Moving Center Stage: patients claim their role in healthcare

Moving Center Stage: patients claim their role in healthcare

Bibliographic Details
Main Authors:	Anke-Peggy Holtorf, Neil Bertelsen
Format:	Article
Language:	English
Published:	SEEd Medical Publishers 2016-03-01
Series:	Farmeconomia: Health Economics and Therapeutic Pathways
Subjects:	patient centricity patient and public involvement research and development health technology assessment
Online Access:	https://journals.seedmedicalpublishers.com/index.php/FE/article/view/1240

Similar Items

Patient-oriented research competencies in health (PORCH) for researchers, patients, healthcare providers, and decision-makers: results of a scoping review
by: Noreen Frisch, et al.
Published: (2020-02-01)

Research Commentary: A Carer’s Roadmap for Research, Practice, and Policy on Suicide, Homicide, and Self-Harm
by: Anonymous Members of the Peninsula Public Involvement Group, et al.
Published: (2019-05-01)

Development of a standard form for assessing research grant applications from the perspective of patients
by: Maarten de Wit, et al.
Published: (2018-09-01)

Understanding and using patient experiences as evidence in healthcare priority setting
by: Leah Rand, et al.
Published: (2019-09-01)

Engaging indigenous patient partners in patient-oriented research: lessons from a one-year initiative
by: Marie-Claude Tremblay, et al.
Published: (2020-07-01)

“Could you give us an idea on what we are all doing here?” the Patient Voice in Cancer Research (PVCR) starting the journey of involvement in Ireland
by: Éidín Ní Shé, et al.
Published: (2021-09-01)

A Critical Discussion of Patient Engagement in Research
by: Andrea Elaine Bombak, et al.
Published: (2017-01-01)

Public involvement could usefully inform ethical review, but rarely does: what are the implications?
by: Kristina Staley, et al.
Published: (2017-12-01)

Key stakeholders’ views, experiences and expectations of patient and public involvement in healthcare professions’ education: a qualitative study
by: Cadogan, C., et al.
Published: (2022)

Patient and public involvement facilitators: Could they be the key to the NHS quality improvement agenda?
by: Sarah Todd, et al.
Published: (2020-04-01)

Reflections and experiences of a co-researcher involved in a renal research study
by: Sue Marks, et al.
Published: (2018-10-01)

Development and formative evaluation of patient research partner involvement in a multi-disciplinary European translational research project
by: Rebecca Birch, et al.
Published: (2020-02-01)

Co-design of Guidance for Patient and Public Involvement in Psychedelic Research
by: James B. Close, et al.
Published: (2021-09-01)

Involving service users in the qualitative analysis of patient narratives to support healthcare quality improvement
by: Louise Locock, et al.
Published: (2019-01-01)

Patient-Oriented Research Competencies in Health (PORCH) for patients, healthcare providers, decision-makers and researchers: protocol of a scoping review
by: Anastasia A. Mallidou, et al.
Published: (2018-07-01)

“Hitting the spot”: Developing individuals with lived-experience of health and social care as facilitators to deliver a course to enhance public involvement in research – a Welsh perspective
by: Alan Meudell, et al.
Published: (2017-04-01)

The burden of proof: The process of involving young people in research
by: Gail Dovey‐Pearce, et al.
Published: (2019-06-01)

Patient-partner engagement at the Centre de recherche du CHUS in the Province of Québec, Canada: from an intuitive methodology to outreach after three years of implementation
by: Denis Boutin, et al.
Published: (2021-03-01)

Addressing inequities in maternal health among women living in communities of social disadvantage and ethnic diversity
by: Cristina Fernandez Turienzo, et al.
Published: (2021-01-01)

Who should I involve in my research and why? Patients, carers or the public?
by: Kristina Staley, et al.
Published: (2021-06-01)

The impact of public involvement in health research: what are we measuring? Why are we measuring it? Should we stop measuring it?
by: Jill Russell, et al.
Published: (2020-10-01)

Patient Preference Studies During Early Drug Development: Aligning Stakeholders to Ensure Development Plans Meet Patient Needs
by: Nigel S. Cook, et al.
Published: (2019-04-01)

Patient knowledge, experiences and preferences regarding retinoblastoma and research: A qualitative study
by: Catherine Moses, et al.
Published: (2020-06-01)

Co-creating a patient and public involvement and engagement ‘how to’ guide for researchers
by: Raphaela E. Kaisler, et al.
Published: (2020-06-01)

Patient involvement in cardiovascular research: a qualitative impact evaluation
by: Eva Vroonland, et al.
Published: (2019-10-01)

How to engage patient partners in health service research: a scoping review protocol
by: Sarah Cecilie Tscherning, et al.
Published: (2021-04-01)

Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological Diseases
by: Annemarie E. M. Post, et al.
Published: (2021-03-01)

How is knowledge shared in Public involvement? A qualitative study of involvement in a health technology assessment
by: Emma J. Cockcroft, et al.
Published: (2020-04-01)

Participatory action research to pilot a model of mental health service user involvement in an Ethiopian rural primary healthcare setting: study protocol
by: Sisay Abayneh, et al.
Published: (2020-01-01)

EUPATI Guidance for Patient Involvement in Medicines Research and Development: Health Technology Assessment
by: Amy Hunter, et al.
Published: (2018-09-01)

PPI in research: a reflection from early stage researchers
by: Alice M. Biggane, et al.
Published: (2019-11-01)

Patient involvement in healthcare professional practice – a question about knowledge
by: Tine Aagaard
Published: (2017-01-01)

Recruiting patients as partners in health research: a qualitative descriptive study
by: Lidewij Eva Vat, et al.
Published: (2017-08-01)

Long‐term consumer involvement in cancer research: Working towards partnership
by: Kristi Milley, et al.
Published: (2021-08-01)

Patient and public involvement in research: from tokenistic box ticking to valued team members
by: Tracy Jackson, et al.
Published: (2020-04-01)

Patient and public involvement in doctoral research: reflections and experiences of the PPI contributors and researcher
by: Shoba Dawson, et al.
Published: (2020-05-01)

Inverting the patient involvement paradigm: defining patient led research
by: Laura B. Mader, et al.
Published: (2018-07-01)

Conceptualising and constructing ‘diversity’ through experiences of public and patient involvement in health research
by: Joanna Reynolds, et al.
Published: (2021-07-01)

The Canadian retinoblastoma research advisory board: a framework for patient engagement
by: Maxwell J. Gelkopf, et al.
Published: (2020-02-01)

The role of patient and public involvement leads in facilitating feedback: “invisible work”
by: Elspeth Mathie, et al.
Published: (2020-07-01)