Saved in:
| Main Authors: | Elizabeth Remfry, Duncan J. Reynolds, Sylvia Morgado de Queiroz, Social Action for Health, Rohini Mathur, Michael R. Barnes, Alison Thomson |
|---|---|
| Format: | Artículo Open Access |
| Published: |
Wiley
2026
|
| Subjects: | |
| Online Access: | https://onlinelibrary.wiley.com/doi/10.1111/hex.70621 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
Public and Patient Involvement in Artificial Intelligence and Big Data Healthcare Research: An Exploration of Issues and Challenges Within the AI‐Multiply Project
by: Alexandra Thompson, et al.
Published: (2025)
by: Alexandra Thompson, et al.
Published: (2025)
The Importance of Lived Experience: A Scoping Review on the Value of Patient and Public Involvement in Health Research
by: Heather Mah, et al.
Published: (2025)
by: Heather Mah, et al.
Published: (2025)
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study
by: Emma Cockcroft, et al.
Published: (2024)
by: Emma Cockcroft, et al.
Published: (2024)
‘What Do People With Long Covid Want From Healthcare Services?’ A Qualitative Exploration From Lived Experience
by: Clare Rayner, et al.
Published: (2026)
by: Clare Rayner, et al.
Published: (2026)
Protocol for a Field Trial of a Hearing and Vision Support Intervention for People Living in Long‐Term Care in Australia
by: Carly Meyer, et al.
Published: (2025)
by: Carly Meyer, et al.
Published: (2025)
Tools and Resources for Engaging People With Lived and Living Experience and Caregivers in Mental Health and Substance Use Research: Findings From a Survey and Community Consultation Events
by: Lisa D. Hawke, et al.
Published: (2026)
by: Lisa D. Hawke, et al.
Published: (2026)
Improving How Healthcare Staff Support the Psychological Well‐Being of People Living With Post‐Stroke Aphasia: A Co‐Created Study
by: Sarah Northcott, et al.
Published: (2025)
by: Sarah Northcott, et al.
Published: (2025)
Recommendations to Improve Healthcare Service Provision for Cognitive Impairment in People With Parkinson's Disease: A Mixed Methods Study of the Lived Experience Expert Perspective
by: Deepa Sriram, et al.
Published: (2026)
by: Deepa Sriram, et al.
Published: (2026)
The Lived Experience of Informal Caregivers of People Who Have Severe Mental Illness and Coexisting Long‐Term Conditions: A Qualitative Study
by: C. Carswell, et al.
Published: (2024)
by: C. Carswell, et al.
Published: (2024)
‘Beyond the Prescription’: An Arts‐Based Study of Older Adults Living With HIV and Their Primary Care Experiences in Ontario
by: Kristina M. Kokorelias, et al.
Published: (2026)
by: Kristina M. Kokorelias, et al.
Published: (2026)
Four Years in, What Are the Research Priorities for Long COVID? A Research Priority‐Setting Partnership Between People With Lived Experience, Carers, Clinicians and Researchers
by: Aileen Grant, et al.
Published: (2024)
by: Aileen Grant, et al.
Published: (2024)
Exploring Experiences and Designing Guidance for Involving and Engaging Children and Young People in James Lind Alliance Priority Setting Partnerships
by: Laura Postma, et al.
Published: (2025)
by: Laura Postma, et al.
Published: (2025)
Engagement of People With Lived Experience in Spinal Cord Injury to Address Innovation Priorities
by: Julia T. Ross, et al.
Published: (2025)
by: Julia T. Ross, et al.
Published: (2025)
Communities of Practice and Living Labs: A Scoping Review of Principles and Methodologies for Involvement of Lived Experience Experts in Health and Healthcare Research
by: Eliza Watson, et al.
Published: (2026)
by: Eliza Watson, et al.
Published: (2026)
The Challenging Process of Developing an Antenatal Social Intervention for Parents From Culturally Diverse Backgrounds to Reduce Postnatal Distress: A Participatory Action Research Study
by: Sophie Isobel, et al.
Published: (2025)
by: Sophie Isobel, et al.
Published: (2025)
Distributed Health Literacy Among People With Intellectual Disability, Their Supporters and Healthcare Professionals: A Scoping Review
by: Maryann Barrington, et al.
Published: (2026)
by: Maryann Barrington, et al.
Published: (2026)
Understanding Public Judgements on Artificial Intelligence in Healthcare: Dialogue Group Findings From Australia
by: Emma K. Frost, et al.
Published: (2025)
by: Emma K. Frost, et al.
Published: (2025)
Experience, Process, and Impact of Involving Informal Caregivers of People With Dementia as Public Contributors to Inform the Development of a Complex Intervention: A Mixed‐Methods Study
by: Frida Svedin, et al.
Published: (2025)
by: Frida Svedin, et al.
Published: (2025)
Delivering Inclusive Cultural Offers for Social Prescribing: A Realist Evaluation Involving Older People From Global Majority Backgrounds and Cultural Sector Providers in the UK
by: Debra Westlake, et al.
Published: (2026)
by: Debra Westlake, et al.
Published: (2026)
“Convenience, Quickness, and Compassion”: Experiences of People Involved in the Criminal‐Legal System Accessing Medications for Opioid Use Disorder Services From a Mobile Unit in Chicago
by: Toni Martinford, et al.
Published: (2026)
by: Toni Martinford, et al.
Published: (2026)
Side Effects of Psychotropic Medications Experienced by a Community Sample of People Living With Severe and Persistent Mental Illness
by: Jack C. Collins, et al.
Published: (2024)
by: Jack C. Collins, et al.
