Patient and Public Involvement in Youth Mental Health Research: Protocol for a Systematic Review of Practices and Impact

par Célia M. D. Sales, Célia M. D. Sales, Filipa Martins, Marisa M. Alves, Sara Carletto, Sonia Conejo-Cerón, Luis Costa da Silva, Luis Costa da Silva, Anja Čuš, Chloe Edridge, Chloe Edridge, Nuno Ferreira, Camellia Hancheva, Esperanca M. A. Lima, Shaun Liverpool, Shaun Liverpool, Nick Midgley, Bettina Moltrecht, Patricia Moreno-Peral, Nicholas Morgan, Rose Mortimer, Catarina Pinheiro Mota, Catarina Pinheiro Mota, Giada Pietrabissa, Giada Pietrabissa, Sonia Sousa, Randi Ulberg, Randi Ulberg, Julian Edbrooke-Childs, Julian Edbrooke-Childs
Publié 2021

Self-Medication for Chronic Pain Using Classic Psychedelics: A Qualitative Investigation to Inform Future Research

par Julia Bornemann, James B. Close, Meg J. Spriggs, Robin Carhart-Harris, Robin Carhart-Harris, Leor Roseman
Publié 2021

“PPI? That sounds like Payment Protection Insurance”: Reflections and learning from a substance use and homelessness study Experts by Experience group

par Rebecca Foster, Hannah Carver, Jason Wallace, Alex Dunedin, Stan Burridge, Philip Foley, Bernie Pauly, Tessa Parkes
Publié 2021

The Place and Importance of Patients in Deliberative Processes

par Marjo S. Cellier
Publié 2021

The mutual benefits of patient and public involvement in research: an example from a feasibility study (MoTaStim-Foot)

par Alison M. Aries, Paul Bailey, Susan M. Hunter
Publié 2021

ReIMAGINE: a prostate cancer research consortium with added value through its patient and public involvement and engagement

par S. Green, S. Tuck, J. Long, T. Green, A. Green, P. Ellis, A. Haire, C. Moss, F. Cahill, N. McCartan, L. Brown, A. Santaolalla, T. Marsden, M. Rodriquez Justo, J. Hadley, S. Punwani, G. Attard, H. Ahmed, C. M. Moore, M. Emberton, M. Van Hemelrijck
Publié 2021

In the works: Patient and public involvement and engagement in healthcare decision‐making

par Bert deGraaff, Tineke Kleinhout‐Vliek, Hester Van de Bovenkamp
Publié 2021

Patient advocacy group involvement in health technology assessments: an observational study

par Ann Single, Ariana Cabrera, Simon Fifer, Jane Tsai, Jin-Young Paik, Philip Hope
Publié 2021

Patients’ experiences in the UK: Future strategic directions

par Sophie Staniszewska, Neil Churchill
Publié 2014

Co-designing new tools for collecting, analysing and presenting patient experience data in NHS services: working in partnership with patients and carers

par Nicola Small, Bie Nio Ong, Annmarie Lewis, Dawn Allen, Nigel Bagshaw, Papreen Nahar, Caroline Sanders, the DEPEND team
Publié 2021

Enabling Transdisciplinary Collaboration: Stakeholder Views on Working With “Children With Mentally Ill Parents” Research Groups

par Raphaela E. Kaisler, Christiane Grill
Publié 2021

Developing a patient-driven chronic obstructive pulmonary disease (COPD) research agenda in the U.S.

par Inga Gruß, Gretchen M. McCreary, Ilya Ivlev, Mary Ellen Houlihan, Barbara P. Yawn, Cara Pasquale, William Clark, Richard A. Mularski
Publié 2021

Conceptual frameworks and degrees of patient engagement in the planning and designing of health services: A scoping review of qualitative studies

par Umair Majid, Anna Gagliardi
Publié 2019

Patient partner compensation in research and health care: the patient perspective on why and how

par Dawn Richards, Isabel Jordan, Kimberly Strain, Zal Press
Publié 2018

Patient and public involvement (PPI) in prisons: the involvement of people living in prison in the research process – a systematic scoping review

par Samantha Treacy, Steven Martin, Nelum Samarutilake, Tine Van Bortel
Publié 2021