Yr Athro Christine Bundy

PhD, AFBPS C Psychol (Health)

Articles

• Navarro‐Compán, V. et al. 2024. Females with axial spondyloarthritis have longer diagnostic delay and higher burden of the disease. Results from the International Map of Axial Spondyloarthritis (IMAS). International Journal of Rheumatic Diseases 27(12), article number: e15433. (10.1111/1756-185x.15433)
• Garrido-Cumbrera, M. et al. 2024. Do patients with axial spondyloarthritis with active disease suffer from greater disease burden and work impairment? Results from the International Map of Axial Spondyloarthritis (IMAS). Reumatología Clínica (English Edition) 20(10), pp. 547-554. (10.1016/j.reumae.2024.11.009)
• Whybrow, D., Jones, B., Temeng, E., Dale, C., Bundy, C. and Watts, T. 2024. The perceived helpfulness and acceptability of a bespoke psychological therapy service for registered nurses experiencing psychological distress: A qualitative study. Journal of Advanced Nursing 80(12), pp. 5029-5038. (10.1111/jan.16160)
• Thomas, B. et al. 2024. Defining and measuring Long COVID fatigue – a scoping review. BMJ Open 14, article number: e088530. (10.1136/bmjopen-2024-088530)
• Thomas, B., Pattinson, R., Bundy, C. and Davies, J. L. 2024. Somatosensory processing in long COVID fatigue and its relations with physiological and psychological factors. Experimental Physiology 109(10), pp. 1637-1649. (10.1113/ep091988)
• Dale, C., Hewitt, R. M., Purcell, C., Pandya, N. and Bundy, C. 2024. 'Feeling like a second-class citizen': exploring the impact, self-management and existing support for adults living with acne and/or post-inflammatory hyperpigmentation and scarring. British Journal of Dermatology 191(3), pp. 469-470. (10.1093/bjd/ljae190)
• Poddubnyy, D. et al. 2024. Diagnostic delay in patients from the international map of axial spondyloarthritis: geographic, socio-demographic and disease-related factors. Rheumatology (10.1093/rheumatology/keae521)
• Garrido-Cumbrera, M. et al. 2024. Regional differences in diagnosis journey and healthcare utilization: Results from the International Map of Axial Spondyloarthritis (IMAS). Rheumatology and Therapy 11(4), pp. 927-945. (10.1007/s40744-024-00672-3)
• Hewitt, R. M., Dale, C., Purcell, C., Pattinson, R. and Bundy, C. 2024. A qualitative exploration of the impact, management, and existing psychological support available for adults living with skin conditions. Acta Dermato-Venereologica 104, article number: adv40657. (10.2340/actadv.v104.40657)
• Elliott, J., Hodges, C., Boots, M., Pattinson, R., Gillen, E., Whybrow, D. and Bundy, C. 2024. Mixed shift rotations, sleep, burnout and well-being in professions similar to radiographers: A systematic review. Radiography 30(4), pp. 1194-1200. (10.1016/j.radi.2024.05.016)
• Trialonis‐Suthakharan, N. et al. 2024. Patient prioritisation of items to develop the Patient‐Reported Impact of Dermatological Diseases measure: A global Delphi study. Journal of the European Academy of Dermatology and Venereology 38(7), pp. 1391-1400. (10.1111/jdv.19903)
• Pattinson, R., Trialonis-Suthakaran, N., Pickles, T., Austin, J., FitzGerald, A., Augustin, M. and Bundy, C. 2024. Measurement properties and interpretability of the Patient-Reported Impact of Dermatological Diseases (PRIDD) measure. British Journal of Dermatology (10.1093/bjd/ljae267)
• Garrido-Cumbrera, M. et al. 2024. Factors associated with poor mental health in patients with axial spondyloarthritis: results from the International Map of Axial Spondyloarthritis (IMAS). RMD Open 10(2), article number: e004218. (10.1136/rmdopen-2024-004218)