Published: (2024)
Experiences of Social Relationships for Adults Living With Multiple Long‐Term Conditions: A Qualitative Interview Study
by: Hilda Hounkpatin, et al.
Published: (2025)
by: Hilda Hounkpatin, et al.
Published: (2025)
Barriers and Facilitators to Accessing Preventive Services for Chronic Diseases Among People From Bangladeshi and Nepalese Backgrounds Living in Sydney
by: Afsana Anwar, et al.
Published: (2026)
by: Afsana Anwar, et al.
Published: (2026)
Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams
by: Shoshana H. Bardach, et al.
Published: (2025)
by: Shoshana H. Bardach, et al.
Published: (2025)
Strengthening the Delivery of Physical Healthcare for Adults Living With Serious Mental Illness – A Qualitative Description of Patient and Family Member Perspectives
by: Munazzah Ambreen, et al.
Published: (2025)
by: Munazzah Ambreen, et al.
Published: (2025)
The Heart Health Yarning Tool: Co‐Designing a Shared Decision‐Making Tool With Aboriginal and Torres Strait Islander People for Cardiovascular Disease Prevention and Risk Management
by: Shannon McKinn, et al.
Published: (2025)
by: Shannon McKinn, et al.
Published: (2025)
Co‐Producing Patient‐Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes: The ‘Listen to Me’ Project Protocol
by: Reema Harrison, et al.
Published: (2025)
by: Reema Harrison, et al.
Published: (2025)
Bringing Young People, Health and Social Care Professionals, Transition Champions and Policymakers Together Through Hybrid Methods of Participation: Creating a Space for Shared Understanding of What Is Required to Improve Young People's Healthcare Transition
by: Louise Porter, et al.
Published: (2025)
by: Louise Porter, et al.
Published: (2025)
Exploring the Experiences of Living With the Post‐COVID Syndrome: A Qualitative Study
by: Michail Kalfas, et al.
Published: (2024)
by: Michail Kalfas, et al.
Published: (2024)
Involving Societal Stakeholders in Dementia Risk Reduction: An Explorative Study
by: Jolanda H. M. Dobbe, et al.
Published: (2026)
by: Jolanda H. M. Dobbe, et al.
Published: (2026)
Co‐Design of a Registry‐Based Tailored Follow‐up Service Intervention for People Living With Stroke: A Multiple Method Consensus Approach
by: Tara Purvis, et al.
Published: (2025)
by: Tara Purvis, et al.
Published: (2025)
Codeveloping a Novel Intervention for People With Post‐COVID Condition: The Balance‐ACT Study
by: Lily Felton, et al.
Published: (2025)
by: Lily Felton, et al.
Published: (2025)
The Use of Arts‐Based Methods to Enhance Patient Engagement in Health Research
by: Emily K. Phillips, et al.
Published: (2024)
by: Emily K. Phillips, et al.
Published: (2024)
Outpatient Virtual Care Among People Living With and Beyond Cancer From Culturally and Linguistically Diverse Backgrounds in Australia: A Protocol for a Realist Evaluation
by: Prince Peprah, et al.
Published: (2025)
by: Prince Peprah, et al.
Published: (2025)
Reimagining Dementia Care: A Complex Intervention Systematic Review on Optimising Social Prescribing (SP) for Carers of People Living With Dementia (PLWD) in the United Kingdom
by: Jessica Marshall, et al.
Published: (2025)
by: Jessica Marshall, et al.
Published: (2025)
Supporting Older People Living With Frailty to Self‐Manage Multiple Medicines: An Experience‐Based Co‐Design of a Complex Intervention Developed in UK Primary Care
by: Giorgia Previdoli, et al.
Published: (2025)
by: Giorgia Previdoli, et al.
Published: (2025)
Best Practices Guidelines for the Engagement of People With Lived Experience and Family Members in Mental Health and Substance Use Health Research: A Modified Delphi Consensus Study
by: Lisa D. Hawke, et al.
Published: (2025)
by: Lisa D. Hawke, et al.
Published: (2025)
Personalisation at the Core of Success: Process Evaluation of the LISTEN Randomised Controlled Trial Evaluating a Personalised Self‐Management Support Intervention for People Living With Long Covid
by: Fiona Leggat, et al.
Published: (2025)
by: Fiona Leggat, et al.
Published: (2025)
Establishing Effective Patient Engagement Through a Terms of Reference to Foster Inclusivity and Empowerment in Research: Example From a Healthcare Transition Quality Indicators Project
by: Sarah E. P. Munce, et al.
Published: (2024)
by: Sarah E. P. Munce, et al.
Published: (2024)
Mobilizing the Power of Lived/Living Experiences to Improve Health Outcomes for all
by: Ambreen Sayani, et al.
Published: (2025)
by: Ambreen Sayani, et al.
Published: (2025)
Similar Items
-
Public and Patient Involvement in Artificial Intelligence and Big Data Healthcare Research: An Exploration of Issues and Challenges Within the AI‐Multiply Project
by: Alexandra Thompson, et al.
Published: (2025) -
The Importance of Lived Experience: A Scoping Review on the Value of Patient and Public Involvement in Health Research
by: Heather Mah, et al.
Published: (2025) -
Involving People With Lived Experience in Electronic Health Record Database Studies Reflections and Learning From the CHOOSE Study
by: Emma Cockcroft, et al.
Published: (2024) -
‘What Do People With Long Covid Want From Healthcare Services?’ A Qualitative Exploration From Lived Experience
by: Clare Rayner, et al.
Published: (2026) -
Protocol for a Field Trial of a Hearing and Vision Support Intervention for People Living in Long‐Term Care in Australia
by: Carly Meyer, et al.
Published: (2025)