Teresa Finlay
Biographic Data
| ID | 5103100 |
|---|---|
| NAME | Teresa Finlay |
| GIVEN NAMES | Teresa |
| FAMILY NAME | Finlay |
| SIGNATURE | FINLAY T |
| AFFILIATIONS | Nuffield Department of Primary Care Health Sciences University of Oxford Oxford UK |
| ORCID | 0000-0003-2538-8366 |
| VERIFIED | Yes |
| TOTAL WORKS | 9 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 9 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2017 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
‘We Are Lost at Sea’
As parents process the devastating news that their child has been diagnosed with cancer, they enter a world where they are faced with making many complex decisions. Whilst previous research has focused on how healthcare professionals may support parental decision-making, limited attention has been given to how parents may turn to their social support networks for help. This hermeneutic phenomenological study explored what it means for parents to …
Mapping the Social Organisation of Neglect in the Case of Fibromyalgia
Fibromyalgia is a syndrome characterised by persistent unexplained pain and fatigue. People with fibromyalgia report receiving little support to manage symptoms, difficult interactions with healthcare practitioners and stigma associated with this contested condition. In this article, we employ Dorothy E Smith's Sociology for People to undertake a systems‐focused literature review from the standpoint of people with fibromyalgia, moving beyond indi…
Chronicity rhetoric in health and welfare systems inhibits patient recovery
Fibromyalgia is a leading cause of disability in the UK and worldwide, but is difficult to diagnose and treat due to unclear pathogenesis and diverse and fluctuating symptoms. Although various treatment modalities are recommended, no treatments have been proven to effect sustainable improvement or recovery, and patients are typically dissatisfied with their care. Increasingly, biopsychosocial services are being developed, that aim to take a multi…
Overarching Priorities for Health and Care Research in the United Kingdom
Patients or service users and carers were involved throughout the study, including deciding the aims, designing the study, analysing priorities to identify themes, interpreting and reporting the findings
Public involvement in the governance of population-level biomedical research
Population-level biomedical research offers new opportunities to improve population health, but also raises new challenges to traditional systems of research governance and ethical oversight. Partly in response to these challenges, various models of public involvement in research are being introduced. Yet, the ways in which public involvement should meet governance challenges are not well understood. We conducted a qualitative study with 36 exper…
Evaluation of patient engagement in medicine development
BACKGROUND: Patient engagement is becoming more customary in medicine development. However, embedding it in organizational decision-making remains challenging, partly due to lack of agreement on its value and the means to evaluate it. The objective of this project was to develop a monitoring and evaluation framework, with metrics, to demonstrate impact and enhance learning. METHODS: A consortium of five patient groups, 15 biopharmaceutical compan…
Evaluating the “return on patient engagement initiatives” in medicines research and development
Frameworks for supporting patient and public involvement in research
Testing the NHS
This study examines direct-to-consumer genetic testing (DTCGT) in the UK using the Social Construction of Technology framework to draw conclusions about how commercial genotyping is being shaped by principal groups involved with the technology. Different tests are available including single nucleotide polymorphism genotyping for ancestry and health information, the latter being the focus of this study. I conducted interviews with DTCGT users, and…
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Testing the NHS
This study examines direct-to-consumer genetic testing (DTCGT) in the UK using the Social Construction of Technology framework to draw conclusions about how commercial genotyping is being shaped by principal groups involved with the technology. Different tests are available including single nucleotide polymorphism genotyping for ancestry and health information, the latter being the focus of this study. I conducted interviews with DTCGT users, and…
Frameworks for supporting patient and public involvement in research
Evaluating the “return on patient engagement initiatives” in medicines research and development
Public involvement in the governance of population-level biomedical research
Population-level biomedical research offers new opportunities to improve population health, but also raises new challenges to traditional systems of research governance and ethical oversight. Partly in response to these challenges, various models of public involvement in research are being introduced. Yet, the ways in which public involvement should meet governance challenges are not well understood. We conducted a qualitative study with 36 exper…
Evaluation of patient engagement in medicine development
BACKGROUND: Patient engagement is becoming more customary in medicine development. However, embedding it in organizational decision-making remains challenging, partly due to lack of agreement on its value and the means to evaluate it. The objective of this project was to develop a monitoring and evaluation framework, with metrics, to demonstrate impact and enhance learning. METHODS: A consortium of five patient groups, 15 biopharmaceutical compan…
Overarching Priorities for Health and Care Research in the United Kingdom
Patients or service users and carers were involved throughout the study, including deciding the aims, designing the study, analysing priorities to identify themes, interpreting and reporting the findings
Mapping the Social Organisation of Neglect in the Case of Fibromyalgia
Fibromyalgia is a syndrome characterised by persistent unexplained pain and fatigue. People with fibromyalgia report receiving little support to manage symptoms, difficult interactions with healthcare practitioners and stigma associated with this contested condition. In this article, we employ Dorothy E Smith's Sociology for People to undertake a systems‐focused literature review from the standpoint of people with fibromyalgia, moving beyond indi…
Chronicity rhetoric in health and welfare systems inhibits patient recovery
Fibromyalgia is a leading cause of disability in the UK and worldwide, but is difficult to diagnose and treat due to unclear pathogenesis and diverse and fluctuating symptoms. Although various treatment modalities are recommended, no treatments have been proven to effect sustainable improvement or recovery, and patients are typically dissatisfied with their care. Increasingly, biopsychosocial services are being developed, that aim to take a multi…
‘We Are Lost at Sea’
As parents process the devastating news that their child has been diagnosed with cancer, they enter a world where they are faced with making many complex decisions. Whilst previous research has focused on how healthcare professionals may support parental decision-making, limited attention has been given to how parents may turn to their social support networks for help. This hermeneutic phenomenological study explored what it means for parents to …
Medicine (5 works) · Political science (5 works) · Psychology (4 works) · Public relations (4 works) · Sociology (4 works) · Business (3 works) · Computer Science (3 works) · Mental Health and Patient Involvement (3 works) · Biomedical Ethics and Regulation (2 works) · Ethics in Clinical Research (2 works)