748 results on '"Calvert, Melanie"'
Search Results
2. Long COVID research in minority ethnic populations may be lost in translation
3. Author Correction: Concordance of randomised controlled trials for artificial intelligence interventions with the CONSORT-AI reporting guidelines
4. Predictors of quality of life, functional status, depression and fatigue in early arthritis: comparison between clinically suspect arthralgia, unclassified arthritis and rheumatoid arthritis
5. Concordance of randomised controlled trials for artificial intelligence interventions with the CONSORT-AI reporting guidelines
6. Recommendations to address respondent burden associated with patient-reported outcome assessment
7. A framework for implementing patient-reported outcomes in clinical care: the PROTEUS-practice guide
8. A toolkit for capturing a representative and equitable sample in health research
9. The value of standards for health datasets in artificial intelligence-based applications
10. Evaluating patient-reported outcome measures (PROMs) for future clinical trials in adult patients with optic neuritis
11. Considerations for patient and public involvement and engagement in health research
12. The cost of primary care consultations associated with long COVID in non-hospitalised adults: a retrospective cohort study using UK primary care data
13. Development and usability testing of an electronic patient-reported outcome (ePRO) solution for patients with inflammatory diseases in an Advanced Therapy Medicinal Product (ATMP) basket trial
14. “I just wanted to speak to someone- and there was no one…”: using Burden of Treatment Theory to understand the impact of a novel ATMP on early recipients
15. Co-production of a feasibility trial of pacing interventions for Long COVID
16. Core outcome measurement instruments for use in clinical and research settings for adults with post-COVID-19 condition: an international Delphi consensus study
17. The effect of disease modifying therapies on fatigue in multiple sclerosis
18. Perspectives on Patient-Reported Outcome Data After Treatment Discontinuation in Cancer Clinical Trials
19. Patient and public involvement within epidemiological studies of long COVID in the UK
20. Paving the way for patient centricity in real-world evidence (RWE): Qualitative interviews to identify considerations for wider implementation of patient-reported outcomes in RWE generation
21. Identifying patient-valued outcomes for use in early phase trials of ocular surface disease interventions
22. Optimising the selection of outcomes for healthy ageing trials: a mixed methods study
23. Knowledge translation concerns for the CONSORT-PRO extension reporting guidance: a review of reviews
24. Disruptions to the hearing health sector
25. Usability testing of an electronic patient-reported outcome system linked to an electronic chemotherapy prescribing and patient management system for patients with cancer
26. Setting International Standards in Analyzing Patient-Reported Outcomes and Quality of Life Endpoints in Cancer Clinical Trials-Innovative Medicines Initiative (SISAQOL-IMI): stakeholder views, objectives, and procedures
27. Single-arm studies involving patient-reported outcome data in oncology: a literature review on current practice
28. Recommendations on the use of item libraries for patient-reported outcome measurement in oncology trials: findings from an international, multidisciplinary working group
29. Symptoms and risk factors for long COVID in non-hospitalized adults
30. Opportunities and Risks of UK Medical Device Reform
31. Patient reported outcome assessment must be inclusive and equitable
32. The opportunity for greater patient and public involvement and engagement in drug development and regulation
33. Implementation of patient-reported outcome measures in real-world evidence studies: Analysis of ClinicalTrials.gov records (1999–2021)
34. A core outcome set for post-COVID-19 condition in adults for use in clinical practice and research: an international Delphi consensus study
35. Understanding and tracking the impact of long COVID in the United Kingdom
36. Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection
37. Systematic review of guidance for the collection and use of patient-reported outcomes in real-world evidence generation to support regulation, reimbursement and health policy
38. Evaluating patient-reported outcome measures (PROMs) for clinical trials and clinical practice in adult patients with uveitis or scleritis: a systematic review
39. Factors influencing follow-up care post-TIA and minor stroke: a qualitative study using the theoretical domains framework
40. Outcome selection for tissue-agnostic drug trials for immune-mediated inflammatory diseases: a systematic review of core outcome sets and regulatory guidance
41. Anticoagulation in Patients With Device-Detected Atrial Fibrillation With and Without a Prior Stroke or Transient Ischemic Attack: The NOAH-AFNET 6 Trial.
42. Integrating patient and public involvement and engagement in translational medicine.
43. Collaborative care intervention for individuals with severe mental illness: the PARTNERS2 programme including complex intervention development and cluster RCT.
44. The value of patient-reported outcomes in early-phase clinical trials
45. Guidelines for clinical trial protocols for interventions involving artificial intelligence : the SPIRIT-AI Extension
46. Reporting guidelines for clinical trial reports for interventions involving artificial intelligence : the CONSORT-AI Extension
47. What to expect after open heart valve surgery? Changes in health-related quality of life
48. Impact of Using Risk-Based Stratification on Referral of Patients With Chronic Kidney Disease From Primary Care to Specialist Care in the United Kingdom
49. Advancing UK Regulatory Science Strategy in the Context of Global Regulation: a Stakeholder Survey
50. Electronic patient-reported outcomes in chronic kidney disease
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