Sue Ziebland
#132,017
Most Influential Person Now
Professor of Medical Sociology at the University of Oxford; Director of the Health Experiences Research Group
Sue Ziebland's AcademicInfluence.com Rankings
Sue Zieblandmedical Degrees
Medical
#2215
World Rank
#2621
Historical Rank
Public Health
#325
World Rank
#337
Historical Rank

Download Badge
Medical
Why Is Sue Ziebland Influential?
(Suggest an Edit or Addition)Sue Ziebland's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Analysing qualitative data (2000) (7075)
- Stigma, shame, and blame experienced by patients with lung cancer: qualitative study (2004) (727)
- Making sense of qualitative data analysis: an introduction with illustrations from DIPEx (personal experiences of health and illness) (2006) (556)
- Effects of fruit and vegetable consumption on plasma antioxidant concentrations and blood pressure: a randomised controlled trial (2002) (518)
- How the internet affects patients' experience of cancer: a qualitative study (2004) (492)
- Health and Illness in a Connected World: How Might Sharing Experiences on the Internet Affect People's Health? (2012) (435)
- Men's accounts of depression: reconstructing or resisting hegemonic masculinity? (2006) (416)
- Collecting data on patient experience is not enough: they must be used to improve care (2014) (334)
- Gender, cancer experience and internet use: a comparative keyword analysis of interviews and online cancer support groups. (2006) (314)
- What do patients with prostate or breast cancer want from an Internet site? A qualitative study of information needs. (2004) (284)
- An open letter to The BMJ editors on qualitative research. (2016) (276)
- Effectiveness of health checks conducted by nurses in primary care: final results of the OXCHECK study (1995) (270)
- Prostate cancer: embodied experience and perceptions of masculinity (2002) (270)
- qualitative data Qualitative research in health care : Analysing (1999) (241)
- The importance of being expert: the quest for cancer information on the Internet. (2004) (234)
- Advanced provision of emergency contraception does not reduce abortion rates. (2004) (173)
- Database of patients' experiences (DIPEx): a multi-media approach to sharing experiences and information (2000) (142)
- What affects the uptake of screening for bowel cancer using a faecal occult blood test (FOBt): a qualitative study. (2008) (131)
- Have men been overlooked? A comparison of young men and women's experiences of chemotherapy‐induced alopecia (2008) (130)
- Development and validation of the Day in the Life Questionnaire (DILQ) as a measure of fruit and vegetable questionnaire for 7-9 year olds. (2002) (128)
- Core outcome sets in women's and newborn health: a systematic review (2017) (126)
- Biographical disruption, abruption and repair in the context of motor neurone disease. (2009) (119)
- How information about other people's personal experiences can help with healthcare decision-making: a qualitative study. (2011) (119)
- “The Old Me Could Never Have Done That”: How People Give Meaning to Recovery Following Depression (2006) (116)
- Advancing gender equality through the Athena SWAN Charter for Women in Science: an exploratory study of women’s and men’s perceptions (2017) (114)
- Infertility; isolation and the Internet: a qualitative interview study. (2010) (110)
- Factors contributing to the time taken to consult with symptoms of lung cancer: a cross-sectional study (2008) (110)
- Is ‘watchful waiting’ a real choice for men with prostate cancer? A qualitative study (2002) (108)
- Testing accelerated experience-based co-design: a qualitative study of using a national archive of patient experience narrative interviews to promote rapid patient-centred service improvement (2014) (108)
- Breast cancer in the family—children's perceptions of their mother's cancer and its initial treatment: qualitative study (2006) (106)
- Fertility issues: the perceptions and experiences of young men recently diagnosed and treated for cancer. (2007) (105)
- Desire for the body normal: body image and discrepancies between self reported and measured height and weight in a British population. (1996) (105)
- Importance of sensitivity to change as a criterion for selecting health status measures. (1992) (104)
- Disclosing a Cancer Diagnosis to Friends and Family: A Gendered Analysis of Young Men's and Women's Experiences (2009) (102)
- A comparison of the sensitivity to change of several health status instruments in rheumatoid arthritis. (1993) (98)
- Expressions of Loss of Adulthood in the Narratives of People with Colorectal Cancer (2004) (98)
- Minimizing delays in ovarian cancer diagnosis: an expansion of Andersen's model of 'total patient delay'. (2006) (98)
