Copertina

PPIE in a technical research study: Using public involvement to refine the concept and understanding and move towards a multidimensional concept of disability

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autori principali:	William Lammons, Lucky Nobility, Sarah Markham, Eirini‐Christina Saloniki
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2024
Soggetti:	Health Expectations
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

Perspectives of researchers and clinicians on patient and public involvement (PPI) in preclinical spinal cord research: An interview study
di: Pádraig Carroll, et al.
Pubblicazione: (2024)

Patient and public involvement and engagement with underserved communities in dementia research: Reporting on a partnership to co‐design a website for postdiagnostic dementia support
di: Claudio Di Lorito, et al.
Pubblicazione: (2024)

What really is nontokenistic fully inclusive patient and public involvement/engagement in research?
di: Andrea Hilton, et al.
Pubblicazione: (2024)

A rapid review of guidelines on the involvement of adolescents in health research
di: Azza Warraitch, et al.
Pubblicazione: (2024)

‘It's Powerful’ The impact of involving children and young people in developing paediatric research agendas: A qualitative interview study
di: Laura Postma, et al.
Pubblicazione: (2024)

An umbrella review of reviews on challenges to meaningful adolescent involvement in health research
di: Azza Warraitch, et al.
Pubblicazione: (2024)

#DryByChristmas: A patient and public involvement study on women's engagement with humorous pelvic floor muscle training digital nudges on social media
di: Rosie C. Harper, et al.
Pubblicazione: (2024)

Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people
di: Rhiannon Barker, et al.
Pubblicazione: (2024)

Patient and public involvement in the development of health services: Engagement of underserved populations in a quality improvement programme for inflammatory bowel disease using a community‐based participatory approach
di: Elena Sheldon, et al.
Pubblicazione: (2024)

A qualitative study assessing allied health provider perceptions of telepractice functionality in therapy delivery for people with disability
di: Cloe Benz, et al.
Pubblicazione: (2024)

Towards understanding and improving medication safety for patients with mental illness in primary care: A multimethod study
di: Matthew J. Ayre, et al.
Pubblicazione: (2024)

‘The burden is very much on yourself’: A qualitative study to understand the illness and treatment burden of hearing loss across the life course
di: Sian K. Smith, et al.
Pubblicazione: (2024)

Institutional Abuse, Neglect and Harm in UK Community Mental Health Services: A Scoping Review of the Peer‐Reviewed Evidence
di: Bethan M. Edwards, et al.
Pubblicazione: (2025)

A qualitative evaluation of a co‐design process involving young people at risk of suicide
di: Michelle Kehoe, et al.
Pubblicazione: (2024)

What aspects of health and wellbeing are most important to parent carers of children with disabilities?
di: Caomhan McGlinchey, et al.
Pubblicazione: (2024)

Establishing a standing patient advisory board in family practice research: A qualitative evaluation from patients' and researchers' perspectives
di: Jennifer Engler, et al.
Pubblicazione: (2024)

Children's behavioural and emotional reactions towards living with congenital heart disease in Saudi Arabia: A grounded theory study
di: Nada Dahlawi, et al.
Pubblicazione: (2024)

Co‐designing resources to support older people with intellectual disabilities and their families plan for parental death and transitions in care
di: Rebecca Anderson‐Kittow, et al.
Pubblicazione: (2024)

Involvement of children and young people in the conduct of health research: A rapid umbrella review
di: Katherine A. Wyatt, et al.
Pubblicazione: (2024)

Co‐production of health and social science research with vulnerable children and young people: A rapid review
di: Jo Erwin, et al.
Pubblicazione: (2024)

‘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
di: Tom Lynch, et al.
Pubblicazione: (2024)

Accessing care for Long Covid from the perspectives of patients and healthcare practitioners: A qualitative study
di: Fidan Turk, et al.
Pubblicazione: (2024)

Barriers and facilitators to engaging with a digital self‐management programme for painful distal upper limb musculoskeletal disorders: A qualitative exploratory study
di: Samantha J. Mason, et al.
Pubblicazione: (2024)

The Co‐Production, Pilot and Qualitative Evaluation of a Cancer Prevention Programme With High‐Risk Women Delivered on Group Walks by Cancer Champions: Shoulder to Shoulder, Walk and Talk
di: Sarah Hanson, et al.
Pubblicazione: (2024)

Co‐design of the EMBED‐Care Framework as an intervention to enhance shared decision‐making for people affected by dementia and practitioners, comprising holistic assessment, linked with clinical decision support tools: A qualitative study
di: Jesutofunmi Aworinde, et al.
Pubblicazione: (2024)

Navigating HOPE (Hypermobile Online Pain managemEnt): Perspectives and Experiences From People With Hypermobile Ehlers–Danlos Syndrome or Hypermobility Spectrum Disorder on a Condition‐Specific Online Pain Management Programme
di: Min Tze Chew, et al.
Pubblicazione: (2025)

A systematic review of theories, models and frameworks used for youth engagement in health research
di: Sherald Sanchez, et al.
Pubblicazione: (2024)

Lived Experience Participation in Suicide Prevention Activities in Australia, a Scoping Review
di: Hayley Purdon, et al.
Pubblicazione: (2025)

Co‐production and adaptation of a prison‐based problem‐solving workbook to support the mental health of patients housed within a medium‐ and low‐secure forensic service
di: Amanda E. Perry, et al.
Pubblicazione: (2024)

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

Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey
di: Alexander Chaitoff, et al.
Pubblicazione: (2025)

The process of co‐designing a model of social prescribing: An Australian case study
di: Candice Oster, et al.
Pubblicazione: (2024)

Public Contribution in Qualitative Research With Parents of Children Treated for Cancer: Description of and Reflections on a Collaborative Data Analysis Approach
di: Ella Thiblin, et al.
Pubblicazione: (2026)

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

Co‐Design of a Unified, International Aphasia Awareness Campaign
di: Claire Bennington, et al.
Pubblicazione: (2026)

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

The expectations and experiences of patients regarding the diagnostic workup at a specialized memory clinic: An interview study
di: Malin Aspö, et al.
Pubblicazione: (2024)

The First Nations experience of accessing rheumatology services in a metropolitan hospital: A qualitative study
di: Taylor Cullen, et al.
Pubblicazione: (2024)

Science Shops as key intermediary structures to respond to the current health research agenda bias: Evidence from the InSPIRES project
di: Aina Estany, et al.
Pubblicazione: (2024)

Community views on the secondary use of general practice data: Findings from a mixed‐methods study
di: Annette J. Braunack‐Mayer, et al.
Pubblicazione: (2024)