• Garrido-Cumbrera, M. et al. 2024. International Map of Axial Spondyloarthritis (IMAS): results from the perspective of 5557 patients from 27 countries around the globe. RMD Open 10, article number: e003504. (10.1136/rmdopen-2023-003504)
• Pattinson, R., Trialonis-Suthakharan, N., Pickles, T., Austin, J., FitzGerald, A., Augustin, M. and Bundy, E. 2024. Further refinement of the Patient-Reported Impact of Dermatological Diseases (PRIDD) measure using classical test theory and item response theory. British Journal of Dermatology 190(5), pp. 718-728., article number: ljad487. (10.1093/bjd/ljad487)
• Thomas, B. et al. 2024. Definitions and measures of long COVID fatigue in adults: a scoping review protocol. JBI Evidence Synthesis 22(3), pp. 481-488. (10.11124/jbies-23-00277)
• Temeng, E., Hewitt, R., Pattinson, R., Sydor, A., Whybrow, D., Watts, T. and Bundy, C. 2024. Nurses' coping strategies caring for patients during severe viral pandemics: A mixed methods systematic review. Journal of Clinical Nursing. 33(1), pp. 242-254. (10.1111/jocn.16711)
• Trialonis-Suthakharan, N. et al. 2023. Patient prioritisation of impact items to develop the patient-reported impact of dermatological diseases (PRIDD) measure: European Delphi data. Journal of the European Academy of Dermatology and Venereology 37(7), pp. 40-50. (10.1111/jdv.19266)
• Watts, T. et al. 2023. Registered Nurses' and nursing students' perspectives on moral distress and its effects: a mixed-methods systematic review and thematic synthesis. Nursing Open 10(9), pp. 6014-6032. (10.1002/nop2.1913)
• Hailey, L. H. et al. 2023. Lifestyle modifications and nonpharmacologic interventions to improve outcomes in psoriatic arthritis: A systematic review. Clinical Therapeutics 45(9), pp. 841-851. (10.1016/j.clinthera.2023.05.009)
• Hailey, L. H. et al. 2023. Developing evidence-based patient focused learning materials to support health behaviour change for people living with psoriatic arthritis. RMD Open 9(3), article number: e003190. (10.1136/rmdopen-2023-003190)
• Hailey, L. et al. 2023. The top 10 research priorities in psoriatic arthritis: a James Lind alliance priority setting partnership. Rheumatology 62(8), pp. 2716-2723. (10.1093/rheumatology/keac676)
• Pattinson, R. et al. 2023. Evidence of the content validity, acceptability, and feasibility of a new patient-reported impact of dermatological diseases (PRIDD) measure. Frontiers in Medicine 10, article number: 1020523. (10.3389/fmed.2023.1020523)
• Hewitt, R. et al. 2022. Covid-19 Coping Survey: an in-depth qualitative analysis of free-text responses from people with and without existing health conditions in the UK. International Journal of Behavioral Medicine 29, pp. 743-751. (10.1007/s12529-022-10055-z)
• Hewitt, R. M., Purcell, C. and Bundy, C. 2022. Safeguarding online research integrity: concerns from recent experiences. British Journal of Dermatology 187(6), pp. 999-1000. (10.1111/bjd.21765)
• Pattinson, R. et al. 2022. Development of a conceptual framework for a patient-reported impact of dermatological diseases (PRIDD) measure: A qualitative concept elicitation study. Acta Dermato-Venereologica 102 (10.2340/actadv.v102.2401)
• Hewitt, R. M. et al. 2022. A mixed methods systematic review of digital interventions to support the psychological health and well-being of people living with dermatological conditions. Frontiers in Medicine (10.3389/fmed.2022.1024879)
• Hewitt, R. M., Urmston, D., Mcateer, H., Schofield, J. and Bundy, C. 2022. A UK online survey exploring patient perspectives of remote consultations for managing psoriasis and psoriatic arthritis during the SARS-CoV-2 pandemic. Psychology, Health and Medicine (10.1080/13548506.2022.2104883)
