Health Expectations

Cover image for Vol. 20 Issue 1

Early View (Online Version of Record published before inclusion in an issue)

Edited By: Carolyn Chew-Graham

Impact Factor: 3.207

ISI Journal Citation Reports © Ranking: 2015: 5/75 (Health Policy & Services); 15/88 (Health Care Sciences & Services); 28/173 (Public Environmental & Occupational Health)

Online ISSN: 1369-7625

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  1. 1 - 66
  1. ORIGINAL RESEARCH PAPERS

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      How lay people understand and make sense of personalized disease risk information

      Olga C. Damman, Nina M. M. Bogaerts, Maaike J. van den Haak and Danielle R. M. Timmermans

      Version of Record online: 17 JAN 2017 | DOI: 10.1111/hex.12538

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      Development and feasibility testing of the Pediatric Emergency Discharge Interaction Coding Scheme

      Janet A. Curran, Alexandra Taylor, Jill Chorney, Stephen Porter, Andrea Murphy, Shannon MacPhee, Andrea Bishop and Rebecca Haworth

      Version of Record online: 12 JAN 2017 | DOI: 10.1111/hex.12512

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      Attending to power differentials: How NP-led group medical visits can influence the management of chronic conditions

      Laura Housden, Annette J. Browne, Sabrina T. Wong and Martin Dawes

      Version of Record online: 10 JAN 2017 | DOI: 10.1111/hex.12525

  2. REVIEW ARTICLES

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      Patient expectations for management of chronic non-cancer pain: A systematic review

      Jose W. Geurts, Paul C. Willems, Craig Lockwood, Maarten van Kleef, Jos Kleijnen and Carmen Dirksen

      Version of Record online: 23 DEC 2016 | DOI: 10.1111/hex.12527

  3. Original Research Papers

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      “Giving us hope”: Parent and neonatal staff views and expectations of a planned family-centred discharge process (Train-to-Home)

      Jenny Ingram, Maggie Redshaw, Sarah Manns, Lucy Beasant, Debbie Johnson, Peter Fleming and David Pontin

      Version of Record online: 21 DEC 2016 | DOI: 10.1111/hex.12514

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      A new graphical format to communicate treatment effects to patients—A web-based randomized controlled trial

      Jürgen Kasper, Adrian van de Roemer, Jana Pöttgen, Anne Rahn, Imke Backhus, Yasemin Bay, Sascha Köpke and Christoph Heesen

      Version of Record online: 16 DEC 2016 | DOI: 10.1111/hex.12522

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      French women's representations and experiences of the post-treatment management of breast cancer and their perception of the general practitioner's role in follow-up care: A qualitative study

      Catherine Laporte, Julie Vaure, Anne Bottet, Bénédicte Eschalier, Mrs Clémentine Raineau, Denis Pezet and Philippe Vorilhon

      Version of Record online: 29 NOV 2016 | DOI: 10.1111/hex.12518

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

      Louise Locock, Anne-Marie Boylan, Rosamund Snow and Sophie Staniszewska

      Version of Record online: 24 NOV 2016 | DOI: 10.1111/hex.12519

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      Communication and patient participation influencing patient recall of treatment discussions

      Claude Richard, Emma Glaser and Marie-Thérèse Lussier

      Version of Record online: 21 NOV 2016 | DOI: 10.1111/hex.12515

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      PReSaFe: A model of barriers and facilitators to patients providing feedback on experiences of safety

      Aoife De Brún, Emily Heavey, Justin Waring, Pamela Dawson and Jason Scott

      Version of Record online: 16 NOV 2016 | DOI: 10.1111/hex.12516

  4. Review Articles

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  5. Original Research Papers

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      “What matters to someone who matters to me”: using media campaigns with young people to prevent interpersonal violence and abuse

      Nicky Stanley, Jane Ellis, Nicola Farrelly, Sandra Hollinghurst, Sue Bailey and Soo Downe

      Version of Record online: 3 NOV 2016 | DOI: 10.1111/hex.12495

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      Similar perspectives on prostate cancer screening value and new guidelines across patient demographic and PSA level subgroups: A qualitative study

      Melissa R. Partin, Sarah E. Lillie, Katie M. White, Timothy J. Wilt, Kristin L. Chrouser, Brent C. Taylor and Diana J. Burgess

      Version of Record online: 2 NOV 2016 | DOI: 10.1111/hex.12517

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      Patient and nurse preferences for implementation of bedside handover: Do they agree? Findings from a discrete choice experiment

      Jennifer A. Whitty, Jean Spinks, Tracey Bucknall, Georgia Tobiano and Wendy Chaboyer

