Cargando…

Organising Support for Carers of Stroke Survivors (OSCARSS): a cluster randomised controlled trial with economic evaluation

OBJECTIVE: Investigated clinical effectiveness and cost-effectiveness of a person-centred intervention for informal carers/caregivers of stroke survivors. DESIGN: Pragmatic cluster randomised controlled trial (cRCT) with economic and process evaluation. SETTING: Clusters were services, from a UK vol...

Descripción completa

Detalles Bibliográficos
Autores principales:	Patchwood, Emma, Woodward-Nutt, Kate, Rhodes, Sarah A, Batistatou, Evridiki, Camacho, Elizabeth, Knowles, Sarah, Darley, Sarah, Grande, Gunn, Ewing, Gail, Bowen, Audrey
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2021
Materias:	Patient-Centred Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7805348/ https://www.ncbi.nlm.nih.gov/pubmed/33436463 http://dx.doi.org/10.1136/bmjopen-2020-038777

Ejemplares similares

Organising Support for Carers of Stroke Survivors (OSCARSS): study protocol for a cluster randomised controlled trial, including health economic analysis
por: Patchwood, Emma, et al.
Publicado: (2019)

Challenges implementing a carer support intervention within a national stroke organisation: findings from the process evaluation of the OSCARSS trial
por: Darley, Sarah, et al.
Publicado: (2021)

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

Factors associated with carer psychological and physical health during end-of-life caregiving: an observational analysis of a population-based post-bereavement survey of carers of people with cancer
por: Grande, Gunn, et al.
Publicado: (2021)

Systematic review on the involvement and engagement of patients as advisers for the organisation of organ transplantation services
por: Qu, Zhi, et al.
Publicado: (2023)

Care pathway and organisational features driving patient experience: statistical analysis of large NHS datasets
por: Flott, Kelsey, et al.
Publicado: (2018)

Recruitment of patients, carers and members of the public to advisory boards, groups and panels in public and patient involved health research: a scoping review
por: Gilfoyle, Meghan, et al.
Publicado: (2023)

Guidance from key organisations on exploring, confirming and interpreting subgroup effects of medical treatments: a scoping review
por: Wijn, Stan R W, et al.
Publicado: (2019)

How do healthcare professionals working in accountable care organisations understand patient activation and engagement? Qualitative interviews across two time points
por: Mishra, Manish K, et al.
Publicado: (2018)

Investigation of the degree of organisational influence on patient experience scores in acute medical admission units in all acute hospitals in England using multilevel hierarchical regression modelling
por: Sullivan, Paul, et al.
Publicado: (2017)

Talking numbers: how women and providers use risk scores during and after risk counseling – a qualitative investigation from the NRG Oncology/NSABP DMP-1 study
por: Blakeslee, Sarah B, et al.
Publicado: (2023)

Collaboration between patient organisations and a clinical research sponsor in a rare disease condition: learnings from a community advisory board and best practice for future collaborations
por: Roennow, Annelise, et al.
Publicado: (2020)

So near yet so far: why won’t the UK prescribe medical cannabis?
por: Nutt, David, et al.
Publicado: (2020)

Testing the feasibility and acceptability of using the Nintendo Wii in the home to increase activity levels, vitality and well-being in people with multiple sclerosis (Mii-vitaliSe): protocol for a pilot randomised controlled study
por: Thomas, Sarah, et al.
Publicado: (2014)

A patient cohort on long-term sequelae of sepsis survivors: study protocol of the Mid-German Sepsis Cohort
por: Scherag, André, et al.
Publicado: (2017)

Early interventions for the prevention of post-traumatic stress symptoms in survivors of critical illness: protocol for a systematic review
por: Glaspey, Lindsey J, et al.
Publicado: (2017)

Suitability and acceptability of the Carer Support Needs Assessment Tool (CSNAT) for the assessment of carers of people with MND: a qualitative study
por: Ewing, Gail, et al.
Publicado: (2020)

Collaborative design of a decision aid for stroke survivors with multimorbidity: a qualitative study in the UK engaging key stakeholders
por: Porat, Talya, et al.
Publicado: (2019)