• Pattinson, R., Trialonis-Suthakharan, N., Tahmasebi Gandomkari, N., Valencia López, M., Austin, J., Augustin, M. and Bundy, C. 2022. P8 patient prioritisation of items for the new Patient-Reported Impact of Dermatological Diseases (PRIDD) measure: A delphi study. Value in Health 25(7), pp. S288. (10.1016/j.jval.2022.04.1726)
• Hewitt, R. M. et al. 2022. How do dermatologists’ personal models inform a patient–centred approach to management: a qualitative study using the example of prescribing a new treatment (Apremilast). British Journal of Dermatology 187(1), pp. 82-88. (10.1111/bjd.21029)
• Garrido-Cumbrera, M. et al. 2022. Identifying parameters associated with delayed diagnosis in axial spondyloarthritis: data from the European map of axial spondyloarthritis. Rheumatology 61(2), pp. 705-712., article number: keab369. (10.1093/rheumatology/keab369)
• Hewitt, R. M., Pattinson, R., Daniel, R., Carrier, J., Sanders, O. and Bundy, C. 2022. Online survey comparing coping responses to SARS-CoV-2 by people with and without existing health conditions in the UK. BMJ Open 12(2), article number: e051575. (10.1136/bmjopen-2021-051575)
• Pattinson, R., Trialonis-Suthakharan, N., Austin, J., Augustin, M. and Bundy, C. 2022. POSB369 development of the patient-reported impact of dermatological diseases (PRIDD) measure. Value in Health 25(1), article number: S232. (10.1016/j.jval.2021.11.1136)
• Pattinson, R., Poole, H. M., Shorthouse, O., Sadiq, S. A. and Bundy, C. 2022. Exploring beliefs and distress in patients with facial palsies. Psychology, Health and Medicine 27(4), pp. 788-802. (10.1080/13548506.2021.1876891)
• Garrido-Cumbrera, M. et al. 2021. Patient‐reported impact of axial spondyloarthritis on working life: results from the EMAS survey. Arthritis Care and Research 73(12), pp. 1826-1833. (10.1002/acr.24426)
• Hewitt, R. M. and Bundy, C. 2021. New technology use needs patient input. British Journal of Dermatology 185(5), pp. 880-881. (10.1111/bjd.20634)
• Pattinson, R. L. et al. 2021. Patient-reported outcome measures in dermatology: a systematic review. Acta Dermato-Venereologica 101(9), article number: adv00559. (10.2340/00015555-3884)
• Garrido-Cumbrera, M. et al. 2021. Impact of axial spondyloarthritis on mental health in Europe: results from the EMAS study. RMD Open 7(3), article number: e001769. (10.1136/rmdopen-2021-001769)
• Garrido-Cumbrera, M. et al. 2021. Gender differences in patient journey to diagnosis and disease outcomes: results from the European Map of Axial Spondyloarthritis (EMAS). Clinical Rheumatology 40(7), pp. 2753-2761. (10.1007/s10067-020-05558-7)
• Gratacós, J. et al. 2021. A 12-point recommendation framework to support advancement of the multidisciplinary care of psoriatic arthritis: a call to action. Joint Bone Spine 88(3), article number: 105175. (10.1016/j.jbspin.2021.105175)
• Hewitt, R. M. et al. 2021. Implementation of the PsoWell™ model for the management of people with complex psoriasis. Acta Dermato-Venereologica 101(4), article number: adv00445. (10.2340/00015555-3802)
• Barton, A. et al. 2021. Translating research into clinical practice: quality improvement to halve non-adherence to methotrexate. Rheumatology 60(1), pp. 125–131. (10.1093/rheumatology/keaa214)
• Augustin, M. et al. 2021. Characteristics and outcomes of patients treated with apremilast in the real world: results from the APPRECIATE study. Journal of the European Academy of Dermatology and Venereology 35(1), pp. 123-134. (10.1111/jdv.16431)
• Hewitt, R., Pattinson, R., Sanders, O. and Bundy, E. 2020. The importance of source credibility for recruiting underrepresented groups in health research: Insights from the Covid-19 coping survey. Health Psychology Update 29, pp. 48-49.