      Version of Record online: 2 NOV 2016 | DOI: 10.1111/hex.12513

  6. Review Articles

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      Is there a role for patients and their relatives in escalating clinical deterioration in hospital? A systematic review

      Abigail K. Albutt, Jane K. O'Hara, Mark T. Conner, Stephen J. Fletcher and Rebecca J. Lawton

      Version of Record online: 26 OCT 2016 | DOI: 10.1111/hex.12496

  7. Original Research Papers

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      Right choice, right time: Evaluation of an online decision aid for youth depression

      Magenta B. Simmons, Aurora Elmes, Joanne E. McKenzie, Lyndal Trevena and Sarah E. Hetrick

      Version of Record online: 17 OCT 2016 | DOI: 10.1111/hex.12510

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      The Partners in Health scale for older adults: design and examination of its psychometric properties in a Dutch population of older adults

      Karin Veldman, Sijmen A. Reijneveld, Maarten M. H. Lahr, Ronald J. Uittenbroek and Klaske Wynia

      Version of Record online: 7 OCT 2016 | DOI: 10.1111/hex.12488

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      Successful participation of patients in interprofessional team meetings: A qualitative study

      Jerôme Jean Jacques van Dongen, Iris Gerarda Josephine Habets, Anna Beurskens and Marloes Amantia van Bokhoven

      Version of Record online: 7 OCT 2016 | DOI: 10.1111/hex.12511

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      What factors influence successful recruitment of siblings of individuals with first episode psychosis to e-health interventions? A qualitative study

      Jacqueline Sin, Claire Henderson, Debbie Spain, Catherine Gamble and Ian Norman

      Version of Record online: 6 OCT 2016 | DOI: 10.1111/hex.12508

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      Content analysis of public opinion on sexual expression and dementia: Implications for nursing home policy development

      Maggie L. Syme, Erin Yelland, Laci Cornelison, Judith L. Poey, Ryan Krajicek and Gayle Doll

      Version of Record online: 5 OCT 2016 | DOI: 10.1111/hex.12509

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      CJCheck Stage 1: development and testing of a checklist for reporting community juries – Delphi process and analysis of studies published in 1996–2015

      Rae Thomas, Rebecca Sims, Chris Degeling, Jackie M. Street, Stacy M. Carter, Lucie Rychetnik, Jennifer A. Whitty, Andrew Wilson, Paul Ward and Paul Glasziou

      Version of Record online: 5 OCT 2016 | DOI: 10.1111/hex.12493

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      Decision making about Pap test use among Korean immigrant women: A qualitative study

      Kyounghae Kim, Soohyun Kim, Joseph J. Gallo, Marie T. Nolan and Hae-Ra Han

      Version of Record online: 30 SEP 2016 | DOI: 10.1111/hex.12507

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      Keeping all options open: Parents’ approaches to advance care planning

      Emma Beecham, Linda Oostendorp, Joanna Crocker, Paula Kelly, Andrew Dinsdale, June Hemsley, Jessica Russell, Louise Jones and Myra Bluebond-Langner

      Version of Record online: 26 SEP 2016 | DOI: 10.1111/hex.12500

  8. Review Articles

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      How best to use and evaluate Patient Information Leaflets given during a consultation: a systematic review of literature reviews

      Mélanie Sustersic, Aurélie Gauchet, Alison Foote and Jean-Luc Bosson

      Version of Record online: 26 SEP 2016 | DOI: 10.1111/hex.12487

  9. Original Research Papers

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      A digital advocate? Reactions of rural people who experience homelessness to the idea of recording clinical encounters

      Stuart W. Grande, Mary Ganger Castaldo, Elizabeth Carpenter-Song, Ida Griesemer and Glyn Elwyn

      Version of Record online: 7 SEP 2016 | DOI: 10.1111/hex.12492

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      Awareness of and reactions to mammography controversy among immigrant women

      Rebekah H. Nagler, Jennifer A. Lueck and Lauren S. Gray

      Version of Record online: 26 AUG 2016 | DOI: 10.1111/hex.12494

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  10. Review Articles

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      Supporting public involvement in interview and other panels: a systematic review

      Susan Baxter, Mark Clowes, Delia Muir, Wendy Baird, Andrea Broadway-Parkinson and Carole Bennett

      Version of Record online: 17 AUG 2016 | DOI: 10.1111/hex.12491

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      How and why should we engage parents as co-researchers in health research? A scoping review of current practices

      Shuoqi Shen, Krissy A.R. Doyle-Thomas, Lori Beesley, Amir Karmali, Laura Williams, Nadia Tanel and Amy C. McPherson