Identifying priority policy issues and health system research questions associated with recovery outcomes for burns survivors in India: a qualitative inquiry
por: Jagnoor, Jagnoor, et al.
Publicado: (2018)

Patient, client, consumer, survivor or other alternatives? A scoping review of preferred terms for labelling individuals who access healthcare across settings
por: Costa, Daniel S J, et al.
Publicado: (2019)

‘Much clearer with pictures’: using community-based participatory research to design and test a Picture Option Grid for underserved patients with breast cancer
por: Durand, Marie-Anne, et al.
Publicado: (2016)

Stoic beliefs and health: development and preliminary validation of the Pathak-Wieten Stoicism Ideology Scale
por: Pathak, Elizabeth B, et al.
Publicado: (2017)

Barriers to accessing cancer services for adults with physical disabilities in England and Wales: an interview-based study
por: Sakellariou, Dikaios, et al.
Publicado: (2019)

PROSPECTIV—a pilot trial of a nurse-led psychoeducational intervention delivered in primary care to prostate cancer survivors: study protocol for a randomised controlled trial
por: Watson, Eila, et al.
Publicado: (2014)

Information resources to aid parental decision-making on when to seek medical care for their acutely sick child: a narrative systematic review
por: Neill, Sarah, et al.
Publicado: (2015)

Stakeholder involvement in care transition planning for older adults and the factors guiding their decision-making: a scoping review
por: Carbone, Sarah, et al.
Publicado: (2022)

Pharmacists’ response to anaphylaxis in the community (PRAC): a randomised, simulated patient study of pharmacist practice
por: Salter, Sandra M, et al.
Publicado: (2014)

Measuring ability to assess claims about treatment effects: the development of the ‘Claim Evaluation Tools’
por: Austvoll-Dahlgren, Astrid, et al.
Publicado: (2017)

Protocol for a pilot and feasibility study evaluating a complex nurse-led patient education intervention to promote cancer patient engagement in healthy lifestyle (O-PHE programme)
por: Bonetti, Loris, et al.
Publicado: (2022)

Protocol for a scoping review exploring the use of patient-reported outcomes in adult social care
por: Hughes, Sarah E, et al.
Publicado: (2021)

Decision aids for female BRCA mutation carriers: a scoping review protocol
por: McGarrigle, Sarah A, et al.
Publicado: (2021)

Feasibility study to assess the impact of a lifestyle intervention (‘LivingWELL’) in people having an assessment of their family history of colorectal or breast cancer
por: Anderson, Annie S, et al.
Publicado: (2018)

Quality of care from the perspective of people obtaining abortion: a qualitative study in four countries
por: Baum, Sarah E, et al.
Publicado: (2023)

Patients as partners in Enhanced Recovery After Surgery: A qualitative patient-led study
por: Gillis, Chelsia, et al.
Publicado: (2017)

Strategies and impacts of patient and family engagement in collaborative mental healthcare: protocol for a systematic and realist review
por: Menear, Matthew, et al.
Publicado: (2016)

The Scleroderma Patient-centered Intervention Network (SPIN) Cohort: protocol for a cohort multiple randomised controlled trial (cmRCT) design to support trials of psychosocial and rehabilitation interventions in a rare disease context
por: Kwakkenbos, Linda, et al.
Publicado: (2013)

Families’ healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study
por: Chow, Andrea J, et al.
Publicado: (2022)

Factors influencing practitioner adoption of carer-led assessment in palliative homecare: A qualitative study of the use of the Carer Support Needs Assessment Tool (CSNAT)
por: Austin, Lynn, et al.
Publicado: (2017)

Protocol for the Northern Manhattan Diabetes Community Outreach Project. A randomised trial of a community health worker intervention to improve diabetes care in Hispanic adults
por: Palmas, Walter, et al.
Publicado: (2012)

The tip of an iceberg? A cross-sectional study of the general public's experiences of reporting healthcare complaints in Stockholm, Sweden
por: Wessel, Maja, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_60lcg3jcqn10bobomsj0eis6h7