• Kleyn, C. et al. 2020. Psoriasis and mental health workshop report: exploring the links between psychosocial factors, psoriasis, neuroinflammation and cardiovascular disease risk. Acta Dermato-Venereologica 100, pp. 1-8., article number: 20. (10.2340/00015555-3375)
• Sadiq, S. A., Pattinson, R., Poole, H. M. and Bundy, C. 2020. Psychological distress and coping following eye removal surgery. Orbit 39(3), pp. 175-182. (10.1080/01676830.2019.1658789)
• Henry, A. L., Bundy, C., Kyle, S. D., Griffiths, C. E. M. and Chisholm, A. 2019. Understanding the experience of sleep disturbance in psoriasis:a qualitative exploration using the Common-Sense Model of Self-Regulation. British Journal of Dermatology 180(6), pp. 1397-1404. (10.1111/bjd.17685)
• Keyworth, C., Nelson, P. A., Bundy, C., Pye, S. R., Griffiths, C. E. M. and Cordingley, L. 2018. Does message framing affect changes in behavioural intentions in people with psoriasis? A randomized exploratory study examining health risk communication. Psychology, Health and Medicine 23(7), pp. 763-778. (10.1080/13548506.2018.1427876)
• Boots, M. C., Button, K. and Bundy, C. 2017. Exploring practice & clinical evidence with pre-manipulative testing for cervical arterial dysfunction amongst musculoskeletal physiotherapists within a Welsh Health Board. Physiotherapy 103(1), article number: e110. (10.1016/j.physio.2017.11.088)
• Howells, L., Chisholm, A., Cotterill, S., Chinoy, H., Warren, R. B. and Bundy, C. 2017. Impact of disease severity, illness beliefs, and coping strategies on outcomes in psoriatic arthritis. Arthritis Care & Research 70(2), pp. 295-302. (10.1002/acr.23330)
• Henry, A. L., Kyle, S. D., Chisholm, A., Griffiths, C. E. M. and Bundy, C. 2017. A cross-sectional survey of the nature and correlates of sleep disturbance in people with psoriasis. British Journal of Dermatology 177(4), pp. 1052-1059. (10.1111/bjd.15469)
• Nelson, P. A. et al. 2017. 'New to me': changing patient understanding of psoriasis and identifying mechanisms of change. The Pso Well (R) patient materials mixed-methods feasibility study. British Journal of Dermatology 177(3), pp. 758-770. (10.1111/bjd.15574)
• Chisholm, A. et al. 2017. Motivational interviewing-based training enhances clinicians' skills and knowledge in psoriasis: findings from the Pso Well® study. British Journal of Dermatology 176(3), pp. 677-686. (10.1111/bjd.14837)
• Thorneloe, R. J., Bundy, C., Griffiths, C. E. M., Ashcroft, D. M. and Cordingley, L. 2017. Nonadherence to psoriasis medication as an outcome of limited coping resources and conflicting goals: findings from a qualitative interview study with people with psoriasis. British Journal of Dermatology 176(3), pp. 667-676. (10.1111/bjd.15086)
• Theodorakopoulou, E. et al. 2016. Early- and late-onset psoriasis: a cross-sectional clinical and immunocytochemical investigation. British Journal of Dermatology 175(5), pp. 1038-1044. (10.1111/bjd.14886)
• Pattinson, R. et al. 2016. Stress perception impacts on clinical signs of skin ageing and modifies the epigenome. Journal of Investigative Dermatology 136(9), pp. S171., article number: 62. (10.1016/j.jid.2016.06.079)
• Ferguson, F., Henry, A. L., Hunter, H., Bundy, C., Griffiths, C. E. M. and Kleyn, E. 2016. Diurnal and seasonal variation in psoriasis symptoms [Abstract]. British Journal of Dermatology 175(S1), pp. 50-50., article number: P56. (10.1111/bjd.14524)
• Chisholm, A. et al. 2016. Evaluation of the IMPACT study practitioner training intervention: using motivational interviewing to optimize self-management in psoriasis [Abstract]. British Journal of Dermatology 175(S1), pp. 205-205. (10.1111/bjd.14577)
• Bundy, C., Pearce, C., Sergent, J. and Griffiths, C. E. M. 2016. Obesity, low mood, negative beliefs about illness and severity of psoriasis are linked to dysfunctional eating patterns [Abstract]. British Journal of Dermatology 175(S1), pp. 205-206. (10.1111/bjd.14577)
• Henry, A. L., Kyle, S. D., Chisholm, A., Griffiths, C. E. M. and Bundy, E. 2016. A survey of sleep disturbance in psoriasis [Abstract]. British Journal of Dermatology 175(S1), pp. 206-206. (10.1111/bjd.14577)
