My research interests include experiences and patient important outcomes after hip fracture, information and support needs of parents who have had a premature infant, impact of patient and public involvement in research, psychological consequences of breast cancer screening, and informed consent/shared decision-making in cancer screening programmes (breast cancer screening, cervical cancer screening and prostate cancer management programme). I have conducted systematic reviews in the following areas: psychological consequences of breast cancer screening, prevention and treatment of osteoporosis (for the NICE guideline), interventions to support parents of premature infants (incorporated into Government task force on neonatal care and into UNICEF action plan), impact of patient and public involvement in health and social care research, health beliefs and health behaviours following cholesterol screening (HTA). I have also been involved in a systematic review of informed decision making for PSA testing for prostate cancer, and more recently involved in the evaluation of patient reported outcome measures used following hip fracture.My research has used quantitative and qualitative systematic reviews, cohort studies, and qualitative methodologies. I have also developed and evaluated leaflets and training materials for the NHS screening programme.CURRENT RESEARCH PROJECTS•PROHIP: Exploring the use of patient-reported outcome measures in the field of hip fractures School of Health and Social Studies, Funded by: Royal College of Nursing, Project Start Date: 01/09/2010 Project End Date: 30/11/2012. Collaboration with Trauma Unit, Oxford University Hospitals NHS Trust.•HIPEX: Meta synthesis and interpretative phenomenology analysis of patients experience following hip fracture. PhD, ESRC 1 + 3 scholarship
I have been working with as a Research Fellow for the Royal College of Nursing (RCN) Research Institute since 2007. My current studies are PRO- Hip and Hipex, assessing the quality and acceptability of patient reported outcome measures following hip fracture and exploring the experiences of patients after hip frature. Previously I have conducted the PIRICOM study- a structured review of evidence on the conceptualisation, measurement, impact and outcomes of patient and public involvement in health and social care research; and the POPPY study - parents of premature parents – your needs, assessing the support needs, information needs and communication needs of parents that have had a premature baby. I worked as a Research Fellow for the NICE National Collaborating Centre on the Prevention and Treatment of Osteoporosis Guideline from 2005 to 2007. From 1994 to 2004 I worked as a Research Fellow at the Department of Primary Health Care, University of Oxford. The research here included a study of the psychological consequences of routine mammography, the development of breast awareness training resources for Practice Nurses, men's experiences and GP's views of asymptomatic PSA testing for prostate cancer, issues of shared decision-making around asymptomatic PSA testing, and the development of the patient information sheet for the Prostate Cancer Risk Management Programme and Cervical Screening Programme. I have also co-authored a HTA report on the impact of screening on future health promoting behaviours and health beliefs.I gained an MSc in Evidence based Health Care from Oxford University in 1999, and an MA in Applied Social Research (distinction) in 2010. I am currently doing a PhD through an ESRC scholarship.
- Staniszewska, Sophie, Brett, Jo, Simera, I., Seers, Kate, Mockford, Carole, Goodlad, S., Altman, D. G., Moher, David, Barber, R., Denegri, S., Entwistle, A., Littlejohns, P., Morris, C., Suleman, Rashida, Thomas, V., Tysall, C., 2017. GRIPP2 reporting checklists : tools to improve reporting of patient and public involvement in research. BMJ, 358
- Brett, Jo, Staniszewska, Sophie, Simera, Iveta, Seers, Kate, Mockford, Carole, Goodlad, Susan, Altman, Doug, Moher, David, Barber, Rosemary, Denegri, Simon, Entwistle, Andrew Robert, Littlejohns, Peter, Morris, Christopher, Suleman, Rashida, Thomas, Victoria, Tysall, Colin, 2017. Reaching consensus on reporting patient and public involvement (PPI) in research : methods and lessons learned from the development of reporting guidelines. BMJ Open, 7 (10)
