Teresa Finlay

Datos Biográficos

ID5103100
NOMBRETeresa Finlay
NOMBRESTeresa
APELLIDOFinlay
FIRMAFINLAY T
AFILIACIONESNuffield Department of Primary Care Health Sciences University of Oxford Oxford UK
ORCID0000-0003-2538-8366
VERIFICADOSí
TOTAL DE OBRAS9
TOTAL DE CITAS0
TOTAL COMO AUTOR9
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2017
AÑO MÁS RECIENTE DE PUBLICACIÓN2026
ÍNDICE H0

  • ‘We Are Lost at Sea’

    Open AccessElizabeth C L Jestico, Teresa Finlay et al.ARTICLEQualitative Health Research2026

    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

    Open AccessCaroline Cupit, Teresa Finlay et al.ARTICLESociology of Health & Illness2025

    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

    Open AccessCaroline Cupit, Teresa Finlay et al.ARTICLESocial Science & Medicine2025Referencias: 8

    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

    Open AccessJoanna Crocker, Laëtitia Diez et al.ARTICLEHealth Expectations2024

    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

    Open AccessSonja Erikainen, Phoebe Friesen et al.ARTICLEJournal of Medical Ethics2021

    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

    Open AccessLidewij Eva Vat, Teresa Finlay et al.ARTICLEHealth Expectations2021

    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

    Open AccessLidewij Eva Vat, Teresa Finlay et al.ARTICLEHealth Expectations2020

  • Frameworks for supporting patient and public involvement in research

    Open AccessTrisha Greenhalgh, Lisa Hinton et al.ARTICLEHealth Expectations2019

  • Testing the NHS

    Open AccessTeresa FinlayARTICLENew Genetics and Society2017

    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…