- Reported barriers to eating more fruit and vegetables before and after participation in a randomized controlled trial: a qualitative study. (2004) (98)
- ‘Getting through’ not ‘going under’: A qualitative study of gender and spousal support after diagnosis with colorectal cancer☆ (2009) (97)
- Qualitative study of men's perceptions of why treatment delays occur in the UK for those with testicular cancer. (2004) (97)
- Exploring men's and women's experiences of depression and engagement with health professionals: more similarities than differences? A qualitative interview study (2007) (96)
- Using alternatives to face-to-face consultations: a survey of prevalence and attitudes in general practice. (2016) (95)
- Comparison of two approaches to measuring change in health status in rheumatoid arthritis: the Health Assessment Questionnaire (HAQ) and modified HAQ. (1992) (94)
- Computer support for recording and interpreting family histories of breast and ovarian cancer in primary care (RAGs): qualitative evaluation with simulated patients (1999) (92)
- Using secondary analysis of qualitative data of patient experiences of health care to inform health services research and policy (2014) (89)
- Personal identity and the role of ‘carer’ among relatives and friends of people with multiple sclerosis☆ (2013) (87)
- Talk of frustration in the narratives of people with chronic pain (2012) (86)
- Using a national archive of patient experience narratives to promote local patient-centered quality improvement: an ethnographic process evaluation of ‘accelerated’ experience-based co-design (2014) (84)
- What people close to death say about euthanasia and assisted suicide: a qualitative study (2006) (82)
- The Role of Humor for Men with Testicular Cancer (2004) (82)
- How patients' experiences contribute to decision making: illustrations from DIPEx (personal experiences of health and illness). (2008) (80)
- Communication with children and adolescents about the diagnosis of a life-threatening condition in their parent (2019) (79)
- Does it matter if clinicians recruiting for a trial don't understand what the trial is really about? Qualitative study of surgeons' experiences of participation in a pragmatic multi-centre RCT (2007) (78)
- Lack of willpower or lack of wherewithal? "Internal" and "external" barriers to changing diet and exercise in a three year follow-up of participants in a health check. (1998) (78)
- Taboo and the different death? Perceptions of those bereaved by suicide or other traumatic death. (2015) (77)
- Viewing the body after bereavement due to a traumatic death: qualitative study in the UK (2010) (76)
- Communication with children and adolescents about the diagnosis of their own life-threatening condition (2019) (75)
- Breast cancer in young families: a qualitative interview study of fathers and their role and communication with their children following the diagnosis of maternal breast cancer (2009) (72)
- Patients' views of routine hospital follow‐up: a qualitative study of women with breast cancer in remission (1998) (72)
- Ethics and dementia: mapping the literature by bibliometric analysis (2003) (66)
- Understanding and using health experiences: Improving patient care (2013) (59)
- Why men with prostate cancer want wider access to prostate specific antigen testing: qualitative study (2002) (59)
- Transition questions to assess outcomes in rheumatoid arthritis. (1993) (58)
- Alternatives to the face-to-face consultation in general practice: focused ethnographic case study (2018) (58)
- “It can't be very important because it comes and goes”—patients' accounts of intermittent symptoms preceding a pancreatic cancer diagnosis: a qualitative study (2014) (57)
- The Effect of Joint Interviewing on the Performance of Gender (2008) (57)
- Smoking cessation interventions for dental patients--attitudes and reported practices of dentists in the Oxford region (1997) (56)
- How the Internet is changing the experience of bereavement by suicide: A qualitative study in the UK (2011) (55)
- A protocol for developing, disseminating, and implementing a core outcome set for pre-eclampsia. (2016) (54)
- Measuring the effects of online health information for patients: Item generation for an e-health impact questionnaire (2013) (54)
- Measuring the effects of online health information: Scale validation for the e-Health Impact Questionnaire. (2015) (54)
- In the absence of evidence, who chooses? A qualitative study of patients' needs after treatment for colorectal cancer (2004) (53)
- The potential of alternatives to face-to-face consultation in general practice, and the impact on different patient groups: a mixed-methods case study (2018) (52)
- 'My brain couldn't move from planning a birth to planning a funeral': a qualitative study of parents' experiences of decisions after ending a pregnancy for fetal abnormality. (2009) (52)