- Haywood, Kirstie L., Brett, Jo, Tutton, Elizabeth, Staniszewska, Sophie, 2017. Patient-reported outcome measures in older people with hip fracture : a systematic review of quality and acceptability. Quality of Life Research, 26 (4), pp. 799-812
- Staniszewska, Sophie, Brett, Jo, Simera, I., Seers, Kate, Mockford, Carole, Goodlad, S., Altman, D. G., Moher, David, Barber, R., Denegri, S., Entwistle, A., Littlejohns, P., Morris, C., Suleman, Rashida, Thomas, V., Tysall, C., 2017. GRIPP2 reporting checklists : tools to improve reporting of patient and public involvement in research. Research Involvement and Engagement, 3 (13)
- Haywood, Kirstie L., Brett, Jo, Salek, Sam, Marlett, Nancy, Penman, Colin, Shklarov, Svetlana, Norris, Colleen, Santana, Maria Jose, Staniszewska, Sophie, 2015. Patient and public engagement in health-related quality of life and patient-reported outcomes research : what is important and why should we care? Findings from the first ISOQOL patient engagement symposium.. Quality of Life Research, 24 (5), pp. 1069-76
- Staniszewska, Sophie, Boardman, Felicity K., Gunn, Lee, Roberts, Julie, Clay, Diane, Seers, Kate, Brett, Jo, Avital, Liz, Bullock, Ian, O' Flynn, N., 2014. The Warwick patient experiences framework : patient-based evidence in clinical guidelines. International Journal for Quality in Health Care, 26 (2), pp. 151-157
- Brett, Jo, Staniszewska, Sophie, Mockford, Carole, Herron-Marx, Sandra, Hughes, John, Tysall, Colin, Suleman, Rashida, 2014. Mapping the impact of patient and public involvement on health and social care research : a systematic review. Health Expectations, 17 (5), pp. 637-650
- Brett, Jo, Staniszewska, Sophie, Mockford, Carole, Herron-Marx, Sandra, Hughes, J. Carl, Tysall, Colin, Suleman, Rashida, 2014. A systematic review of the impact of patient and public involvement on service users, researchers and communities. The Patient - Patient-Centered Outcomes Research, 7 (4), pp. 387-395
- Staniszewska, Sophie, Brett, Jo, Redshaw, Maggie, Hamilton, Karen, Newburn, Mary, Jones, Nicola, Taylor, Lesley, 2012. The POPPY Study : developing a model of family-centred care for neonatal units. Worldviews on Evidence-Based Nursing, Vol.9 (No.4), pp. 243-255
- Staniszewska, Sophie, Haywood, Kirstie L., Brett, Jo, Tutton, Liz, 2012. Patient and public involvement in patient-reported outcome measures. Patient: Patient-Centered Outcomes Research, Vol.5 (No.2), pp. 79-87
- Staniszewska, Sophie, Adebajo, Ade, Barber, Rosemary, Beresford, Peter, Brady, Louca-Mai, Brett, Jo, Elliott, J., Evans, David, Haywood, Kirstie L., Jones, D., Mockford, Carole, Nettle, Mary, Rose, Diana, Williamson, Tracey, 2011. Developing the evidence base of patient and public involvement in health and social care research : the case for measuring impact. International Journal of Consumer Studies, 35 (6), pp. 628-632
- Brett, Jo, Staniszewska, Sophie, Newburn, Mary, Jones, Nicola, Taylor, Lesley, 2011. A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants. BMJ Open, Vol.1 (No.1)
- Staniszewska, Sophie, Brett, Jo, Mockford, Carole, Barber, Rosemary, 2011. The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research. International Journal of Technology Assessment in Health Care, Vol.27 (No.4), pp. 391-399
- Brett, Jo, 2014. Exploring the lived experience of having a hip fracture : identifying patients' perspectives on their health care needs.
- Staniszewska, Sophie, Boardman, Felicity K., Gunn, Lee, Palmer, Julie, Clay, Diane, Seers, Kate, Brett, Jo, 2011. Patient experiences : a scoping study. University of Warwick
- Brett, Jo, Staniszewska, Sophie, Mockford, Carole, Seers, Kate, Herron-Marx, Sandra, Bayliss, Helen, 2010. The PIRICOM study : a systematic review of the conceptualisation, measurement, impact and outcomes of patients and public involvement in health and social care research. University of Warwick
Title | Funder | Award start | Award end |
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PROHIP: Exploring the use of patient-reported outcome measures in the field of hip fractures. | Royal College of Nursing | 01 Sept 2010 | 30 Nov 2012 |