stress, anxiety, OCD and personality characteristics. Symptoms affected lifestyle, sleep, body image, quality of life, levels of depression and anxiety. Qualitative studies reported on frustration with the healthcare service and lack of acknowledgement of the psychological impact of CSU.
This PhD project will explore the psychosocial burden of CSU from the patient and healthcare professional perspective. Very little research has been carried out on this condition in the UK and nothing is known about the experiences of patients with the UK healthcare system. Patients and healthcare professionals treating CSU will be interviewed to explore experiences. A cross-sectional survey will be undertaken to characterise the impact of CSU on QoL in the UK. Finally focus groups will be run to explore ways in which patient pathways can be improved.
This PhD would suit someone with an UG degree in psychology and a post-graduate qualification in health psychology or similar. Experience of research in this field would be desirable but not essential and training will be given.
References
Donnelly, J., Ridge, K., O’Donovan, R. et al. Psychosocial factors and chronic spontaneous urticaria: a systematic review. BMC Psychol 11, 239 (2023). https://doi.org/10.1186/s40359-023-01284-2