Lista de obras - Sophie Staniszewska - Dominio Público Uruguay

"About sixty per cent I want to do it": Health researchers' attitudes to, and experiences of, patient and public involvement (PPI)-A qualitative interview study

scientific article published on 29 March 2019

'Why does it happen like this?' Consulting with users and providers prior to an evaluation of services for children with life limiting conditions and their families

artículo científico publicado en 2014

A SHARED study-the benefits and costs of setting up a health research study involving lay co-researchers and how we overcame the challenges.

artículo científico publicado en 2016

A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants ⬇️

artículo científico publicado el 2 de junio de 2011

A systematic review of the impact of patient and public involvement on service users, researchers and communities.

artículo científico publicado en 2014

Abstracts from the NIHR INVOLVE Conference 2017: London, UK. 28 November 2017.

artículo científico publicado en 2017

Accessing the user's perspective

artículo científico publicado en 2000

An Open Toolkit for Tracking Open Science Partnership Implementation and Impact

An open toolkit for tracking open science partnership implementation and impact

artículo científico publicado en 2019

An open toolkit for tracking open science partnership implementation and impact.

artículo científico publicado en 2019

Assessing the cost-effectiveness of HPV vaccination strategies for adolescent girls and boys in the UK

artículo científico publicado en 2019

Can we help patients have a better experience? Implementing NICE guidance on patient experience

artículo científico publicado en 2012

Collaborative action around implementation in Collaborations for Leadership in Applied Health Research and Care: towards a programme theory.

artículo científico publicado en 2013

Collective action for implementation: a realist evaluation of organisational collaboration in healthcare ⬇️

artículo científico publicado en 2016

Collective action for knowledge mobilisation: a realist evaluation of the Collaborations for Leadership in Applied Health Research and Care ⬇️

article

Conference report. Current research on nursing workforce issues

artículo científico publicado en 2004

Consumer involvement in health research: a UK scoping and survey

artículo científico publicado en 2014

Developing the infrastructure for patient review in academic journals

article

EVALUATION OF PATIENT AND PUBLIC INVOLVEMENT INITIATIVES IN HEALTH TECHNOLOGY ASSESSMENT: A SURVEY OF INTERNATIONAL AGENCIES.

artículo científico publicado en 2017

Establishing the values for patient engagement (PE) in health-related quality of life (HRQoL) research: an international, multiple-stakeholder perspective.

artículo científico publicado en 2016

Evidence informed decision making: the use of "colloquial evidence" at nice

artículo científico

Experiences of in-patient mental health services: systematic review

scientific article published on 21 March 2019

Frequency of reporting on patient and public involvement (PPI) in research studies published in a general medical journal: a descriptive study.

artículo científico publicado en 2018

Hospital care following emergency admission: a critical incident case study of the experiences of patients with advanced lung cancer and Chronic Obstructive Pulmonary Disease

artículo científico publicado en 2016

How embedded is public involvement in mainstream health research in England a decade after policy implementation? A realist evaluation.

artículo científico publicado en 2018

Identifying features associated with higher-quality hospital care and shorter length of admission for people with dementia: a mixed-methods study

artículo científico publicado en 2020

Impact of advanced autonomous non-medical practitioners in emergency care: protocol for a scoping study

artículo científico publicado en 2017

Implementing health research through academic and clinical partnerships: a realistic evaluation of the Collaborations for Leadership in Applied Health Research and Care (CLAHRC).

artículo científico publicado en 2011

Improving the experience of care for people using NHS services: summary of NICE guidance ⬇️

artículo científico publicado el 16 de marzo de 2012

Mapping the impact of patient and public involvement on health and social care research: a systematic review

artículo científico publicado en 2012

Measuring quality of life in the evaluation of health care

artículo científico publicado el 14 de enero de 1998

Measuring the impact of patient and public involvement: the need for an evidence base

scientific article published on 03 October 2008

Meeting the patient partnership agenda: the challenge for health care workers

scientific article published on 01 February 2004

Meniscal Tear Outcome (METRO) review: a protocol for a systematic review summarising the clinical course and patient experiences of meniscal tears in the current literature

artículo científico publicado en 2020

Meniscal tear outcome Study (METRO Study): a study protocol for a multicentre prospective cohort study exploring the factors which affect outcomes in patients with a meniscal tear

artículo científico publicado en 2020

Moving from rational to normative ideologies of control over public involvement: A case of continued managerial dominance

artículo científico publicado en 2016

Nurses' role in liaising between patients and service providers

artículo científico publicado en 2011

One small step….

