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Found 29 results.

Searching for: Articles published in 2019

“About sixty per cent I want to do it”: Health researchers’ attitudes to, and experiences of, patient and public involvement (PPI)—A qualitative interview study.

Anne‐Marie Boylan , Louise Locock, Richard Thompson, Sophie Staniszewska.
Health Expectations Epub ahead of print doi.org/10.1111/hex.12883
Added: 27 April 2019

“Power to the people”: the need for more public involvement in Sports Science for Health.

Emma Cockcroft.
Sport Sciences for Health Epub ahead of print, doi.org/10.1007/s11332-019-00548-y
Added: 27 April 2019

Coming from two different worlds—A qualitative, exploratory study of the collaboration between patient representatives and researchers.

Susanne Stuhlfauth, Ingrid Ruud Knutsen, Christina Foss.
Health Expectations ePub ahead of print DOI: 10.1111/hex.12875
Added: 09 April 2019

Consensus Statement on Public Involvement and Engagement with Data-Intensive Health Research.

Mhairi Aitken, Mary P Tully, Carol Porteous, Simon Denegri, Sarah Cunningham-Burley, Natalie Banner, Corri Black, Michael Burgess, Lynsey Cross, Johannes van Delden ,Elizabeth Ford, Sarah Fox, Natalie Fitzpatrick, Kay Gallacher, Catharine Goddard, Lamiece Hassan, Ron Jamieson, Kerina H Jones, Minna Kaarakainen, Fiona Lugg-Widger, Kimberlyn McGrail, Anne McKenzie, Rosalyn Moran, Madeleine J Murtagh, Malcolm Oswald, Alison Paprica, Nicola Perrin, Emma Victoria Richards, John Rouse, Joanne Webb, Donald J Willison.
International Journal of Population Data Science, 4:1:06
Added: 18 March 2019

Engaging patients and caregivers in establishing research priorities for aortic dissection.

Stefan Acosta, Christine Kumlien, Anna Forsberg, Johan Nilsson, Richard Ingemansson, Anders Gottsäter.
SAGE Open Medicine, 7: 1-7.
Added: 29 January 2019

Integrating Parents in Neonatal and Pediatric Research.

Janvier A, Bourque C.J, Dahan S, Robson K, Barrington K.J. on behalf of the Partenariat Famille (PAF) team.
Neonatology, 115:283–291
Added: 08 April 2019

Involving people living with dementia in research: an accessible modified Delphi survey for core outcome set development.

Hazel Morbey, Andrew J. E. Harding, Caroline Swarbrick, Faraz Ahmed, Ruth Elvish, John Keady, Paula R. Williamson and Siobhan T. Reilly.
Trials, 20:12.
Added: 18 February 2019

Involving service users in the qualitative analysis of patient narratives to support healthcare quality improvement.

Louise Locock, Susan Kirkpatrick, Lucy Brading, Gordon Sturmey, Jocelyn Cornwell, Neil Churchill and Glenn Robert.
Research Involvement and Engagement 5:1
Added: 15 February 2019