255 results on '"McMullan, Christel"'
Search Results
2. Implementation of patient and public involvement and engagement (PPIE) for the therapies for long COVID in non-hospitalised individuals (TLC) project
3. Key considerations for digital decentralised clinical trials from a feasibility study assessing pacing interventions for long COVID
4. Opportunities and challenges for patient-reported outcome assessment in multimorbidity research and practice
5. Recommendations to address respondent burden associated with patient-reported outcome assessment
6. Development of a conceptual framework for an electronic patient-reported outcome (ePRO) system measuring symptoms and impacts of CAR T-cell therapies in patients with haematological malignancies
7. Considerations for patient and public involvement and engagement in health research
8. 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
9. Co-production of a feasibility trial of pacing interventions for Long COVID
10. Patient and public involvement within epidemiological studies of long COVID in the UK
11. 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
12. Usability testing of an electronic patient-reported outcome system linked to an electronic chemotherapy prescribing and patient management system for patients with cancer
13. Symptoms and risk factors for long COVID in non-hospitalized adults
14. Patient reported outcome assessment must be inclusive and equitable
15. Development of a quality of life measure for left ventricular assist device recipients using a mixed methods approach.
16. Peer support for carers and patients with inflammatory bowel disease: a systematic review
17. Views and experience of non-hospitalised individuals with Long COVID of using pacing interventions: a mixed methods study
18. Electronic patient-reported outcomes in chronic kidney disease
19. Determining the optimal route of faecal microbiota transplant in patients with ulcerative colitis: the STOP-Colitis pilot RCT.
20. Patient-reported outcomes in integrated health and social care: A scoping review
21. Protocol for a mixed-methods study to develop and feasibility test a digital system for the capture of patient-reported outcomes (PROs) in patients receiving chimeric antigen receptor T-cell (CAR-T) therapies (the PRO-CAR-T study)
22. Patient and Clinician Perspectives on Electronic Patient-Reported Outcome Measures in the Management of Advanced CKD: A Qualitative Study
23. Integrating patient and public involvement and engagement in translational medicine
24. Clinician survey of current global practice for sarcoma surveillance following resection of primary retroperitoneal, abdominal, and pelvic sarcoma
25. The impact of patient-reported outcome data from clinical trials: perspectives from international stakeholders
26. Experiences of patients and their relatives of postoperative radiological surveillance and surveillance intensity following primary resection of a soft tissue sarcoma and its impact on their quality of life: a systematic review protocol
27. TIA and minor stroke: a qualitative study of long-term impact and experiences of follow-up care
28. The impact of patient-reported outcome (PRO) data from clinical trials: a systematic review and critical analysis
29. Digitally enabled decentralised research: opportunities to improve the efficiency of clinical trials and observational studies
30. Non-Pharmacological Therapies for Post-Viral Syndromes, Including Long COVID: A Systematic Review
31. Protocol for a rapid review to inform concept elicitation and measure selection for an electronic patient-reported outcome (ePRO) system for patients with haematological malignancies receiving CAR-T cellular therapies
32. Patient engagement in quality of life research.
33. A realist process evaluation within the Facilitating Implementation of Research Evidence (FIRE) cluster randomised controlled international trial: an exemplar
34. Facilitating Implementation of Research Evidence (FIRE): an international cluster randomised controlled trial to evaluate two models of facilitation informed by the Promoting Action on Research Implementation in Health Services (PARIHS) framework
35. Constructions of Social Exclusion among Young People from Interface Areas of Northern Ireland
36. Feasibility of a new electronic patient-reported outcome (ePRO) system for an advanced therapy clinical trial in immune-mediated inflammatory disease (PROmics): protocol for a qualitative feasibility study
37. Leadership Development in SMEs: An Action Learning Approach
38. Non-pharmacological therapies for post-viral syndromes, including Long COVID: A systematic review
39. Peer Support in Inflammatory Bowel Disease (IBD): A Systematic Review
40. Development and validation of the symptom burden questionnaire for long covid (SBQ-LC): Rasch analysis
41. Therapies for Long COVID in non-hospitalised individuals: from symptoms, patient-reported outcomes and immunology to targeted therapies (The TLC Study)
42. Non-pharmacological therapies for postviral syndromes, including Long COVID: a systematic review and meta-analysis protocol
43. Additional file 1 of Peer support for carers and patients with inflammatory bowel disease: a systematic review
44. Assessment of 115 symptoms for Long COVID (post-COVID-19 condition) and their risk factors in non-hospitalised individuals: a retrospective matched cohort study in UK primary care
45. Development and validation of the Symptom Burden Questionnaire™ for Long Covid: A Rasch analysis
46. ‘I have the worldʼs best job’ – staff experience of the advantages of caring for older people
47. Therapies for Long COVID in non-hospitalised individuals - from symptoms, patient-reported outcomes, and immunology to targeted therapies (The TLC Study): Study protocol
48. Protocol for a scoping review exploring the use of patient-reported outcomes in adult social care
49. Using patient-reported outcome measures during the management of patients with end-stage kidney disease requiring treatment with haemodialysis (PROM-HD): a qualitative study
50. sj-pdf-1-jrs-10.1177_01410768211032850 - Supplemental material for Symptoms, complications and management of long COVID: a review
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