Reflections from a Patient and Carer on Involvement in Research and Integrating Care in the Health System

Reflections from a Patient and Carer on Involvement in Research and Integrating Care in the Health System

Bibliographic Details
Main Authors:	Frank Hanson, Rhene Hanson
Format:	Article
Language:	English
Published:	Ubiquity Press 2017-06-01
Series:	International Journal of Integrated Care
Subjects:	Patient-engagement Caregivers Carers Primary Care Canada Integrated Care
Online Access:	http://www.ijic.org/articles/3088

Similar Items

Supporting young carers: a qualitative review of young carer services in Canada
by: Vivian Stamatopoulos
Published: (2016-04-01)

Measuring the outcomes of long-term care for unpaid carers: comparing the ASCOT-Carer, Carer Experience Scale and EQ-5D-3 L
by: Stacey Rand, et al.
Published: (2019-12-01)

Cultural differences are reflected in variables associated with carer burden in FTD: A comparison study between India and Australia
by: Shailaja Mekala, et al.

“It’s a waiting game” a qualitative study of the experience of carers of patients who require an alternate level of care
by: Kerry Kuluski, et al.
Published: (2017-05-01)

Service user- and carer-reported measures of involvement in mental health care planning: methodological quality and acceptability to users
by: Chris J Gibbons, et al.
Published: (2014-12-01)

Engaging Carers in Co-Design: Development of the Carer Readiness Tool
by: Sian White, et al.
Published: (2021-03-01)

Patients’ engagement in primary care research: a case study in a Canadian context
by: Divya Kanwar Bhati, et al.
Published: (2020-11-01)

“Still learning and evolving in our approaches”: patient and stakeholder engagement among Canadian community-based primary health care researchers
by: Claire Kendall, et al.
Published: (2018-12-01)

Supporting carers: health care professionals in need of system improvements and education - a qualitative study
by: Ingebrigt Røen, et al.
Published: (2019-07-01)

Are Patient and Carer Experiences Mirrored in the Practice Reviews of Self-management Support (PRISMS) Provider Taxonomy?
by: Nicolette Sheridan, et al.
Published: (2017-06-01)

“Never at ease” – family carers within integrated palliative care: a multinational, mixed method study
by: Gülay Ateş, et al.
Published: (2018-03-01)

The impact on carers of individuals with social care needs: the Whole Systems Demonstrator study
by: Michelle Beynon, et al.
Published: (2012-06-01)

The impact on carers of individuals with social care needs: the Whole Systems Demonstrator study
by: Michelle Beynon, et al.
Published: (2012-06-01)

Foster carers' perceptions of planned respite care and the perceived psychosocial effects for foster children.
by: Cooper, Anna Katherine
Published: (2014)

Whose story is it? Mental health consumer and carer views on carer participation in research
by: Alyssa R. Morse, et al.
Published: (2021-05-01)

The awareness, visibility and support for young carers across Europe: a Delphi study
by: Henk Herman Nap, et al.
Published: (2020-10-01)

Are physiotherapists employing person-centred care for people with dementia? An exploratory qualitative study examining the experiences of people with dementia and their carers
by: Abigail J. Hall, et al.
Published: (2018-03-01)

Value and learning from carer involvement in a cluster randomised controlled trial and process evaluation - Organising Support for Carers of Stroke Survivors (OSCARSS)
by: C. Mitchell, et al.
Published: (2020-05-01)

A comparison of strategies to recruit older patients and carers to end-of-life research in primary care
by: Hanratty Barbara, et al.
Published: (2012-09-01)

Carer involvement in compulsory out-patient psychiatric care in England
by: Jorun Rugkåsa, et al.
Published: (2017-11-01)

A comparison of spouse and non-spouse carers of people with dementia: a descriptive analysis of Swedish national survey data
by: Marcus F. Johansson, et al.
Published: (2021-06-01)

Facilitating successful implementation of a person-centred intervention to support family carers within palliative care: a qualitative study of the Carer Support Needs Assessment Tool (CSNAT) intervention
by: J. Diffin, et al.
Published: (2018-12-01)

Family Physician’s and Primary Care Team’s Perspectives on Supporting Family Caregivers in Primary Care Networks
by: Jasneet Parmar, et al.
Published: (2021-03-01)

The Quality of Carer–Patient Relationship Scale: Adaptation and Validation into Portuguese
by: Rosa Silva, et al.
Published: (2021-01-01)

Exploring the Views and Dietary Practices of Older People at Risk of Malnutrition and Their Carers: A Qualitative Study
by: Christina Avgerinou, et al.
Published: (2019-06-01)

Family carers in integrated care: A case study
by: Giovanna Cruz, et al.
Published: (2019-08-01)

Informal Carers Training: In-group Social Learning as an Effective Method for Quality Care Empowerment
by: Jože Ramovš, et al.
Published: (2019-08-01)

Associations between the psychological health of patients and carers in advanced COPD
by: Mi E, et al.
Published: (2017-09-01)

Perceptions of the role of general practice and practical support measures for carers of stroke survivors: a qualitative study
by: Harris Ruth, et al.
Published: (2011-06-01)

The Impact of COVID-19 on the Health and Experience of the Carers of Family Members Living with Dementia: An Italian–Hungarian Comparative Study
by: Almási, V.E, et al.
Published: (2022)

What is important to people with multimorbidity and their caregivers? Identifying attributes of person centred primary health care from the user perspective
by: Kerry Kuluski, et al.
Published: (2019-08-01)

Why are family carers of people with dementia dissatisfied with general hospital care? a qualitative study
by: Jurgens Fiona J, et al.
Published: (2012-09-01)

Mental health service engagement with family and carers: what practices are fundamental?
by: Darryl Maybery, et al.
Published: (2021-10-01)

Motivations for being informal carers of people living with dementia: a systematic review of qualitative literature
by: Nan Greenwood, et al.
Published: (2019-06-01)

Adding to the knowledge on Patient and Public Involvement: Reflections from an experience of co‐research with carers of people with dementia
by: Claudio Di Lorito, et al.
Published: (2020-06-01)

Can eHealth help distance caregivers? A mixed-methods study exploring the use of ICT by carers at a distance in palliative care
by: Carolina Casañas i Comabella
Published: (2014-11-01)

Can eHealth help distance caregivers? A mixed-methods study exploring the use of ICT by carers at a distance in palliative care
by: Carolina Casañas i Comabella
Published: (2014-11-01)

Caregiver Burden and Psychoeducational Interventions in Alzheimer’s Disease: A Review
by: N. Beinart, et al.
Published: (2012-12-01)

User involvement in palliative care: Motivational factors for service users and professionals
by: Sargeant, A., et al.
Published: (2020)

Measuring quality of life in life-threatening illness – content validity and response processes of MQOL-E and QOLLTI-F in Swedish patients and family carers
by: Lena Axelsson, et al.
Published: (2020-03-01)