- Body image and weight change in middle age: a qualitative study (2002) (51)
- Emergency contraception: why can't you give it away? Qualitative findings from an evaluation of advance provision of emergency contraception. (2004) (50)
- A core outcome set for pre‐eclampsia research: an international consensus development study (2020) (49)
- What patients do and their impact on implementation. (2016) (49)
- Emergency contraception: an anomalous position in the family planning repertoire? (1999) (48)
- How personal experiences feature in women's accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality. (2011) (47)
- The short form 36 health status questionnaire: clues from the Oxford region's normative data about its usefulness in measuring health gain in population surveys. (1995) (46)
- The specialist palliative care nurse: a qualitative study of the patients' perspective. (2006) (46)
- Concerns and cautions about prescribing and deregulating emergency contraception: a qualitative study of GPs using telephone interviews. (1998) (46)
- The choice is yours? How women with ovarian cancer make sense of treatment choices. (2006) (45)
- Incurable, invisible and inconclusive: watchful waiting for chronic lymphocytic leukaemia and implications for doctor-patient communication. (2012) (45)
- User-Generated Online Health Content: A Survey of Internet Users in the United Kingdom (2014) (45)
- Face-to-Face Compared With Online Collected Accounts of Health and Illness Experiences: A Scoping Review (2020) (43)
- What happened when Scottish women were given advance supplies of emergency contraception? A survey and qualitative study of women's views and experiences. (2005) (42)
- 'Can I come off the tablets now?' A qualitative analysis of heart failure patients' understanding of their medication. (2006) (42)
- On interviewing people with pets: reflections from qualitative research on people with long-term conditions. (2015) (42)
- What do we need to consider when planning, implementing and researching the use of alternatives to face-to-face consultations in primary healthcare? (2016) (42)
- Why do general practitioners prescribe antibiotics for acute infective conjunctivitis in children? Qualitative interviews with GPs and a questionnaire survey of parents and teachers. (2006) (41)
- An Overview of Self-Administered Health Literacy Instruments (2014) (41)
- Conducting a team-based multi-sited focused ethnography in primary care (2017) (41)
- Tackling poorly selected, collected, and reported outcomes in obstetrics and gynecology research (2019) (41)
- Patients' needs following colorectal cancer diagnosis: where does primary care fit in? (2011) (41)
- Outcome reporting across randomised controlled trials evaluating therapeutic interventions for pre‐eclampsia (2017) (40)
- Lung cancer patients' perceptions of access to financial benefits: a qualitative study. (2004) (39)
- Patients' views of a multimedia resource featuring experiences of rheumatoid arthritis: pilot evaluation of www.healthtalkonline.org (2009) (38)
- Tacit models of disability underlying health status instruments. (1993) (37)
- Barriers to shared decisions in the most serious of cancers: a qualitative study of patients with pancreatic cancer treated in the UK (2015) (36)
- Understanding the role of GPs’ gut feelings in diagnosing cancer in primary care: a systematic review and meta-analysis of existing evidence (2020) (35)
- A generic health status instrument in the assessment of rheumatoid arthritis. (1992) (35)
- The DIPEx Project: Collecting Personal Experiences of Illness and Health Care (2008) (35)
- The role of spirituality and religion for those bereaved due to a traumatic death (2011) (34)
- If social determinants of health are so important, shouldn’t we ask patients about them? (2020) (34)
- Imagined futures: how experiential knowledge of disability affects parents’ decision making about fetal abnormality (2012) (33)
- Communication practices for delivering health behaviour change conversations in primary care: a systematic review and thematic synthesis (2019) (33)
- 'I knew before I was told': Breaches, cues and clues in the diagnostic assemblage. (2016) (31)
- Mapping patients’ experiences from initial symptoms to gout diagnosis: a qualitative exploration (2015) (31)
- Understanding depression through a 'coming out' framework. (2012) (30)
- How people bereaved by suicide perceive newspaper reporting: qualitative study. (2013) (30)
- The role of the Internet for people with chronic pain: examples from the DIPEx International Project (2015) (29)
- Health promotion in schools. (1993) (29)
- 'It's a mega dose of hormones, isn't it?' Why women may be reluctant to use emergency contraception (1996) (29)