artículo científico publicado en 2015

Patient and Public Involvement in research: A journey to co-production

artículo científico publicado en 2021

Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

artículo científico publicado en 2014

Patient and public involvement in patient-reported outcome measures: evolution not revolution.

artículo científico publicado en 2012

Patient and public involvement in research: future challenges

artículo científico publicado en 2013

Patient and public involvement in the implementation of evidence into practice

artículo científico publicado en 2013

Patient expectations and health-related quality of life

artículo científico publicado en 1999

Patient expectations and satisfaction with health care

artículo científico publicado el 21 de enero de 1998

Patients evaluations of their health care: the expression of negative evaluation and the role of adaptive strategies

artículo científico publicado en 2004

Patterns of public participation

artículo científico publicado en 2016

Perspectives on involvement in the peer-review process: surveys of patient and public reviewers at two journals

article

Public involvement in health priority setting: future challenges for policy, research and society.

artículo científico publicado en 2016

Qualitative critical incident study of patients' experiences leading to emergency hospital admission with advanced respiratory illness.

artículo científico publicado en 2016

Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review

artículo científico publicado en 2011

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

artículo científico publicado en 2017

Realist Evaluation of the Use of Patient Experience Data to Improve the Quality of Inpatient Mental Health Care (EURIPIDES) in England: study protocol.

artículo científico publicado en 2018

Recent developments in research at the RCN Institute.

artículo científico publicado en 2004

ReseArch with Patient and Public invOlvement: a RealisT evaluation – the RAPPORT study

Research Involvement and Engagement: reflections so far and future directions.

artículo científico publicado en 2017

Reviewing progress in public involvement in NIHR research: developing and implementing a new vision for the future

Thanks to all those who reviewed for Research Involvement and Engagement in 2015.

artículo científico publicado en 2016

The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research

artículo científico publicado en 2011

The POPPY study: developing a model of family-centred care for neonatal units

artículo científico publicado en 2012

The PRIME project: developing a patient evidence-base

artículo científico publicado en 2010

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines.

artículo científico publicado en 2014

The capacity of health service commissioners to use evidence: a case study

The development of service user-led recommendations for health and social care services on leaving hospital with memory loss or dementia - the SHARED study

artículo científico publicado en 2016

The impact of patient and public involvement on UK NHS health care: a systematic review

artículo científico publicado en 2011

The power of symbolic capital in patient and public involvement in health research

artículo científico publicado en 2016

User involvement in the development of a research bid: barriers, enablers and impacts

artículo científico publicado en 2007

Using PROMs in Healthcare: Who Should Be in the Driving Seat-Policy Makers, Health Professionals, Methodologists or Patients?

artículo científico publicado en 2016

Using patient experience data to support improvements in inpatient mental health care: the EURIPIDES multimethod study

artículo científico publicado en 2020

Lista de obras de Sophie Staniszewska

"About sixty per cent I want to do it": Health researchers' attitudes to, and experiences of, patient and public involvement (PPI)-A qualitative interview study

'Why does it happen like this?' Consulting with users and providers prior to an evaluation of services for children with life limiting conditions and their families

A SHARED study-the benefits and costs of setting up a health research study involving lay co-researchers and how we overcame the challenges.

A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants ⬇️

A systematic review of the impact of patient and public involvement on service users, researchers and communities.

Abstracts from the NIHR INVOLVE Conference 2017: London, UK. 28 November 2017.

Accessing the user's perspective

An Open Toolkit for Tracking Open Science Partnership Implementation and Impact

An open toolkit for tracking open science partnership implementation and impact

An open toolkit for tracking open science partnership implementation and impact.

Assessing the cost-effectiveness of HPV vaccination strategies for adolescent girls and boys in the UK

Can we help patients have a better experience? Implementing NICE guidance on patient experience

Collaborative action around implementation in Collaborations for Leadership in Applied Health Research and Care: towards a programme theory.

