245 results on '"Snowdon, Claire"'
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2. Operational complexity versus design efficiency: challenges of implementing a phase IIa multiple parallel cohort targeted treatment platform trial in advanced breast cancer
3. Practical guidance for planning resources required to support publicly-funded adaptive clinical trials
4. The SHOW RESPECT adaptable framework of considerations for planning how to share trial results with participants, based on qualitative findings from trial participants and site staff.
5. Circulating tumour DNA analysis to direct therapy in advanced breast cancer (plasmaMATCH): a multicentre, multicohort, phase 2a, platform trial
6. How surgical Trainee Research Collaboratives achieve success: a mixed methods study to develop trainee engagement strategies
7. Costs and staffing resource requirements for adaptive clinical trials: quantitative and qualitative results from the Costing Adaptive Trials project
8. Cediranib in patients with alveolar soft-part sarcoma (CASPS): a double-blind, placebo-controlled, randomised, phase 2 trial
9. Site staff perspectives on communicating trial results to participants: Cost and feasibility results from the Show RESPECT cluster randomised, factorial, mixed-methods trial
10. Testing approaches to sharing trial results with participants: The Show RESPECT cluster randomised, factorial, mixed methods trial
11. Adapting Patient and Public Involvement processes in response to the Covid‐19 pandemic
12. Collaboration, participation and non-participation : decisions about involvement in randomised controlled trials for clinicians and parents in two neonatal trials
13. Clinical effectiveness and cost-effectiveness of emergency surgery for adult emergency hospital admissions with common acute gastrointestinal conditions: the ESORT study
14. Patient advocate involvement in the design and conduct of breast cancer clinical trials requiring the collection of multiple biopsies
15. Additional file 1 of Practical guidance for planning resources required to support publicly-funded adaptive clinical trials
16. Additional file 1 of Practical guidance for running late-phase platform protocols for clinical trials: lessons from experienced UK clinical trials units
17. Information-hungry and disempowered: A qualitative study of women and their partners' experiences of severe postpartum haemorrhage
18. Views of emergency research (VERA): A qualitative study of women and their partners' views of recruitment to trials in severe postpartum haemorrhage
19. Practical Guidance for Running Late-Phase Platform Protocols for Clinical Trials: Lessons From Experienced UK Clinical Trials Units
20. Abstract OT2-05-01: The HER2-RADiCAL study (Response ADaptive CAre pLan) - Tailoring treatment for HER2 positive early breast cancer
21. Abstract GS3-06: Primary results of the cTRAK TN trial: A clinical trial utilising ctDNA mutation tracking to detect minimal residual disease and trigger intervention in patients with moderate and high risk early stage triple negative breast cancer
22. Using a theory-informed approach to explore patient and staff perspectives on factors that influence clinical trial recruitment for patients with cirrhosis and small oesophageal varices
23. Fifteen-minute consultation: an evidence-based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials
24. Trial Experience And Problems Of Parental Recollection Of Consent
25. Benefits and challenges of electronic data capture (EDC) systems versus paper case report forms
26. “You have to keep your nerve on a DMC.” Challenges for data monitoring committees in neonatal intensive care trials: qualitative accounts from the bracelet study
27. Design considerations when transitioning from paper case report forms (CRFS) to electronic data capture (EDC)
28. Implementing electronic data capture (EDC) training for site staff
29. Additional file 1 of Costs and staffing resource requirements for adaptive clinical trials: quantitative and qualitative results from the Costing Adaptive Trials project
30. Reactions of Participants to the Results of a Randomised Controlled Trial: Exploratory Study
31. Informed Consent
32. A Critical Discourse Analysis of Representations of Travellers in Public Policies in Ireland
33. Skeletal effects of exemestane on bone-mineral density, bone biomarkers, and fracture incidence in postmenopausal women with early breast cancer participating in the Intergroup Exemestane Study (IES): a randomised controlled study
34. 'It was a snap decision': Parental and professional perspectives on the speed of decisions about participation in perinatal randomised controlled trials
35. Patient and public involvement prior to trial initiation: lessons learnt for rapid partnership in the COVID-19 era.
36. Life After COVID-19 for Cancer Clinical Trials
37. The decision to decline to enrol in a clinical trial: a blind spot in the literature on decision-making for research participation
38. Directing Therapy with Circulating Tumor DNA Analysis in Advanced Breast Cancer: The PlasmaMATCH Trial
39. Development of a standardised set of metrics for monitoring site performance in multicentre randomised trials: a Delphi study
40. Quality of Life in the Intergroup Exemestane Study: A Randomized Trial of Exemestane Versus Continued Tamoxifen After 2 to 3 Years of Tamoxifen in Postmenopausal Women With Primary Breast Cancer
41. Making sense of randomization: responses of parents of critically ill babies to random allocation of treatment in a clinical trial
42. A Randomized Trial of Exemestane after Two to Three Years of Tamoxifen Therapy in Postmenopausal Women with Primary Breast Cancer
43. Randomized Phase II Study Evaluating Palbociclib in Addition to Letrozole as Neoadjuvant Therapy in Estrogen Receptor–Positive Early Breast Cancer: PALLET Trial
44. The BRACELET Study: surveys of mortality in UK neonatal and paediatric intensive care trials
45. Control of hyperglycaemia in paediatric intensive care (CHiP): study protocol
46. Informed consent: Subjects may not understand concept of clinical trials
47. Patient and public involvement prior to trial initiation: lessons learnt for rapid partnership in the COVID-19 era.
48. Marketing and clinical trials: a case study
49. 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
50. Clinical trials and neonatal intensive care
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