- ‘People sometimes react funny if they're not told enough’: women's views about the risks of diagnostic laparoscopy (2002) (29)
- Carers, ethics and dementia: a survey and review of the literature (2002) (28)
- A systematic review of primary outcomes and outcome measure reporting in randomized trials evaluating treatments for pre‐eclampsia (2017) (28)
- A qualitative exploration of the role of primary care in supporting colorectal cancer patients (2012) (28)
- Inadequate safety reporting in pre‐eclampsia trials: a systematic evaluation (2018) (28)
- GPs' understanding and practice of safety netting for potential cancer presentations: a qualitative study in primary care. (2018) (27)
- Asking patients about their treatment. (1993) (27)
- Methodological and Practical Issues in Cross-National Qualitative Research: Lessons From the Literature and a Comparative Study of the Experiences of People Receiving a Diagnosis of Cancer (2018) (27)
- What parents say about disclosing the end of their pregnancy due to fetal abnormality. (2013) (25)
- Does stage of change predict outcome in a primary-care intervention to encourage an increase in fruit and vegetable consumption? (2003) (25)
- A systematic review and thematic synthesis of qualitative studies exploring GPs' and nurses' perspectives on discussing weight with patients with overweight and obesity in primary care (2020) (25)
- Narrative as a resource in accounts of the experience of illness (2005) (24)
- Patients’ initial steps to cancer diagnosis in Denmark, England and Sweden: what can a qualitative, cross-country comparison of narrative interviews tell us about potentially modifiable factors? (2017) (24)
- “Why me? I don’t fit the mould … I am a freak of nature”: a qualitative study of women’s experience of gout (2015) (23)
- “You can't do this, you've arthritis": Exploring the experiences of education and employment of young people with arthritis (2018) (23)
- Patients' perceptions of transrectal prostate biopsy: a qualitative study. (2007) (23)
- Examining the role of patients’ experiences as a resource for choice and decision-making in health care: a creative, interdisciplinary mixed-method study in digital health (2016) (22)
- How do frontline staff use patient experience data for service improvement? Findings from an ethnographic case study evaluation (2020) (22)
- Prescribing antibiotics to ‘at-risk’ children with influenza-like illness in primary care: qualitative study (2016) (21)
- Positive prevention: contemporary issues facing HIV positive people negotiating sex in the UK. (2007) (20)
- Using online patient feedback to improve NHS services: the INQUIRE multimethod study (2019) (20)
- A systematic review of reasons for and against asking patients about their socioeconomic contexts (2019) (20)
- Why Men in the United Kingdom Still Want the Prostate Specific Antigen Test (2008) (20)
- Understanding and using health experiences (2013) (19)
- Randomised feasibility study of a novel experience-based internet intervention to support self-management in chronic asthma (2016) (19)
- What outcomes should researchers select, collect and report in pre‐eclampsia research? A qualitative study exploring the views of women with lived experience of pre‐eclampsia (2019) (19)
- Information for choice: what people need, prefer and use - Report for the National Institute for Health Research Service Delivery and Organisation programme (2010) (18)
- Digital health and technological promise: A sociological enquiry (2022) (18)
- The social dimension of health status measures in rheumatoid arthritis. (1991) (18)
- Mike Bury: Biographical Disruption and Long-Term and Other Health Conditions (2015) (17)
- ‘A Mastectomy for Something That Wasn't Even Truly Invasive Cancer.’ Women's Understandings of Having a Mastectomy for Screen-detected Dcis: A Qualitative Study (2011) (17)
- Do we all agree what “good health care” looks like? Views from those who are “seldom heard” in health research, policy and service improvement (2017) (16)
- The use of patients’ stories by self‐help groups: a survey of voluntary organizations in the UK on the register of the College of Health (2000) (15)
- A 'five-a-day' fruit and vegetable pack for primary school children. Part II: controlled evaluation in two Scottish schools (1998) (15)
- The needs and experiences of services by individuals with long-term progressive neurological conditions, and their carers : a benchmarking study (2010) (15)
- DIPEx: fresh insights for medical practice. (2003) (15)
- General Practitioner's use of online resources during medical visits: managing the boundary between inside and outside the clinic. (2019) (15)
- Understanding how front-line staff use patient experience data for service improvement: an exploratory case study evaluation (2020) (15)