• Nelson, P. A. et al. 2016. Development and evaluation of the IMPACT programme patient resources to increase understanding of psoriasis and its management: a mixed-methods feasibility study [Abstract]. British Journal of Dermatology 175(S1), pp. 210-210. (10.1111/bjd.14577)
• Howells, L., Chisholm, A., Cotterill, S., Chinoy, H., Warren, R. and Bundy, C. 2016. The role of beliefs, mood, coping strategies, disease severity and quality of life in patients living with psoriatic arthritis [Abstract]. British Journal of Dermatology 175(S1), pp. 53., article number: P62. (10.1111/bjd.14524)
• Hudson, J. L., Bundy, C., Coventry, P., Dickens, C., Wood, A. and Reeves, D. 2016. What are the combined effects of negative emotions and illness cognitions on self-care in people with type 2 diabetes? A longitudinal structural equation model. Psychology and Health 31(7), pp. 873-890. (10.1080/08870446.2016.1156113)
• Bundy, C. 2016. The role of clinicians, patients and social factors in poor adherence: creating new understanding and consultation skills to increase adherence and self-management psoriasis patients. Journal of the European Academy of Dermatology and Venereology 30(S6), pp. 24., article number: P034. (10.1111/jdv.13709)
• Henry, A. L., Kyle, S. D., Bhandari, S., Chisholm, A., Griffiths, C. E. M. and Bundy, C. 2016. Measurement, classification and evaluation of sleep disturbance in psoriasis: a systematic review. PLoS ONE 11(6), article number: e0157843. (10.1371/journal.pone.0157843)
• Bundy, C. 2016. Is education enough to improve quality of life in people with chronic inflammatory skin conditions?. British Journal of Dermatology 174(6), pp. 1179-1179. (10.1111/bjd.14611)
• Chisholm, A., Pearce, C. J., Chinoy, H., Warren, R. B. and Bundy, C. 2016. Distress, misperceptions, poor coping and suicidal ideation in psoriatic arthritis: a qualitative study. Rheumatology 55(6), pp. 1047-1052. (10.1093/rheumatology/kew009)
• Thaci, D. et al. 2016. Improvements in health-related quality of life and symptoms of depression with tofacitinib: results from two randomized phase 3 studies in patients with moderate to severe psoriasis. Journal of the American Academy of Dermatology 74(5:S1), pp. AB255-AB255. (10.1016/j.jaad.2016.02.992)
• Henry, A. L., Bundy, C. and Kyle, S. D. 2016. A call for improved sleep research in psoriasis populations. International Journal of Dermatology 55(5), pp. e312. (10.1111/ijd.13192)
• Betteridge, N., Boehncke, W., Bundy, C., Gossec, L., Gratacos, J. and Augustin, M. 2016. Promoting patient-centred care in psoriatic arthritis: a multidisciplinary European perspective on improving the patient experience. Journal of the European Academy of Dermatology and Venereology 30(4), pp. 576-585. (10.1111/jdv.13306)
• Schwartz, J., Evers, A. W. M., Bundy, C. and Kimball, A. B. 2016. Getting under the skin: report from the International Psoriasis Council workshop on the role of stress in psoriasis. Frontiers in Psychology 7, article number: 87. (10.3389/fpsyg.2016.00087)
• Chisholm, A., Nelson, P. A., Pearce, C. J., Keyworth, C., Griffiths, C. E. M., Cordingley, L. and Bundy, C. 2016. The role of personal models in clinical management: exploring health care providers' beliefs about psoriasis. British Journal of Health Psychology 21(1), pp. 114-134. (10.1111/bjhp.12148)
• Kitchen, H., Cordingley, L., Young, H., Griffiths, C. and Bundy, C. 2015. Content development and refinement for a new Patient reported outcome measure for Psoriasis Treatment (PROMPT). Value in Health 18(3), pp. A184-A185. (10.1016/j.jval.2015.03.1067)
• Bundy, C. 2015. Practitioners need input from behavioural medicine specialists. BMJ 2015(315), article number: h5291. (10.1136/bmj.h5291)
• Kitchen, H., Cordingley, L., Gibbons, C., Young, H., Griffiths, C. and Bundy, C. 2015. Rasch analysis of a new Patient Reported Outcome Measure for Psoriasis Treatment (PROMPT). Value in Health 18(3), pp. A184-A184. (10.1016/j.jval.2015.03.1066)
• Nelson, P. et al. 2015. The IMPACT Programme in Psoriasis: Phase I - where we are now and future directions. Dermatological Nursing 14(4), pp. 37-44.