      Version of Record online: 12 AUG 2016 | DOI: 10.1111/hex.12490

  11. Original Research Papers

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      Parents’ concerns about future pregnancy after stillbirth: a qualitative study

      Sarah Meaney, Claire M. Everard, Stephen Gallagher and Keelin O'Donoghue

      Version of Record online: 1 AUG 2016 | DOI: 10.1111/hex.12480

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      Associations between hospital characteristics and patient satisfaction in Germany

      Rike Antje Kraska, Marcel Weigand and Max Geraedts

      Version of Record online: 22 JUL 2016 | DOI: 10.1111/hex.12485

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      Multiple sclerosis patients need and want information on exercise promotion from healthcare providers: a qualitative study

      Yvonne C. Learmonth, Brynn C. Adamson, Julia M. Balto, Chung-yi Chiu, Isabel Molina-Guzman, Marcia Finlayson, Barry J. Riskin and Robert W. Motl

      Version of Record online: 20 JUL 2016 | DOI: 10.1111/hex.12482

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      Understanding of a negative bowel screening result and potential impact on future symptom appraisal and help-seeking behaviour: a focus group study

      Karen N. Barnett, David Weller, Steve Smith, Sheina Orbell, Peter Vedsted, Robert J. C. Steele, Jane W. Melia, Sue M. Moss, Julietta Patnick and Christine Campbell

      Version of Record online: 14 JUL 2016 | DOI: 10.1111/hex.12484

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      Attitudes towards lung cancer screening in socioeconomically deprived and heavy smoking communities: informing screening communication

      Samantha L. Quaife, Laura A. V. Marlow, Andy McEwen, Samuel M. Janes and Jane Wardle

      Version of Record online: 11 JUL 2016 | DOI: 10.1111/hex.12481

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

      Carole Mockford, Kate Seers, Matt Murray, Jan Oyebode, Rosemary Clarke, Sophie Staniszewska, Rashida Suleman, Sue Boex, Yvonne Diment, Richard Grant, Jim Leach and Uma Sharma

      Version of Record online: 8 JUL 2016 | DOI: 10.1111/hex.12477

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      Whose voices? Patient and public involvement in clinical commissioning

      Alison O'Shea, Mary Chambers and Annette Boaz

      Version of Record online: 29 JUN 2016 | DOI: 10.1111/hex.12475

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      Patient involvement in rheumatology outpatient service design and delivery: a case study

      Savia de Souza, James Galloway, Carol Simpson, Radka Chura, Joanne Dobson, Nicola J. Gullick, Sophia Steer and Heidi Lempp

      Version of Record online: 27 JUN 2016 | DOI: 10.1111/hex.12478

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      Public consultation changes guidance on the use of health-care interventions. An observational study

      Bruce Campbell, Jeffrey Tabiri-Essuman, Helen Gallo, Vassilia Verdiel, Lakshmi Mandava, Mohamed Ansaf Azhar and John Powell

      Version of Record online: 17 JUN 2016 | DOI: 10.1111/hex.12476

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      Ordinary risks and accepted fictions: how contrasting and competing priorities work in risk assessment and mental health care planning

      Michael Coffey, Rachel Cohen, Alison Faulkner, Ben Hannigan, Alan Simpson and Sally Barlow

      Version of Record online: 17 JUN 2016 | DOI: 10.1111/hex.12474

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      Necessary but not sufficient? Engaging young people in the development of an avatar-based online intervention designed to provide psychosocial support to young people affected by their own or a family member's cancer diagnosis

      Ceri Phelps, Masoumeh Minou, Andrew Baker, Carol Hughes, Helen French, Wayne Hawkins, Andrew Leeuwenberg, Rebecca Crabtree and Paul B. Hutchings

      Version of Record online: 12 JUN 2016 | DOI: 10.1111/hex.12473

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      Stakeholders in support systems for self-care for chronic illness: the gap between expectations and reality regarding their identity, roles and relationships

      María J. Pumar-Méndez, Agurtzane Mujika, Elena Regaira, Ivaylo Vassilev, Mari Carmen Portillo, Christina Foss, Elka Todorova, Poli Roukova, Ingrid A. Ruud Knutsen, Manuel Serrano, Christos Lionis, Michel Wensing and Anne Rogers

      Version of Record online: 27 MAY 2016 | DOI: 10.1111/hex.12471

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      Elaboration of the Gothenburg model of person-centred care

      Nicky Britten, Lucy Moore, Doris Lydahl, Oncel Naldemirci, Mark Elam and Axel Wolf

      Version of Record online: 18 MAY 2016 | DOI: 10.1111/hex.12468

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      Process and impact of patient involvement in a systematic review of shared decision making in primary care consultations