- Reassured or fobbed off? Perspectives on infertility consultations in primary care: a qualitative study. (2012) (15)
- "Not that sort of practice": the views and behaviour of primary care practitioners in a study of advance provision of emergency contraception. (2005) (15)
- Methodological decisions influence the identification of potential core outcomes in studies related to pre‐eclampsia: an analysis informing the development of recommendations for future core outcome set developers (2019) (14)
- Informing the development of NICE (National Institute for Health and Care Excellence) quality standards through secondary analysis of qualitative narrative interviews on patients’ experiences (2014) (14)
- What are the mechanisms that enable the reciprocal involvement of seldom heard groups in health and social care research? A rapid realist review protocol (2018) (14)
- Unintended consequences of online consultations: a qualitative study in UK primary care (2021) (14)
- A proper, fitting explanation? : suicide bereavement and perceptions of the coroner's verdict. (2012) (14)
- How wide is the Goldilocks Zone in your health system? (2018) (13)
- GP-delivered brief weight loss interventions: a cohort study of patient responses and subsequent actions, using conversation analysis in UK primary care (2018) (13)
- Why Listening to Health Care Users Really Matters (2012) (13)
- How important is the smoking status of the woman's partner as a predictor of smoking cessation in pregnancy? A literature review (1998) (12)
- Receptionists’ role in new approaches to consultations in primary care: a focused ethnographic study (2018) (12)
- Power, paradox and pessimism: On the unintended consequences of digital health technologies in primary care. (2021) (11)
- Assessing short term outcome (1992) (11)
- Caring for care: Online feedback in the context of public healthcare services. (2021) (10)
- Challenging Explanations for the lack of Senior Women in Science? Reflections from Successful Women Scientists at an elite British University (2018) (10)
- Emotions and chronic illness (2012) (10)
- Not a ‘proper’ solution? The Gap between Professional Guidelines and Users' Views about the Safety of Using Emergency Contraception (1998) (10)
- Exceptionally good? Positive experiences of NHS care and treatment surprises lymphoma patients: a qualitative interview study (2011) (10)
- Quality improvements of safety-netting guidelines for cancer in UK primary care: insights from a qualitative interview study of GPs. (2019) (10)
- Polyphonic perspectives on health and care: Reflections from two decades of the DIPEx project (2020) (10)
- Drawing on Accounts of Long-Term Urinary Catheter Use (2016) (10)
- An Alarming Prognosis: How People Affected by Pancreatic Cancer Use (and Avoid) Internet Information (2012) (9)
- A joint effort over a period of time: factors affecting use of urate-lowering therapy for long-term treatment of gout (2016) (9)
- Caring as sharing. Negotiating the moral boundaries of receiving care (2019) (8)
- Pain and the Internet: Transforming the Experience? (2018) (8)
- Conversations about FGM in primary care: a realist review on how, why and under what circumstances FGM is discussed in general practice consultations (2021) (8)
- Smoking cessation in pregnancy: What's a man to do? (2001) (8)
- A novel experience-based internet intervention for smoking cessation: feasibility randomised controlled trial (2016) (8)
- Depression at work, authenticity in question: Experiencing, concealing and revealing (2019) (8)
- Standardising definitions for the pre-eclampsia core outcome set: A consensus development study. (2020) (7)
- Proliferation of private online healthcare companies (2016) (7)
- Women's experience of coronary heart disease: why is it different? (2012) (7)
- Challenges of safeguarding via remote consulting during the COVID-19 pandemic: a qualitative interview study (2022) (7)
- How do GPs and patients share the responsibility for cancer safety netting follow-up actions? A qualitative interview study of GPs and patients in Oxfordshire, UK (2019) (7)
- Combining patient talk about internet use during primary care consultations with retrospective accounts. A qualitative analysis of interactional and interview data (2021) (6)
- Discussing weight loss opportunistically and effectively in family practice: a qualitative study of clinical interactions using conversation analysis in UK family practice (2020) (6)
- Cultivating Doctors’ Gut Feeling: Experience, Temporality and Politics of Gut Feelings in Family Medicine (2021) (6)
- GPs’ use of gut feelings when assessing cancer risk: a qualitative study in UK primary care (2020) (6)
- Ethics and dementia: the experience of family carers (2004) (5)