Conferences

• Watts, T. et al. 2023. ASSISTANCE (Addressing moral distress among nurses after the COVID-19 emergency): co-creation of evidence-based guidance to ameliorate moral distress.. Presented at: Chief Nursing Office Wales Conference, Cardiff, 13 October 2023.
• Watts, T. et al. 2023. Addressing moral distress among nurses after the Covid-19 emergency: The ASSISTANCE study. Presented at: Chief Nursing Officer Conference, Cardiff, 13 October 2023.
• Watts, T. et al. 2023. Co-creation of evidence-based moral distress guidance for nurses: The ASSISTANCE (Addressing moral distress among nurses after the COVID-19 emergency) Study -Phase 3. Presented at: Chief Nurse Conference, Cardiff, UK, 13 October 2023.
• Watts, T. et al. 2023. The ASSISTANCE STUDY: Moral distress and psychological wellbeing of nurses during the COVID-19 pandemic. Presented at: Royal College of Nursing International Nursing Research Conference, Manchester University, 6-8 September 2023.
• Watts, T. et al. 2022. Perceived helpfulness of a tiered mental health support intervention for moral distress: a qualitative, exploratory study. Presented at: European Nursing Congress 22: Future Proof Nursing: Nurses as key drivers of change, Netherlands, 4-7 October 2022.
• Watts, T. et al. 2022. Contributing factors and impacts of moral distress among nurses: a systematic review. Presented at: European Nursing Congress 22: Future Proof Nursing: Nurses as key drivers of change, Netherlands, 4-7 October 2022.
• Watts, T. et al. 2022. Symposium of four papers: Identifying and mitigating moral distress in the nursing workforce: insights from the UK and the United States. Presented at: RCN International Nursing Research Conference, Cardiff, UK, 5-6 Sept 2022.
• Temeng, E., Hewitt, R., Pattinson, R., Sydor, A., Whybrow, D., Watts, T. and Bundy, E. 2022. Nurses' experiences of caring for severely ill patients during infection outbreaks (pandemic / epidemic): a mixed methods systematic review. Presented at: RCN International Nursing Research Conference 2022, Cardiff, 5-6 September 2022.
• Boots, M., Button, K. and Bundy, C. 2021. Exploring public perception of brief interventions for physical activity, for the management of musculoskeletal pain, in Wales. Physiotherapy. Presented at: Virtual Physiotherapy UK conference, Online. Elsevier, (10.1016/j.physio.2021.10.058)
• Watts, T. et al. 2021. Supportive interventions to mitigate moral distress among nurses: a mixed methods systematic review and narrative synthesis. Presented at: Public Health Wales Research and Evaluation Conference 2021: Research in action: COVID-19 and beyond, Online, 23 September 2021.
• Kleyn, E. et al. 2017. Real-world experience with apremilast in patients with psoriasis: interim analysis of 104 patients from the APPRECIATE study. Presented at: Psoriasis Gene to Clinic, 8th International Congress, The Queen Elizabeth II Conference Centre, London, U.K, 30th Nov – 2nd Dec 2017British Journal of Dermatology, Vol. 177. Vol. 5. Wiley-Blackwell pp. E244., (10.1111/bjd.16059)

Monographs

• Watts, T. et al. 2022. Addressing moral distress during COVID-19 recovery: a mixed methods systematic review and narrative synthesis of moral distress in nurses and supportive moral distress interventions. Public Health Wales: Cardiff University.