Collective action for implementation: a realist evaluation of organisational collaboration in healthcare ⬇️

Collective action for knowledge mobilisation: a realist evaluation of the Collaborations for Leadership in Applied Health Research and Care ⬇️

Conference report. Current research on nursing workforce issues

Consumer involvement in health research: a UK scoping and survey

Developing the infrastructure for patient review in academic journals

EVALUATION OF PATIENT AND PUBLIC INVOLVEMENT INITIATIVES IN HEALTH TECHNOLOGY ASSESSMENT: A SURVEY OF INTERNATIONAL AGENCIES.

Establishing the values for patient engagement (PE) in health-related quality of life (HRQoL) research: an international, multiple-stakeholder perspective.

Evidence informed decision making: the use of "colloquial evidence" at nice

Experiences of in-patient mental health services: systematic review

Frequency of reporting on patient and public involvement (PPI) in research studies published in a general medical journal: a descriptive study.

Hospital care following emergency admission: a critical incident case study of the experiences of patients with advanced lung cancer and Chronic Obstructive Pulmonary Disease

How embedded is public involvement in mainstream health research in England a decade after policy implementation? A realist evaluation.

Identifying features associated with higher-quality hospital care and shorter length of admission for people with dementia: a mixed-methods study

Impact of advanced autonomous non-medical practitioners in emergency care: protocol for a scoping study

Implementing health research through academic and clinical partnerships: a realistic evaluation of the Collaborations for Leadership in Applied Health Research and Care (CLAHRC).

Improving the experience of care for people using NHS services: summary of NICE guidance ⬇️

Mapping the impact of patient and public involvement on health and social care research: a systematic review

Measuring quality of life in the evaluation of health care

Measuring the impact of patient and public involvement: the need for an evidence base

Meeting the patient partnership agenda: the challenge for health care workers

Meniscal Tear Outcome (METRO) review: a protocol for a systematic review summarising the clinical course and patient experiences of meniscal tears in the current literature

Meniscal tear outcome Study (METRO Study): a study protocol for a multicentre prospective cohort study exploring the factors which affect outcomes in patients with a meniscal tear

Moving from rational to normative ideologies of control over public involvement: A case of continued managerial dominance

Nurses' role in liaising between patients and service providers

One small step….

Patient and Public Involvement in research: A journey to co-production

Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium

Patient and public involvement in patient-reported outcome measures: evolution not revolution.

Patient and public involvement in research: future challenges

Patient and public involvement in the implementation of evidence into practice

Patient expectations and health-related quality of life

Patient expectations and satisfaction with health care

Patients evaluations of their health care: the expression of negative evaluation and the role of adaptive strategies

Patterns of public participation

Perspectives on involvement in the peer-review process: surveys of patient and public reviewers at two journals

Public involvement in health priority setting: future challenges for policy, research and society.

Qualitative critical incident study of patients' experiences leading to emergency hospital admission with advanced respiratory illness.

Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

Realist Evaluation of the Use of Patient Experience Data to Improve the Quality of Inpatient Mental Health Care (EURIPIDES) in England: study protocol.

Recent developments in research at the RCN Institute.

ReseArch with Patient and Public invOlvement: a RealisT evaluation – the RAPPORT study

Research Involvement and Engagement: reflections so far and future directions.

Reviewing progress in public involvement in NIHR research: developing and implementing a new vision for the future

Thanks to all those who reviewed for Research Involvement and Engagement in 2015.

The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research

The POPPY study: developing a model of family-centred care for neonatal units

The PRIME project: developing a patient evidence-base

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines.

The capacity of health service commissioners to use evidence: a case study

The development of service user-led recommendations for health and social care services on leaving hospital with memory loss or dementia - the SHARED study

The impact of patient and public involvement on UK NHS health care: a systematic review

The power of symbolic capital in patient and public involvement in health research

User involvement in the development of a research bid: barriers, enablers and impacts

Using PROMs in Healthcare: Who Should Be in the Driving Seat-Policy Makers, Health Professionals, Methodologists or Patients?

Using patient experience data to support improvements in inpatient mental health care: the EURIPIDES multimethod study