This project is funded by:
There is a research gap in understanding the mental health of individuals with the long term health condition Cystic Fibrosis (CF). Research has indicated that mental health concerns like depression and anxiety are common among people with CF (PWCF), emerging in childhood, and if untreated can have a negative impact on both physical and mental outcomes including lung function, pulmonary exacerbations, BMI and health related quality of life (Bathgate, Hjelm, Filigno, Smith & Georgiopoulous, 2022). Symptoms of depression such as loss of appetite, fatigue, and insomnia, can overlap with CF related symptoms, ensuing further negative health implications. In CF, the prevalence of depression ranges from 29% among children and adolescents, 33% among adults, anxiety in adults has ranged from 30% to 33% (Smith, Modi, Quittner & Wood, 2010; Latchford & Duff, 2013). Research has indicated that care pathways and provision of high-quality care for depression/anxiety should be in place prior to implementation of a screening programme (Quittner et al., 2016). However, psychoeducation resources remain lacking.
This project aims to further mental health research in CF with the following programme of planned research:
1. Umbrella review – a full systematic literature review and an up-to-date synthesis of mental health in CF research.
2. The psychometrics of CF specific measures – by consulting the systematic review to make research informed decisions, the development develop an updated online survey, building on the work of research to date (e.g., McHugh et al., 2023). The project will deliver a survey to explore mental health outcomes and to continue to validate CF specific measures to better understand the mental health experience in PWCF.
3. Scoping for the development of an online intervention/psychoeducation toolkit and mental health literacy in the CF community – a two-phase qualitative investigation to assess the level of need in collaboration with clinicians and PWCF.
Please note Applicants with a 2:1 degree in Psychology (or close to completion) are strongly encouraged to apply.
Please note, the successful candidate will be required to obtain AccessNI clearance prior to registration due to the nature of the project.
Applicants should hold, or expect to obtain, a First or Upper Second Class Honours Degree in a subject relevant to the proposed area of study.
We may also consider applications from those who hold equivalent qualifications, for example, a Lower Second Class Honours Degree plus a Master’s Degree with Distinction.
In exceptional circumstances, the University may consider a portfolio of evidence from applicants who have appropriate professional experience which is equivalent to the learning outcomes of an Honours degree in lieu of academic qualifications.
If the University receives a large number of applicants for the project, the following desirable criteria may be applied to shortlist applicants for interview.
The University is an equal opportunities employer and welcomes applicants from all sections of the community, particularly from those with disabilities.
Appointment will be made on merit.
This project is funded by:
Our fully funded PhD scholarships will cover tuition fees and provide a maintenance allowance of £19,237 (tbc) per annum for three years (subject to satisfactory academic performance). A Research Training Support Grant (RTSG) of £900 per annum is also available.
These scholarships, funded via the Department for the Economy (DfE) and the Vice Chancellor’s Research Scholarships (VCRS), are open to applicants worldwide, regardless of residency or domicile.
Applicants who already hold a doctoral degree or who have been registered on a programme of research leading to the award of a doctoral degree on a full-time basis for more than one year (or part-time equivalent) are NOT eligible to apply for an award.
Due consideration should be given to financing your studies.
Abbott, J., Morton, A., Hart, A., Conway, S. P., & Webb, A. K. (2007). 313 Can patient-reported health-related quality of life predict survival in cystic fibrosis?. Journal of Cystic Fibrosis, 6, 77.
Bach, M., Jordan, S., Hartung, S., Santos-Hövener, C., & Wright, M. T. (2017). Participatory epidemiology: the contribution of participatory research to epidemiology. Emerging Themes in Epidemiology, 14(1), 1-15.
Bathgate, C. J., Hjelm, M., Filigno, S. S., Smith, B. A., & Georgiopoulos, A. M. (2022). Management of Mental Health in Cystic Fibrosis. Clinics in Chest Medicine, 43(4), 791-810.
Birnie, K. A., Noel, M., Chambers, C. T., Uman, L. S., & Parker, J. A. (2018). Psychological interventions for needle‐related procedural pain and distress in children and adolescents. Cochrane Database of Systematic Reviews, (10).
Cronly, J., Duff, A., Riekert, K., Horgan, A., Lehane, E., Perry, I., ... & Savage, E. (2019). Positive mental health and wellbeing in adults with cystic fibrosis: A cross sectional study. Journal of Psychosomatic Research, 116, 125-130.
Latchford, G., & Duff, A. J. (2013). Screening for depression in a single CF centre. Journal of Cystic Fibrosis, 12(6), 794-796.
Melhuish, L. S. (2012). Eating attitudes and behaviours in males and females with cystic fibrosis: the role of body image and coping styles (Doctoral dissertation, University of Southampton).
McHugh, R., Vaughan, R. S., Duarte, C., McDevitt-Petrovic, O., & Kirby, K. (2023). Psychometric properties of the cystic fibrosis eating attitudes and behaviours scale (CFEAB) in an adult population. Journal of Psychosomatic Research, 111123.
Mc Hugh, R., Mc Feeters, D., Boyda, D., & O’Neill, S. (2016). Coping styles in adults with cystic fibrosis: implications for emotional and social quality of life. Psychology, Health & Medicine, 21(1), 102-112.
Polenakovik, H. M., & Sanville, B. (2013). The use of ivacaftor in an adult with severe lung disease due to cystic fibrosis (ΔF508/G551D). Journal of Cystic Fibrosis, 12(5), 530-531.
Smith, B. A., Modi, A. C., Quittner, A. L., & Wood, B. L. (2010). Depressive symptoms in children with cystic fibrosis and parents and its effects on adherence to airway clearance. Pediatric Pulmonology, 45(8), 756-763.
Quick, V., & Chang, G. (2021). Health care provider’s experiences, practices, and recommendations for interventions and screening of cystic fibrosis patients with disordered eating: A qualitative analysis. Chronic Illness, 17(4), 377-390.
Quittner, A. L., Goldbeck, L., Abbott, J., Duff, A., Lambrecht, P., Solé, A., ... & Barker, D. (2014). Prevalence of depression and anxiety in patients with cystic fibrosis and parent caregivers: results of The International Depression Epidemiological Study across nine countries. Thorax, 69(12), 1090-1097.
Quittner, A. L., Abbott, J., Georgiopoulos, A. M., Goldbeck, L., Smith, B., Hempstead, S. E., & Elborn, S. (2016). International committee on mental health in cystic fibrosis: cystic fibrosis foundation and European cystic fibrosis society consensus statements for screening and treating depression and anxiety. Thorax, 71(1), 26-34.
Uman, L. S., Chambers, C. T., McGrath, P. J., & Kisely, S. R. (2006). Psychological interventions for needle‐related procedural pain and distress in children and adolescents. Cochrane database of systematic reviews, (4).
Submission deadline
Monday 3 February 2025
04:00PM
Interview Date
10-12 March 2025
Preferred student start date
15 September 2025
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