      Catherine Hyde, Kate M. Dunn, Adele Higginbottom and Carolyn A. Chew-Graham

      Version of Record online: 12 MAY 2016 | DOI: 10.1111/hex.12458

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      Drug breakthrough offers hope to arthritis sufferers: qualitative analysis of medical research in UK newspapers

      Helen Hanson, Nicola O'Brien, Paul Whybrow, John D Isaacs and Tim Rapley

      Version of Record online: 4 MAY 2016 | DOI: 10.1111/hex.12460

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      Doctors’ engagements with patient experience surveys in primary and secondary care: a qualitative study

      Conor Farrington, Jenni Burt, Olga Boiko, John Campbell and Martin Roland

      Version of Record online: 28 APR 2016 | DOI: 10.1111/hex.12465

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      Patients’ use and views of real-time feedback technology in general practice

      Christine Wright, Antoinette Davey, Natasha Elmore, Mary Carter, Luke Mounce, Ed Wilson, Jenni Burt, Martin Roland and John Campbell

      Version of Record online: 28 APR 2016 | DOI: 10.1111/hex.12469

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      Agreeing the content of a patient-reported outcome measure for primary care: a Delphi consensus study

      Mairead Murphy, Sandra Hollinghurst and Chris Salisbury

      Version of Record online: 28 APR 2016 | DOI: 10.1111/hex.12462

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      Defining ‘quality’ from the patient's perspective: findings from focus groups with Medicaid beneficiaries and implications for public reporting

      Ryan P. Theis, Jevetta C. Stanford, J. Robyn Goodman, Lisa L. Duke and Elizabeth A. Shenkman

      Version of Record online: 28 APR 2016 | DOI: 10.1111/hex.12466

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      Communicating with parents of obese children: which channels are most effective?

      Melanie Randle, Anthony D. Okely and Sara Dolnicar

      Version of Record online: 28 APR 2016 | DOI: 10.1111/hex.12463

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      Patient involvement in the development of a handbook for moderate rheumatoid arthritis

      Louise Prothero, Sofia Georgopoulou, Savia de Souza, Ailsa Bosworth, Lindsay Bearne and Heidi Lempp

      Version of Record online: 18 APR 2016 | DOI: 10.1111/hex.12457

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      We need to talk about purpose: a critical interpretive synthesis of health and social care professionals’ approaches to self-management support for people with long-term conditions

      Heather May Morgan, Vikki A. Entwistle, Alan Cribb, Simon Christmas, John Owens, Zoë C. Skea and Ian S. Watt

      Version of Record online: 14 APR 2016 | DOI: 10.1111/hex.12453

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      End-of-life care decisions for haemodialysis patients – ‘We only tend to have that discussion with them when they start deteriorating’

      Sophia Lazenby, Adrian Edwards, Raymond Samuriwo, Stephen Riley, Mary Ann Murray and Andrew Carson-Stevens

      Version of Record online: 10 MAR 2016 | DOI: 10.1111/hex.12454

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      ‘Who is on your health-care team?’ Asking individuals with heart failure about care team membership and roles

      Kori A. LaDonna, Joanna Bates, Glendon R. Tait, Allan McDougall, Valerie Schulz, Lorelei Lingard and For the Heart Failure/Palliative Care Teamwork Research Group

      Version of Record online: 29 FEB 2016 | DOI: 10.1111/hex.12447

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      Why do pregnant women participate in research? A patient participation investigation using Q-Methodology

      Riwa Meshaka, Stephen Jeffares, Farah Sadrudin, Nicole Huisman and Ponnusamy Saravanan

      Version of Record online: 26 FEB 2016 | DOI: 10.1111/hex.12446

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      Sensitivity to scale of willingness-to-pay within the context of menorrhagia

      Sabina Sanghera, Emma Frew, Janesh Kumar Gupta, Joe Kai and Tracy Elizabeth Roberts

      Version of Record online: 23 FEB 2016 | DOI: 10.1111/hex.12452

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      Cancer screening in Portugal: sex differences in prevalence, awareness of organized programmes and perception of benefits and adverse effects

      Ana Rute Costa, Susana Silva, Pedro Moura-Ferreira, Manuel Villaverde-Cabral, Osvaldo Santos, Isabel do Carmo, Henrique Barros and Nuno Lunet

      Version of Record online: 23 FEB 2016 | DOI: 10.1111/hex.12450

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      The use of decision aids on early detection of prostate cancer: views of men and general practitioners

      Annelies Engelen, Joke Vanderhaegen, Hendrik Van Poppel and Chantal Van Audenhove

      Version of Record online: 18 FEB 2016 | DOI: 10.1111/hex.12451

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