• Keyworth, C., Nelson, P. A., Bundy, C., Pye, S. R., Griffiths, C. E. M. and Cordingley, L. 2018. Does message framing affect changes in behavioural intentions in people with psoriasis? A randomized exploratory study examining health risk communication. Psychology, Health and Medicine 23(7), pp. 763-778. (10.1080/13548506.2018.1427876)
• Howells, L., Chisholm, A., Cotterill, S., Chinoy, H., Warren, R. B. and Bundy, C. 2017. Impact of disease severity, illness beliefs, and coping strategies on outcomes in psoriatic arthritis. Arthritis Care & Research 70(2), pp. 295-302. (10.1002/acr.23330)
• Kleyn, E. et al. 2017. Real-world experience with apremilast in patients with psoriasis: interim analysis of 104 patients from the APPRECIATE study. Presented at: Psoriasis Gene to Clinic, 8th International Congress, The Queen Elizabeth II Conference Centre, London, U.K, 30th Nov – 2nd Dec 2017British Journal of Dermatology, Vol. 177. Vol. 5. Wiley-Blackwell pp. E244., (10.1111/bjd.16059)
• Henry, A. L., Kyle, S. D., Chisholm, A., Griffiths, C. E. M. and Bundy, C. 2017. A cross-sectional survey of the nature and correlates of sleep disturbance in people with psoriasis. British Journal of Dermatology 177(4), pp. 1052-1059. (10.1111/bjd.15469)
• Nelson, P. A. et al. 2017. 'New to me': changing patient understanding of psoriasis and identifying mechanisms of change. The Pso Well (R) patient materials mixed-methods feasibility study. British Journal of Dermatology 177(3), pp. 758-770. (10.1111/bjd.15574)
• Thorneloe, R. J., Bundy, C., Griffiths, C. E. M., Ashcroft, D. M. and Cordingley, L. 2017. Nonadherence to psoriasis medication as an outcome of limited coping resources and conflicting goals: findings from a qualitative interview study with people with psoriasis. British Journal of Dermatology 176(3), pp. 667-676. (10.1111/bjd.15086)
• Pattinson, R. et al. 2016. Stress perception impacts on clinical signs of skin ageing and modifies the epigenome. Journal of Investigative Dermatology 136(9), pp. S171., article number: 62. (10.1016/j.jid.2016.06.079)
• Ferguson, F., Henry, A. L., Hunter, H., Bundy, C., Griffiths, C. E. M. and Kleyn, E. 2016. Diurnal and seasonal variation in psoriasis symptoms [Abstract]. British Journal of Dermatology 175(S1), pp. 50-50., article number: P56. (10.1111/bjd.14524)
• Chisholm, A. et al. 2016. Evaluation of the IMPACT study practitioner training intervention: using motivational interviewing to optimize self-management in psoriasis [Abstract]. British Journal of Dermatology 175(S1), pp. 205-205. (10.1111/bjd.14577)
• Bundy, C., Pearce, C., Sergent, J. and Griffiths, C. E. M. 2016. Obesity, low mood, negative beliefs about illness and severity of psoriasis are linked to dysfunctional eating patterns [Abstract]. British Journal of Dermatology 175(S1), pp. 205-206. (10.1111/bjd.14577)
• Henry, A. L., Kyle, S. D., Chisholm, A., Griffiths, C. E. M. and Bundy, E. 2016. A survey of sleep disturbance in psoriasis [Abstract]. British Journal of Dermatology 175(S1), pp. 206-206. (10.1111/bjd.14577)
• Nelson, P. A. et al. 2016. Development and evaluation of the IMPACT programme patient resources to increase understanding of psoriasis and its management: a mixed-methods feasibility study [Abstract]. British Journal of Dermatology 175(S1), pp. 210-210. (10.1111/bjd.14577)
• Howells, L., Chisholm, A., Cotterill, S., Chinoy, H., Warren, R. and Bundy, C. 2016. The role of beliefs, mood, coping strategies, disease severity and quality of life in patients living with psoriatic arthritis [Abstract]. British Journal of Dermatology 175(S1), pp. 53., article number: P62. (10.1111/bjd.14524)
