J. Brett

发表

Mapping the impact of patient and public involvement on health and social care research: a systematic review

S. Staniszewska, J. Brett, C. Mockford, 2014, Health expectations : an international journal of public participation in health care and health policy.

Developing the evidence base of patient and public involvement in health and social care research

Jim Elliott, Rosemary Barber, Peter Beresford, 2011 .

The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

Rosemary Barber, S. Staniszewska, J. Brett, 2011, International Journal of Technology Assessment in Health Care.

The POPPY study: developing a model of family-centred care for neonatal units.

S. Staniszewska, M. Redshaw, N. Jones, 2012, Worldviews on evidence-based nursing.

A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

Colin Tysall, S. Staniszewska, J. Brett, 2014, The Patient - Patient-Centered Outcomes Research.

A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants

Mary Newburn, S. Staniszewska, N. Jones, 2011, BMJ Open.

Patient-reported outcome measures in older people with hip fracture: a systematic review of quality and acceptability

E. Tutton, S. Staniszewska, J. Brett, 2017, Quality of Life Research.

GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

D. G. Altman, D. Moher, D. Altman, 2017, Research Involvement and Engagement.

GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

D G Altman, P Littlejohns, S Staniszewska, 2017, British Medical Journal.

Patient and Public Involvement in Patient-Reported Outcome Measures

S. Staniszewska, J. Brett, K. Haywood, 2012, The Patient - Patient-Centered Outcomes Research.

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines.

Julie Roberts, Ian Bullock, Kate Seers, 2014, International journal for quality in health care : journal of the International Society for Quality in Health Care.

The PIRICOM study : a systematic review of the conceptualisation, measurement, impact and outcomes of patients and public involvement in health and social care research

Helen R. Bayliss, Kate Seers, K. Seers, 2010 .

What if something goes wrong? A grounded theory study of parents' decision-making processes around mode of breech birth at term gestation.

J. Brett, E. Burns, E. Thompson, 2019, Midwifery.

Exploring the lived experience of having a hip fracture : identifying patients' perspectives on their health care needs

J. Brett, 2014 .

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

S. Staniszewska, C. Norris, M. Santana, 2015, Quality of Life Research.

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

Iveta Simera, David Moher, Colin Tysall, 2017, BMJ Open.