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Found 39 results.

Searching for: Titles starting with P

Patient and public involvement in doctoral research: Impact, resources and recommendations.

Nia Coupe & Amy Mathieson
Health Expectations, Epub ahead of print, DOI: 10.1111/hex.12976
Added: 19 December 2019

Public involvement in the dissemination of the North West Coast Household Health Survey: Experiences and lessons of co‐producing research together.

Clarissa Giebel, Shaima Hassan, Jason C McIntyre, Rhiannon Corcoran, Ben Barr, Mark Gabbay, Jennifer Downing, Terence Comerford, Ana Alfirevic.
Health Expectations, Epub ahead of print, doi.org/10.1111/hex.12940
Added: 19 December 2019

Public Involvement - why bother? Reflections from a study informing the design of multimedia information resources to improve engagement of children, young people and their families with trials.

Sheridan Rebecca, Preston Jennifer, Stones Simon, Ainsworth Sammy, Horton-Taylor Danielle, Challinor Robyn, Ainsworth S, Martin-Kerry Jacqueline, Brady Louca-Mai, Knapp Peter.
Research for All. ISSN 2399-8121 (In Press)
Added: 12 December 2019

PPI in research: a reflection from early stage researchers.

Alice M. Biggane, Maria Olsen & Paula R. Williamson.
Research Involvement and Engagement volume 5, Article number: 35
Added: 10 December 2019

Patient involvement in cardiovascular research: a qualitative impact evaluation.

Eva Vroonland, Inge Schalkers, Daphne Bloemkolk & Christine Dedding
Research Involvement and Engagement, 5: 29.
Added: 02 December 2019

Patient and public involvement in designing and conducting doctoral research: the whys and the hows.

Justine Tomlinson, Kristina Medlinskiene, V-Lin Cheong, Sarah Khan & Beth Fylan.
Research Involvement and Engagement volume 5, Article number: 23
Added: 02 December 2019

Principles and strategies for involving patients in research in chronic kidney disease: report from national workshops.

Talia Gutman, Allison Tong, Martin Howell, Kathryn Dansie, Carmel M Hawley, Jonathan C Craig, Shilpanjali Jesudason, Jeremy R Chapman, David W Johnson, Lisa Murphy, Donna Reidlinger, Sally Crowe, Emily Duncanson, Shyamsundar Muthuramalingam, Nicole Scholes-Robertson, Amber Williamson, Stephen McDonald, Better Evidence and Translation in Chronic Kidney Disease (BEAT-CKD) Workshop Investigators
Nephrology Dialysis Transplantation, gfz076,
Added: 28 November 2019

Public involvement in health outcomes research: lessons learnt from the development of the recovering quality of life (ReQoL) measures.

Andrew Grundy, Anju Devianee Keetharuth, Rosemary Barber, Jill Carlton, Janice Connell, Elizabeth Taylor Buck, Michael Barkham, Thomas Ricketts, Dan Robotham, Diana Rose, John Kay, Rob Hanlon and John Brazier.
Health and Quality of Life Outcomes,17:60.
Added: 09 July 2019

Patients as Research Partners; How to Value their Perceptions, Contribution and Labour?

Elise Smith, Jean-Christophe Bélisle-Pipon, David Resnik.
Citizen Science: Theory and Practice, 4(1):15.
Added: 09 April 2019

Practical Guidance for Involving Stakeholders in Health Research.

Concannon TW, Grant S, Welch V, Petkovic J, Selby J, Crowe S, Synnot A, Greer-Smith R, Mayo-Wilson E, Tambor E, Tugwell P; Multi Stakeholder Engagement (MuSE) Consortium.
Journal of General Internal Medicine, 34(3): 458-463.
Added: 08 April 2019