Buchumschlag

Partnering With Patients to Conduct High‐Quality Research – Where Have We Been and Where Are We Going?

Fuente: Wiley Open Access

Gespeichert in:

Bibliographische Detailangaben
Hauptverfasser:	Daniel Whibley, Greg Merritt, Megan Haymart, Patricia Piechowski, Knoll Larkin, David Williams
Format:	Artículo Open Access
Veröffentlicht:	Wiley 2025
Schlagworte:	Health Expectations
Online-Zugang:	Acceder al recurso
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge

A Qualitative Study to Improve How We Partner With Patients and Families in Healthcare Improvement Collaboratives
von: Cassandra B. Iroz, et al.
Veröffentlicht: (2025)

‘We Don't Have to Prove to People How We're Feeling’: Understanding the Role of Peer Support Groups in Countering Epistemic Injustices in Long COVID at a US Centre
von: Nandini Sarma, et al.
Veröffentlicht: (2025)

‘I Have Never Been in That Kind of All‐Consuming Pain … I Did Not Know What Else to Do’: The Journey to Hospital Admission With Low Back Pain From the Perspectives of Patients
von: Joseph F. Orlando, et al.
Veröffentlicht: (2025)

Young Spouses' Experiences of Having a Partner With Heart Disease and Adolescents Living at Home
von: Matilda Holmbom, et al.
Veröffentlicht: (2024)

How Has ‘What Matters to You’ Been Used for Patient Care? A Scoping Review
von: Carrie Janerka, et al.
Veröffentlicht: (2025)

Training Adolescents and Young Adults to be Partners in Research: Co‐Creating the Young Patients' Autoimmune Research and Empowerment Alliance
von: Anya R. Khurana, et al.
Veröffentlicht: (2026)

Patient Voices: What Can We Learn From the Covid‐19 Pandemic About Follow‐Up Care in Gynaecologic Oncology?
von: Esther M. Vermaas, et al.
Veröffentlicht: (2025)

‘Home Is Where You Are Together’: Qualitative Systematic Review and Meta‐Synthesis of Homeless People's Description of Home
von: Leila Thornhill, et al.
Veröffentlicht: (2026)

What Do We Know About Sharing Power in Co‐Production in Mental Health Research? A Systematic Review and Thematic Synthesis
von: India Hopkins, et al.
Veröffentlicht: (2024)

How Do We Get the Public Into Public Health Research? Learnings and Key Recommendations From Initiating a Community Involvement Project Scheme
von: Carmel McGrath, et al.
Veröffentlicht: (2024)

Establishing Effective Patient Engagement Through a Terms of Reference to Foster Inclusivity and Empowerment in Research: Example From a Healthcare Transition Quality Indicators Project
von: Sarah E. P. Munce, et al.
Veröffentlicht: (2024)

What Can We Learn Four Years On? A Multi‐Centre Service Evaluation Exploring Symptoms, Functional Impact, Recovery and Care Pathways in Long Covid
von: Cassie Lee, et al.
Veröffentlicht: (2025)

Development of a Patient and Carer Advisory Board to Co‐Design Health Services Research for the Quality of Care of People With Dementia
von: Daniel X. Bailey, et al.
Veröffentlicht: (2026)

Evaluation of the Patient Innovation Partner Role: Perceived Benefits, Structures, Supports, and Recommendations for Lived Experience Engagement in Healthcare Innovation Teams
von: Shoshana H. Bardach, et al.
Veröffentlicht: (2025)

Engaging With Health Consumers in Scientific Conferences—As Partners not Bystanders
von: Bronwyn Newman, et al.
Veröffentlicht: (2024)

‘You're Just Thinking About Going Home’: Exploring Person‐Centred Medication Communication With Older Patients at Hospital Discharge
von: Henrik Cam, et al.
Veröffentlicht: (2024)

‘A Forever Imprint on Me…I Couldn't Be There When He Needed Me the Most’: Care Partner Experiences of Patient Safety During Covid‐19 Restrictions
von: Kayley Perfetto, et al.
Veröffentlicht: (2025)

‘We need more support and doctors that understand the process of tapering …’: A content analysis of free‐text responses to a questionnaire on discontinuing long‐term benzodiazepine receptor agonist use
von: Tom Lynch, et al.
Veröffentlicht: (2024)

Patients' and Therapists' Views of Integrated Online CBT for Depression
von: Fiona Fox, et al.
Veröffentlicht: (2024)

