All Stories

  1. Can the Development of Orphan Drugs Include Wider Patient Engagement? A Citizens' Jury to Explore a Promissory Notion
  2. Self-management experiences of people with heart failure with preserved ejection fraction, their caregivers and healthcare professionals: a systematic review and qualitative meta-study
  3. Widening Patient Engagement for Rare Disease Drug Trials: The Perspectives of Patients With Idiopathic Pulmonary Fibrosis on Participating in Clinical Drug Trials and Drug Trial Design
  4. Willingness of people with type 2 diabetes to engage in healthy eating, physical activity and medication taking
  5. How can we improve Comprehensive Geriatric Assessment for older people living with frailty in primary care and community settings? A qualitative study
  6. Understanding joy amongst older people: A scoping review
  7. Liquidity and uncertainty: digital adaptation of a complex intervention for people with severe mental illness during the COVID-19 lockdown
  8. Allied health professionals’ views on important outcomes of children’s elective lower limb orthopaedic surgery: a qualitative interview study to inform a core outcome set
  9. Older Adults’ Perspectives of Independence Through Time: Results of a Longitudinal Interview Study
  10. How do patients and other members of the public engage with the orphan drug development? A narrative qualitative synthesis
  11. Caregiver presence in a home-based cardiac rehabilitation programme improves the health-related quality of life of patients with heart failure
  12. Using simulation and machine learning to maximise the benefit of intravenous thrombolysis in acute stroke in England and Wales: the SAMueL modelling and qualitative study
  13. Use of Clinical Pathway Simulation and Machine Learning to Identify Key Levers for Maximizing the Benefit of Intravenous Thrombolysis in Acute Stroke
  14. Evaluation of a primary care-based collaborative care model (PARTNERS2) for people with diagnoses of schizophrenia, bipolar, or other psychoses: study protocol for a cluster randomised controlled trial
  15. Process evaluation of a randomised pilot trial of home-based rehabilitation compared to usual care in patients with heart failure with preserved ejection fraction and their caregiver’s
  16. What is Morita Therapy? The Nature, Origins, and Cross-Cultural Application of a Unique Japanese Psychotherapy
  17. The value of social practice theory for implementation science: learning from a theory-based mixed methods process evaluation of a randomised controlled trial
  18. Learning from a Feasibility Trial of a Simple Intervention: Is Research a Barrier to Service Delivery, or is Service Delivery a Barrier to Research?
  19. Patients' and nurses' experiences of fundamental nursing care: A systematic review and qualitative synthesis
  20. Integrating quantitative and qualitative data and findings when undertaking randomised controlled trials
  21. Home-based rehabilitation for heart failure with reduced ejection fraction: mixed methods process evaluation of the REACH-HF multicentre randomised controlled trial
  22. Does a simple web-based intervention facilitate the articulation of patients’ unvoiced agenda for a consultation with their diabetologists? A qualitative study
  23. Morita Therapy for depression (Morita Trial): an embedded qualitative study of acceptability
  24. The effects and costs of home-based rehabilitation for heart failure with reduced ejection fraction: The REACH-HF multicentre randomized controlled trial
  25. Patient involvement in qualitative data analysis in a trial of a patient-centred intervention: Reconciling lay knowledge and scientific method
  26. Morita Therapy for depression (Morita Trial): a pilot randomised controlled trial
  27. Amalgamation of Marginal Gains (AMG) as a potential system to deliver high-quality fundamental nursing care: A qualitative analysis of interviews from high-performance AMG sports and healthcare practitioners
  28. Fundamental nursing care: A systematic review of the evidence on the effect of nursing care interventions for nutrition, elimination, mobility and hygiene
  29. Optimising the acceptability and feasibility of novel complex interventions: an iterative, person-based approach to developing the UK Morita therapy outpatient protocol
  30. Behind the smile: qualitative study of caregivers’ anguish and management responses while caring for someone living with heart failure
  31. N of 1 trials and the optimal individualisation of drug treatments: a systematic review protocol
  32. A preconsultation web-based tool to generate an agenda for discussion in diabetes outpatient clinics to improve patient outcomes (DIAT): a feasibility study
  33. How people with progressive multiple sclerosis give meaning to their experiences.
  34. Optimising self-care support for people with heart failure and their caregivers: development of the Rehabilitation Enablement in Chronic Heart Failure (REACH-HF) intervention using intervention mapping
  35. Morita therapy for depression and anxiety (Morita Trial): study protocol for a pilot randomised controlled trial
  36. Meta-study as Diagnostic
  37. Context and complexity: the meaning of self-management for older adults with heart disease
  38. Person-centred care in dentistry - the patients' perspective
  39. Needs of caregivers in heart failure management: A qualitative study
  40. Dental patients: Delivering PCC
  41. A qualitative synthesis of diabetes self-management strategies for long term medical outcomes and quality of life in the UK
  42. Patient-centred care in general dental practice - a systematic review of the literature
  43. Individualisation of drug treatments for patients with long-term conditions: a review of concepts
  44. Processes of Change in an Asthma Self-Care Intervention
  45. Patient-centred care in general dental practice: sound sense or soundbite?
  46. A pilot randomised controlled trial of a preconsultation web-based intervention to improve the care quality and clinical outcomes of diabetes outpatients (DIAT)
  47. Using meta-ethnography to understand the emotional impact of caring for people with increasing cognitive impairment
  48. Doctors’ understanding of individualisation of drug treatments: a qualitative interview study
  49. Women’s views on the use of decision aids for decision making about the method of delivery following a previous caesarean section: qualitative interview study
  50. Review: Family communication about cystic fibrosis from the mother's perspective: an exploratory study
  51. The loss of possibility: scientisation of death and the special case of early miscarriage
  52. Exploring the Dirty Side of Women's Health
  53. Utopian Theory and the Discourse of Natural Birth