- [DIPEx (Database of Individual Patients Experience of illness): a multimedia proposal to share experiences and information about illnesses between patients and health professionals]. (2003) (5)
- Protocol paper for the ‘Harnessing resources from the internet to maximise outcomes from GP consultations (HaRI)’ study: a mixed qualitative methods study (2018) (5)
- Shifting research culture to address the mismatch between where trials recruit and where populations with the most disease live: a qualitative study (2021) (5)
- Testing Accelerated Experience-Based Co-design: Using a National Archive of Patient Experience Narrative Interviews to Promote Rapid Patient-Centred Service Improvement (2013) (5)
- Are some feasibility studies more feasible than others? A review of the outcomes of feasibility studies on the ISRCTN registry (2021) (5)
- Testing Accelerated Experience-Based Co-design (2013) (5)
- Could a publicity campaign for emergency contraception reduce the incidence of unwanted pregnancy and how would we know if it did (1995) (5)
- Society for Social Medicine annual meeting 2000 (2000) (4)
- Supporting patients with female genital mutilation in primary care: a qualitative study exploring the perspectives of GPs' working in England. (2020) (4)
- The convivial and the pastoral in patient–doctor relationships: a multi‐country study of patient stories of care, choice and medical authority in cancer diagnostic processes (2020) (4)
- Gender in the Consolidated Criteria for Reporting Qualitative Research (COREQ) Checklist. (2021) (4)
- DIPEx: Fresh Insights for Medical Practice (2003) (4)
- An introduction to qualitative methods for health professionals. Master classes in primary care research No. 1. (2000) (3)
- What happens when patients say "no" to offers of referral for weight loss? - Results and recommendations from a conversation analysis of primary care interactions. (2021) (3)
- GPs’ use of gut feelings when assessing cancer risk in primary care: A qualitative study (2020) (3)
- Unintended consequences of patient online access to health records: a qualitative study in UK primary care (2022) (3)
- Narratives of experience of mental health and illness on healthtalk.org (2016) (3)
- Assessing health research grant applications: A retrospective comparative review of a one-stage versus a two-stage application assessment process (2020) (3)
- A 'five-a-day' fruit and vegetable pack for primary school children. Part I : development and pre-testing (1998) (3)
- Qualitative cross-country comparison of whether, when and how people diagnosed with lung cancer talk about cigarette smoking in narrative interviews (2018) (3)
- Understanding the role of General Practitioners’ gut feelings in diagnosing cancer in primary care: A systematic review and meta-analysis of existing evidence (2020) (2)
- Analysis (2019) (2)
- People with weight‐related long‐term conditions want support from GPs: A qualitative interview study (2021) (2)
- Qualitative study: patients’ enduring concerns about discussing internet use in general practice consultations (2021) (2)
- Commentary: What is the best way to promote healthy eating? (2006) (2)
- Process evaluation of a research workshop and follow-up support to help practitioners from 13 weight management projects to carry out evaluations (1999) (2)
- Update on DIPEx: a Database of Individual Patients' Experience (2001) (1)
- Evaluation of sexual health interventions (1995) (1)
- SENSITIVITY TO CHANGE OVER TIME OF 4 HEALTH-STATUS INSTRUMENTS IN RHEUMATOID-ARTHRITIS (1992) (1)
- Primary outcome and outcome measure reporting in randomized trials evaluating treatments for preeclampsia: a systematic review. (2017) (1)
- Connecting worlds: social work educators’ perceptions on the role of lived experience in pedagogic practice (2022) (1)
- The collection of narratives on face mask wearing written by members of scholarly association Navigating Knowledge Landscapes Network in May 2020 (2020) (1)
- 23 Completeness of outcome and outcome measure reporting across seventy-nine randomised trials, 31,615 participants, evaluating therapeutic interventions for pre-eclampsia: A systematic review (2016) (1)
- Information for choice (2010) (1)
- Self-monitoring blood pressure in hypertensive pregnancies: the OPTIMUM-BP pilot randomised-controlled trial (2019) (1)
- Help-seeking behaviour in smokers and ex-smokers with symptoms of lung cancer. The application of an integrated model (2009) (1)
- Nurses should be encouraged and helped to monitor patients' medicines. (2011) (1)
- Talking delicately: Providing opportunistic weight loss advice to people living with obesity (2022) (1)
- Women's Distress about Unexpected Dcis Uncertainties and Information Provision (Response to Pryke et Al.) (2011) (1)
