1,025 results on '"Hopewell, Sally"'
Search Results
2. Methods used to develop the SPIRIT 2024 and CONSORT 2024 Statements
3. Patient-relevant outcomes following elective, aseptic revision knee arthroplasty: a systematic review
4. Development of consensus-driven SPIRIT and CONSORT extensions for early phase dose-finding trials: the DEFINE study
5. Recommendations for progression criteria during external randomised pilot trial design, conduct, analysis and reporting
6. Determining external randomised pilot trial feasibility in preparation for a definitive trial: a web-based survey of corresponding authors of external pilot trial publications
7. Pilot and feasibility studies: extending the conceptual framework
8. Tailored exercise management (TEMPO) versus usual care for people aged 80 years or older with hip/knee osteoarthritis: study protocol for a feasibility randomised controlled trial
9. Patient-Relevant Outcomes Following First Revision Total Knee Arthroplasty, by Diagnosis: An Analysis of Implant Survivorship, Mortality, Serious Medical Complications, and Patient-Reported Outcome Measures Utilizing the National Joint Registry Data Set
10. A scoping review identifies multiple comments suggesting modifications to SPIRIT 2013 and CONSORT 2010
11. An update to SPIRIT and CONSORT reporting guidelines to enhance transparency in randomized trials
12. CONSORT and Its Extensions for Reporting Clinical Trials
13. Development of a topic‐specific bibliographic database supporting the updates of SPIRIT 2013 and CONSORT 2010
14. Anti-TNF (adalimumab) injection for the treatment of pain-predominant early-stage frozen shoulder: the Anti-Freaze-Feasibility randomised controlled trial
15. A meta-research study of randomized controlled trials found infrequent and delayed availability of protocols
16. How are progression decisions made following external randomised pilot trials? A qualitative interview study and framework analysis
17. Inclusion of progression criteria in external randomised pilot trials: a cross-sectional study of funding applications submitted to the NIHR Research for Patient Benefit Programme
18. A longitudinal assessment of trial protocols approved by research ethics committees: The Adherance to SPIrit REcommendations in the UK (ASPIRE-UK) study
19. Evaluation of cultural competency in a South African cluster randomised controlled trial: lessons learned for trial reporting standards
20. Pharmacological interventions for early-stage frozen shoulder: a systematic review and network meta-analysis
21. Reporting quality of trial protocols improved for non-regulated interventions but not regulated interventions: A repeated cross-sectional study
22. Progressive exercise compared with best practice advice, with or without corticosteroid injection, for the treatment of patients with rotator cuff disorders (GRASP): a multicentre, pragmatic, 2 × 2 factorial, randomised controlled trial
23. A meta-research study revealed several challenges in obtaining placebos for investigator-initiated drug trials
24. Reports of randomised control trials should begin and conclude with up-to-date systematic reviews of other relevant trials: a 25-year audit of the quality of trial reports.
25. Development and implementation of the physiotherapy-led exercise interventions for the treatment of rotator cuff disorders for the ‘Getting it Right: Addressing Shoulder Pain’ (GRASP) trial
26. Reporting of Factorial Randomized Trials
27. Consensus Statement for Protocols of Factorial Randomized Trials
28. Hospital-based caregiver intervention for people following hip fracture surgery (HIP HELPER): multicentre randomised controlled feasibility trial with embedded qualitative study in England
29. Perspectives of informal caregivers who support people following hip fracture surgery: a qualitative study embedded within the HIP HELPER feasibility trial
30. RoB 2 : a revised tool for assessing risk of bias in randomised trials
31. Randomised study within a trial (SWAT) to evaluate personalised versus standard text message prompts for increasing trial participant response to postal questionnaires (PROMPTS)
32. Findings from the patch augmented rotator cuff surgery (PARCS) feasibility study
33. Transparency of informed consent in pilot and feasibility studies is inadequate: a single-center quality assurance study
34. An overview of systematic reviews found suboptimal reporting and methodological limitations of mediation studies investigating causal mechanisms
35. The need for reporting guidelines for early phase dose-finding trials: Dose-Finding CONSORT Extension
36. Enhancing reporting quality and impact of early phase dose-finding clinical trials: CONSORT Dose-finding Extension (CONSORT-DEFINE) guidance
37. Strengthening programme for ambulant adolescents with cerebral palsy
38. CONSORT and Its Extensions for Reporting Clinical Trials
39. The Effect of Therapeutic Exercise Interventions on Physical and Psychosocial Outcomes in Adults Aged 80 Years and Older: A Systematic Review and Meta-Analysis.
40. Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis
41. Reporting Quality of Journal Abstracts for Surgical Randomized Controlled Trials Before and After the Implementation of the CONSORT Extension for Abstracts
42. Overinterpretation and misreporting of prognostic factor studies in oncology: a systematic review
43. Reminding Peer Reviewers of Reporting Guideline Items to Improve Completeness in Published Articles
44. Restrictive versus liberal blood transfusion for gastrointestinal bleeding: a systematic review and meta-analysis of randomised controlled trials
45. Impact of grey literature on systematic reviews of randomized trials
46. Rationale and design of repeated cross-sectional studies to evaluate the reporting quality of trial protocols: the Adherence to SPIrit REcommendations (ASPIRE) study and associated projects
47. Progressive exercise compared with best practice advice, with or without corticosteroid injection, for the treatment of rotator cuff disorders: statistical analysis plan for the Getting it Right: Addressing Shoulder Pain (GRASP) 2 × 2 factorial multicentre randomised controlled trial
48. Prediction of RECRUITment In randomized clinical Trials (RECRUIT-IT)—rationale and design for an international collaborative study
49. Development of A Guideline for Reporting Mediation Analyses (AGReMA)
50. Accuracy in detecting inadequate research reporting by early career peer reviewers using an online CONSORT-based peer-review tool (COBPeer) versus the usual peer-review process: a cross-sectional diagnostic study
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