Sue Ziebland

Sue Ziebland's AcademicInfluence.com Rankings

Sue Ziebland

Medical

#2215

World Rank

#2621

Historical Rank

Public Health

#325

World Rank

#337

Historical Rank

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Medical

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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)

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www.phc.ox.ac.uk

What Schools Are Affiliated With Sue Ziebland?

Sue Ziebland is affiliated with the following schools:

University of Oxford