• Hudson, J. L., Bundy, C., Coventry, P., Dickens, C., Wood, A. and Reeves, D. 2016. What are the combined effects of negative emotions and illness cognitions on self-care in people with type 2 diabetes? A longitudinal structural equation model. Psychology and Health 31(7), pp. 873-890. (10.1080/08870446.2016.1156113)
• Bundy, C. 2016. The role of clinicians, patients and social factors in poor adherence: creating new understanding and consultation skills to increase adherence and self-management psoriasis patients. Journal of the European Academy of Dermatology and Venereology 30(S6), pp. 24., article number: P034. (10.1111/jdv.13709)
• Henry, A. L., Kyle, S. D., Bhandari, S., Chisholm, A., Griffiths, C. E. M. and Bundy, C. 2016. Measurement, classification and evaluation of sleep disturbance in psoriasis: a systematic review. PLoS ONE 11(6), article number: e0157843. (10.1371/journal.pone.0157843)
• Bundy, C. 2016. Is education enough to improve quality of life in people with chronic inflammatory skin conditions?. British Journal of Dermatology 174(6), pp. 1179-1179. (10.1111/bjd.14611)
• Chisholm, A., Pearce, C. J., Chinoy, H., Warren, R. B. and Bundy, C. 2016. Distress, misperceptions, poor coping and suicidal ideation in psoriatic arthritis: a qualitative study. Rheumatology 55(6), pp. 1047-1052. (10.1093/rheumatology/kew009)
• Thaci, D. et al. 2016. Improvements in health-related quality of life and symptoms of depression with tofacitinib: results from two randomized phase 3 studies in patients with moderate to severe psoriasis. Journal of the American Academy of Dermatology 74(5:S1), pp. AB255-AB255. (10.1016/j.jaad.2016.02.992)
• Henry, A. L., Bundy, C. and Kyle, S. D. 2016. A call for improved sleep research in psoriasis populations. International Journal of Dermatology 55(5), pp. e312. (10.1111/ijd.13192)
• Betteridge, N., Boehncke, W., Bundy, C., Gossec, L., Gratacos, J. and Augustin, M. 2016. Promoting patient-centred care in psoriatic arthritis: a multidisciplinary European perspective on improving the patient experience. Journal of the European Academy of Dermatology and Venereology 30(4), pp. 576-585. (10.1111/jdv.13306)
• Schwartz, J., Evers, A. W. M., Bundy, C. and Kimball, A. B. 2016. Getting under the skin: report from the International Psoriasis Council workshop on the role of stress in psoriasis. Frontiers in Psychology 7, article number: 87. (10.3389/fpsyg.2016.00087)
• Chisholm, A., Nelson, P. A., Pearce, C. J., Keyworth, C., Griffiths, C. E. M., Cordingley, L. and Bundy, C. 2016. The role of personal models in clinical management: exploring health care providers' beliefs about psoriasis. British Journal of Health Psychology 21(1), pp. 114-134. (10.1111/bjhp.12148)
• Kitchen, H., Cordingley, L., Young, H., Griffiths, C. and Bundy, C. 2015. Content development and refinement for a new Patient reported outcome measure for Psoriasis Treatment (PROMPT). Value in Health 18(3), pp. A184-A185. (10.1016/j.jval.2015.03.1067)
• Bundy, C. 2015. Practitioners need input from behavioural medicine specialists. BMJ 2015(315), article number: h5291. (10.1136/bmj.h5291)
• Kitchen, H., Cordingley, L., Gibbons, C., Young, H., Griffiths, C. and Bundy, C. 2015. Rasch analysis of a new Patient Reported Outcome Measure for Psoriasis Treatment (PROMPT). Value in Health 18(3), pp. A184-A184. (10.1016/j.jval.2015.03.1066)
• Nelson, P. et al. 2015. The IMPACT Programme in Psoriasis: Phase I - where we are now and future directions. Dermatological Nursing 14(4), pp. 37-44.