- THE E-HEALTH IMPACT QUESTIONNAIRE: DEVELOPING A TOOL TO MEASURE THE EFFECTS OF USING HEALTH-RELATED WEBSITES (2013) (1)
- Perceptions and experiences of blood pressure self-monitoring during hypertensive pregnancy: A qualitative analysis of women's and clinicians' experiences in the OPTIMUM-BP trial. (2022) (1)
- E-Health: The Advent of Online Cancer Information Systems (2011) (1)
- Developing a pre-eclampsia core outcome set. Round 1 results: 283 healthcare professionals, 41 researchers and 112 patients from 55 countries participated (2017) (1)
- Cultivating doctors’ gut feeling: Temporality, place and politics of gut-feelings in family medicine (2020) (1)
- the face-to-face consultation in (2018) (0)
- Authors’ reply to Soljak, Robson and colleagues, and Kelly (2021) (0)
- POSTER VIEWING SESSION - PSYCHOLOGY AND COUNSELLING (2011) (0)
- Evaluation of sexual health interventions [letter] (1995) (0)
- Extracts reproduced from ‘The Guidelines Manual’ (2014) (0)
- Randomised controlled trial of magnetic bracelets for relieving pain in osteoarthritis of the hip and knee (2004) (0)
- Understanding and Using Patients' Experiences to Improve Health Care (2016) (0)
- The clinical guideline development process (2014) (0)
- Communication with children 1 Communication with children and adolescents about the diagnosis of their own life-threatening condition (2019) (0)
- Cultivating Doctors’ Gut Feeling: Experience, Temporality and Politics of Gut Feelings in Family Medicine (2021) (0)
- Objective 4: to inform the development of measurement tools on patients’ experiences (2014) (0)
- Synthesis and framework for future evaluation (2018) (0)
- Emergency contraception [letter] (1995) (0)
- Exploring the experiences of healthcare professionals in South Africa and Uganda around communicating with children about life-threatening conditions: a workshop-based qualitative study to inform the adaptation of communication frameworks for use in these settings (2023) (0)
- Work package 2b: understanding the important factors for user engagement with online personal experiences (2016) (0)
- Objective 5: development of resources for secondary analysis (2014) (0)
- "It's such an emotional thing" - infertility in primary care; a qualitative study. (2018) (0)
- 289. Self-monitoring BP in hypertensive pregnancies: The OPTIMUM-BP pilot study (2018) (0)
- Plenary Sessions Primary Care Geography the Conundrum of Responsible or Resident Populations (0)
- Measuring the impact of using health-related websites: The eHealth impact questionnaire (2015) (0)
- Patient experience of asthma: initial briefing note for NICE drawing on Health Experiences Research Group qualitative data analysis (2014) (0)
- Developing a web based information resource for young people living with chronic arthritis and their carers (2014) (0)
- Software for Analysing Textual Data (1996) (0)
- Objective 3: knowledge transfer between Health Experiences Research Group and NICE teams (2014) (0)
- Introduction to secondary analysis (2014) (0)
- “A word I use almost every day but actually what does it mean?” An interview study of GPs’ understanding and practice of safety netting for potential cancer presentations. (2018) (0)
- A scoping review and stakeholder consultation charting the current landscape of the evidence on online patient feedback (2019) (0)
- Health inequalities, ethnic minorities and COVID19: interactive theatre workshop drawing on a qualitative interview study (2022) (0)
- Building the case for the use of gut feelings in cancer referrals: perspectives of patients referred to a non-specific symptoms pathway (2021) (0)
- Participants at workshop to inform objective 4 (2014) (0)
- Objective 2: testing the reach of the candidate core components across health-care contexts and social groups (2014) (0)
- Membership of project advisory panel (2014) (0)
- Qualitative research: breaking new ground in medical education (2006) (0)
- The Cambridge guide to infertility management and assisted reproduction.Godwin I Meniru. (289 pages, £32.95, US$47.95.) Cambridge University Press, 2001. ISBN 0-521-01071-3. (2002) (0)
- Young women described the benefits of having advance supplies of emergency contraception but emphasised its use as a ''last resort'' rather than an alternative form of contraception (2006) (0)
- Experiences of infertility: where do men fit in? (2011) (0)
- A database of patient experience: moving beyond anecdote (2015) (0)
- Understanding Telehealth in Heart Failure (2017) (0)
- NICE draft quality standard: asthma (2014) (0)
- Explicit resistance within unsolicited conversations about weight in primary care (2023) (0)
- Dietary effect on blood pressure - Reply (2002) (0)
- Qualitative methods session (2014) (0)
- Work package 1c: refining and validation of the e-Health Impact Questionnaire (2016) (0)