Understanding the Needs of Young and Middle‐Aged Chinese People Who Have Experienced a Stroke Who Have Not Successfully Returned to Work: A Qualitative Study
von: Ziwei Liu, et al.
Veröffentlicht: (2025)

A Case Study of Veteran Patient‐Researcher Partnerships in Mental Health Research and Practice: Three Recommendations From a Veteran Patient Engaged in Research (VPER)
von: Madisen E. Brown, et al.
Veröffentlicht: (2025)

Partnering With Youth to Enhance Healthcare Access and Experience: Lessons Learned From a Teen Advisory Group
von: Christi H. Esquivel, et al.
Veröffentlicht: (2025)

Partnering With Teens With Past Suicide‐Related Crises: Development, Application and Refinement of Safety Procedures for Co‐Design
von: Marisa E. Marraccini, et al.
Veröffentlicht: (2026)

Multimodal Analysis of Stories Told by Mental Health Influencers on TikTok
von: Alex Christiansen, et al.
Veröffentlicht: (2025)

‘I Want Everyone to Have It, and Everyone to Be on It’: A Feasibility Study of the Transforming Long Covid Intervention
von: Sarahjane Belton, et al.
Veröffentlicht: (2026)

The Use of Arts‐Based Methods to Enhance Patient Engagement in Health Research
von: Emily K. Phillips, et al.
Veröffentlicht: (2024)

Frameworks to Evaluate the Quality of Public Involvement in Health and Social Care Research: A Scoping Review
von: Rose Hutton, et al.
Veröffentlicht: (2026)

The Supporter Needs Supporting Too: A Qualitative Study to Understand the Maternity Care Experience for Partners Following a Previous Perinatal Death
von: Debbie M. Smith, et al.
Veröffentlicht: (2025)

Challenges and Facilitators to Patient and Public Involvement In Stroke Research: Protocol for a Qualitative Study
von: Hamidreza Khankeh, et al.
Veröffentlicht: (2025)

Co‐Producing Patient‐Reported Experience Measures With People With Intellectual Disability to Improve Healthcare Quality and Outcomes: The ‘Listen to Me’ Project Protocol
von: Reema Harrison, et al.
Veröffentlicht: (2025)

Time for a New Norm: Experiences of ‘Being Informed’ and ‘Having Choice’ for Prenatal Screening for Chromosomal Conditions: A Qualitative Study
von: Niamh Ireland‐Blake, et al.
Veröffentlicht: (2025)

The Importance of Lived Experience: A Scoping Review on the Value of Patient and Public Involvement in Health Research
von: Heather Mah, et al.
Veröffentlicht: (2025)

‘Motivating Implicit Chinese to Express Themselves Is the Biggest Barrier’: A Qualitative Study of Chinese Researchers' Perceptions of Barriers and Facilitators to Patient Engagement in Research
von: Lin Yang, et al.
Veröffentlicht: (2024)

The Lived Experience of Informal Caregivers of People Who Have Severe Mental Illness and Coexisting Long‐Term Conditions: A Qualitative Study
von: C. Carswell, et al.
Veröffentlicht: (2024)

Development of ACT+: A Novel, Person‐Centred Psychological Intervention Based on Acceptance and Commitment Therapy (ACT) to Improve Quality of Life in Patients Living With and Beyond Cancer
von: Elisavet Moschopoulou, et al.
Veröffentlicht: (2025)

Developing, Piloting and Evaluating a Patient Support Portal for Men With Prostate Cancer in Victoria: An Action Research Study
von: Benjamin Shemesh, et al.
Veröffentlicht: (2025)

The Development of Principles for Patient and Public Involvement (PPI) in Preclinical Spinal Cord Research: A Modified Delphi Study
von: Pádraig Carroll, et al.
Veröffentlicht: (2024)

‘Why, Can I Not Have Control of My Own Insulin?’: Qualitative Exploration Amongst Older Adults With Diabetes With Lived Experience of Surgical Hospital Admission
von: Christina Lange Ferreira, et al.
Veröffentlicht: (2025)

Researching Sensitive Topics: The Value of Inclusive Patient and Public Involvement and Engagement in the Design and Implementation of the Larger Bodies in Radiography Project
von: Hancock Amy, et al.
Veröffentlicht: (2026)

Understanding Co‐Creation in a Research Partnership Programme Exploring Patient‐Driven Innovations: A Qualitative Longitudinal Study
von: Hanna Jansson, et al.
Veröffentlicht: (2024)