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Number of items: 35.


Dures, E., Hewlett, S., Almeida, C. and Pollock, J. (2017) Patients’ perspectives on the psychological impact of inflammatory arthritis and meeting the associated support needs: Open-ended responses in a multi-centre survey. Musculoskeletal Care, 15 (3). pp. 175-185. ISSN 1478-2189 Available from:

Tillett, W., Dures, E., Hewlett, S., Helliwell, P., FitzGerald, O., Brooke, M., James, J., Lord, J., Bowen, C., de Wit, M., Orbai, A. and McHugh, N. (2017) A multicentre nominal group study to rank outcomes important to patients and their representation in existing composite outcome measures for psoriatic arthritis. Journal of Rheumatology, 44 (10). ISSN 0315-162X Available from:

Dures, E., Hewlett, S., Lord, J., Bowen, C., McHugh, N. and Tillett, W. (2017) Important treatment outcomes for patients with psoriatic arthritis: A multi-site qualitative study. The Patient - Patient-Centered Outcomes Research, 10 (4). pp. 455-462. ISSN 1178-1653 Available from:

Orbai, A.-M., de Witt, M., Mease, P., Shea, J., Gossec, L., Leung, Y. Y., Tillett, W., Elmamoum, M., Duffin, K., Campbell, W., Christensent, R., Coates, L., Dures, E., Eder, L., Fitzgerald, O., Gladman, D., Goel, N., Grieg, S., Hewlett, S., Hoejgaard, P., Kalyoncu, U., Lindsay, C., McHugh, N., Shea, B., Steinkoenig, I., Strand, V. and Ogdie, A. (2017) International patient and physician consensus on a psoriatic arthritis core outcome set for clinical trials. Annals of the Rheumatic Diseases, 76 (4). pp. 673-680. ISSN 0003-4967 Available from:

Hewlett, S., Kirwan, J., Bode, C., Cramp, F., Dures, E., Englbrecht, M., Fransen, J., Greenwood, R., Hagel, S., Van de Laar, M., Molto, A., Nicklin, J., Petersson, I., Redondo, M., Schett, G. and Gossec, L. (2017) Validity of the Bristol RA fatigue multi-dimensional questionnaire, numerical rating scales V2 and RA impact of disease scale in 6 countries. Rheumatology. ISSN 1462-0324 [In Press] Available from:

Wilson, O., Kirkwan, J., Dures, E., Quest, E. and Hewlett, S. (2017) The experience of foot problems and decisions to access foot care in patients with rheumatoid arthritis: A qualitative study. Journal of Foot and Ankle Research, 10 (4). ISSN 1757-1146 Available from:

Halls, S., Dures, E., Kirwan, J., Pollock, J., Baker, G., Edmunds, A. and Hewlett, S. (2017) “We only talk about the morning because that’s what you ask us”: Qualitative development and cognitive testing of candidate items for inclusion in a new rheumatoid arthritis stiffness patient-reported outcome measure. Rheumatology. ISSN 1462-0324 [In Press] Available from:


Dures, E., Almeida, C., Caesley, J., Peterson, A., Ambler, N., Morris, M., Pollock, J. and Hewlett, S. (2016) Patient preferences for psychological support in inflammatory arthritis: A multicentre survey. Annals of the Rheumatic Diseases, 75 (1). pp. 142-147. ISSN 0003-4967 Available from:

Hewlett, S., Nicklin, J., Bode, C., Carmona, L., Dures, E., Engelbrecht, M., Hagel, S., Kirwan, J., MOLTO, A., Redondo, M. and Gossec, L. (2016) Translating patient reported outcome measures: Methodological issues explored using cognitive interviewing with three rheumatoid arthritis measures in 6 European languages. Rheumatology, 55 (6). pp. 1009-1016. ISSN 1462-0324 Available from:

Dures, E., Hewlett, S., Ambler, N., Jenkins, R., Clarke, J. and Gooberman-Hill, R. (2016) A qualitative study of patients’ perspectives on collaboration to support self-management in routine rheumatology consultations. BMC Musculoskeletal Disorder, 17. pp. 129-137. ISSN 1471-2474 Available from:


Hewlett, S., Ambler, N., Almeida, C., Blair, P. S., Choy, E., Dures, E., Hammond, A., Hollingworth, W., Kirwan, J., Plummer, Z., Rooke, C., Thorn, J., Tomkinson, K. and Pollock, J. (2015) Protocol for a randomised controlled trial for Reducing Arthritis Fatigue by clinical Teams using cognitive behavioural approaches (RAFT). BMJ Open, 5 (8). ISSN 2044-6055 Available from:

Halls, S., Dures, E., Kirwan, J. R., Pollock, J., Baker, G., Edmunds, A. and Hewlett, S. (2015) Stiffness is more than just duration and severity: A qualitative exploration in people with rheumatoid arthritis. Rheumatology, 54 (4). pp. 615-622. ISSN 1462-0324 Available from:


Dures, E., Almeida, C., Caesley, J., Peterson, A., Ambler, N., Morris, M., Pollock, J. and Hewlett, S. (2014) A survey of psychological support provision for people with inflammatory arthritis in secondary care in England. Musculoskeletal Care, 12 (3). pp. 173-181. ISSN 1478-2189 Available from:

Dures, E. (2014) Behaviour change techniques to facilitate patients' self-management of their rheumatic disease. In: International Congress of Behavioural Medicine, Groningen, The Netherlands, 20-23 August, 2014. Available from:

Dures, E., Hewlett, S., Ambler, N., Jenkins, R., Clarke, J. and Gooberman-Hill, R. (2014) Rheumatology clinicians’ experiences of brief training and implementation of skills to support patient self-management. BMC Musculoskeletal Disorders, 15 (3). p. 108. ISSN 1471-2474 Available from:


Dures, E. (2013) Using psychological approaches in the clinical setting: What can we do and how? In: Eurpoean League Against Rheumatism (EULAR) 2013, Madrid, Spain, 12-15 June, 2013. Available from:

Dures, E. (2013) Introducing cognitive-behavioural approaches to rheumatic disease: Top tips and tools for clinic. In: Dures, E., ed. Rheumatology 2013, Birmingham, United Kingdom, 23-25 April, 2013. Available from:

Dures, E., Rumsey, N., Morris, M. and Gleeson, K. (2013) A cross sectional, observational survey to assess levels and predictors of psychological wellbeing in adults with epidermolysis bullosa (EB). Health Psychology Research, 1 (e4). pp. 16-20. ISSN 2281-2075 Available from:

Dures, E., Hewlett, S., Cramp, F. A., Greenwood, R., Nicklin, J. K., Urban, M. and Kirwan, J. R. (2013) Reliability and sensitivity to change of the Bristol Rheumatoid Arthritis Fatigue scales. Rheumatology, 52 (10). pp. 1832-1839. ISSN 1462-0324 Available from:


Dures, E. (2012) New and better habits! Facilitating patient self-management with proven behavior change strategies. In: 2012 ACR/ARHP Annual Meeting, Washington, DC, USA, 10-14 November , 2012. Available from:

Bessell, A., Dures, E., Semple, C. and Jackson, S. (2012) The need to address appearance-related distress across clinical conditions: How can healthcare teams support patients? British Journal of Nursing , 21 (19). pp. 1138-1143. ISSN 0966-0461 Available from:

Dures, E., Kitchen, K., Almeida, C., Ambler, N., Cliss, A., Hammond, A., Knops, B., Morris, M., Swinkels, A. and Hewlett, S. (2012) “They didn’t tell us, they made us work it out ourselves“: Patient perspectives of a cognitive-behavioural programme for rheumatoid arthritis fatigue. Arthritis Care and Research, 64 (4). pp. 494-501. ISSN 2151-4658 Available from:

Williams, L., Dures, E., Waylen, A., Ireland, T., Rumsey, N. and Sandy , J. (2012) Approaching parents to take part in a cleft gene bank: A qualitative pilot study. The Cleft Palate-Craniofacial Journal, 49 (4). pp. 425-436. ISSN 1545-1569 Available from:

Dures, E. and Hewlett, S. (2012) Cognitive–behavioural approaches to self-management in rheumatic disease. Nature Reviews Rheumatology, 8. pp. 553-559. ISSN 1759-4790 Available from:

Hewlett, S., Dures, E. and Almeida, C. (2012) Measures of fatigue. Arthritis Care and Research, 63 (S11). S263-S286. ISSN 2151-4658 Available from:


Hewlett, S., Chalder, T., Choy, E., Cramp, F. A., Davis, B., Dures, E., Nicholls, C. and Kirwan, J. R. (2011) Fatigue in rheumatoid arthritis: Time for a conceptual model (Editorial). Rheumatology, 50 (6). pp. 1004-1006. ISSN 1462-0324 Available from:

Dures, E., Morris, M., Gleeson, K. and Rumsey, N. (2011) The psychosocial impact of epidermolysis bullosa. Qualitative Health Research, 21 (6). pp. 771-782. ISSN 1049-7323 Available from:

Dures, E., Rumsey, N., Morris, M. and Gleeson, K. (2011) Mixed methods in health psychology: theoretical and practical considerations of the third paradigm. Journal of Health Psychology, 16 (2). pp. 322-341. ISSN 1359-1053 Available from:

Kirwan, J. R., Fries, J., Hewlett, S., Osborne, R., Newman, S., Ciciriello, S., van de Laar, M., Dures, E., Minnock, P., Heiberg, T., Sanderson, T., Flurey, C. A., Leong, A., Montie, P. and Richards, P. (2011) Patient perspective workshop: Moving towards OMERACT guidelines for choosing or developing instruments to measure patient reported outcomes. Journal of Rheumatology, 38 (8). pp. 1711-1715. ISSN 0315-162X Available from:

Sanderson, T., Hewlett, S., Flurey, C. A. and Dures, E. (2011) The impact triad (severity, importance and self-management) as a method of enhancing the measurement of the personal life impact of rheumatic diseases. Journal of Rheumatology, 38 (2). pp. 191-194. ISSN 0315-162X Available from:


Dures, E. (2010) Evaluating instruments developed from a patient perspective. In: OMERACT 10, Borneo, Malaysia, May 4-8, 2010. Available from:

Dures, E., Morris, M., Gleeson, K. and Rumsey, N. (2010) “You’re whatever the patient needs at the time” The impact on health and social care professionals of supporting people with Epidermolysis Bullosa. Chronic Illness, 6 (3). pp. 215-227. ISSN 1742-3953 Available from:


Dures, E. (2008) The psychosocial impact of epidermolysis bullosa: The professionals' perspective. In: DebRA International Congress, Mechelen, Belgium, October 2008. Available from:


Dures, E., Fox, F. and Bessell, A. (2007) Theoretical and practical approaches to working with people with visible differences. In: Faculty for Clinical Health Psychology Annual Conference, Sheffield, 29-30 November 2007. Available from:


Dures, E. and Rumsey, N. (2006) Fluctuations of body image states in daily life: an exploration of women’s experiences. UWE Psychology Postgraduate Papers, 3. pp. 18-23. ISSN 1747-5937 Available from:

This list was generated on Mon Oct 23 02:24:04 2017 BST.