- Qualitative research at the National Clinical Guidelines Centre follow-up survey (2014) (0)
- Society for Social Medicine and the International Epidemiological Association European Group (2001) (0)
- Humour and Illness (2008) (0)
- The GLANCE study: Patients’ and GPs’ views on the use of gut feelings for cancer in primary care (2020) (0)
- Emergency contraception. (2016) (0)
- The Role of the Internet for People with Pancreatic Cancer: a Qualitative Study of an Illness with a Very Poor Prognosis (2011) (0)
- The DIPEx project: A systematic collection of personal illness experiences (2008) (0)
- Delayed prescribing of antibiotics for sore throat did not lead to significant levels of complication or reattendance for prescription (1998) (0)
- Qualitative secondary analysis workshop (2014) (0)
- Developing and pre-testing an item pool relating to the effects of exposure to health websites (2012) (0)
- Objective 1: qualitative secondary analysis to identify common core components of patients’ experiences of the NHS to inform NICE clinical guidelines and quality standards (2014) (0)
- www.dipex.org -Another useful prostate cancer website (2017) (0)
- Dietary effect on blood pressure (2002) (0)
- ‘I Can Be The Me I Want To Be By Taking an Antidepressant Regularly’: People’s Feelings About Taking Antidepressants (2014) (0)
- Health inequalities, ethnic minorities and COVID19: interactive theatre workshop drawing on a qualitative interview study. (2022) (0)
- Work package 3b: the EXPERT study – randomised trial of patient experience-based websites (2016) (0)
- Adaptability and change (2021) (0)
- Health inequalities, ethnic minorities and COVID19: interactive theatre workshop drawing on a qualitative interview study (2022) (0)
- Cross-National Comparisons of Health Experiences (2014) (0)
- Myocardial infarction patients’ perspectives of care: a secondary analysis of qualitative interviews (2014) (0)
- Developing a core outcome set for future pre-eclampsia research: an international consensus development study involving 283 healthcare professionals, 41 researchers and 112 patients from 55 countries (2019) (0)
- Survey of the UK public: internet access demographics (2019) (0)
- How the Internet Is Transforming Health Experiences: Reflections from a Decade of Qualitative Research on Experiences of Cancer, Chronic Illness, Infertility and Bereavement (2013) (0)
- NICE draft quality standard: rheumatoid arthritis (2014) (0)
- Patient experience of rheumatoid arthritis: initial briefing note for NICE drawing on Health Experiences Research Group qualitative data analysis (2014) (0)
- Qualitative studies of the benefits and adverse effects of the availability of cancer information and support on the internet (2011) (0)
- Developing a Web Based Information Resource for Young People Living with Chronic Arthritis and Their Carers – Final Report to Arthritis Research UK, Health Experiences Research Group, University of Oxford (2013) (0)
- Understanding and using health experiences to improve healthcare—examples from the United Kingdom (2018) (0)
- Evaluation data collection tools (2014) (0)
- Patient experience quality standard (2014) (0)
- Focused ethnographic case studies, methodology and description of sites (2018) (0)
- How Might the Internet Help Level Health Inequalities (2014) (0)
- Patients'needsfollowingcolorectal cancerdiagnosis: (2011) (0)
- Information and consent materials approved by Research Ethics Committee (2014) (0)
- Children and young people’s experiences of type 1 diabetes: initial briefing note for NICE drawing on Health Experiences Research Group qualitative data analysis (2014) (0)
- QUALITATIVE METHODS IN HEALTH AND MEDICINE - BLOOR,M, TARABORRELLI,P (1995) (0)
- The effect of team-based capital on quality improvement projects in NHS settings (2020) (0)
- title : What patients do and their impact on implementation process and outcomes during ( and after ) participatory quality improvement projects in English acute hospitals : Reflections from an ethnographic study Author details : (2015) (0)
- Understanding and using health experiences to improve healthcare – UK examples (2017) (0)
- Medical Professionalism in the New Information Age (2011) (0)
- Informing the development of NICE Quality Standards through secondary analysis of qualitative narrative interviews on patients' experiences. (2012) (0)
- Temporal aspects of remission: the experiences of patients diagnosed with lymphoma (2008) (0)
- Developing a tool to measure the effects of using health-related websites (the e-Health Impact Questionnaire) (2013) (0)
This paper list is powered by the following services:
Other Resources About Sue Ziebland
What Schools Are Affiliated With Sue Ziebland?
Sue Ziebland is affiliated with the following schools: