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3. What to Measure in Aneurysmal Subarachnoid Haemorrhage Research—An International Delphi Survey

4. Behavior Change Techniques Included in Reports of Social Media Interventions for Promoting Health Behaviors in Adults: Content Analysis Within a Systematic Review

5. Pragmatic Strategy Empowering Paramedics to Assess Low-Risk Trauma Patients With the Canadian C-Spine Rule and Selectively Transport Them Without Immobilization: Protocol for a Stepped-Wedge Cluster Randomized Trial

6. Protocol for the development of guidance for collaborator and partner engagement in health care evidence syntheses

7. “I’d like more options!”: Interviews to explore young people and family decision-making needs for pain management in juvenile idiopathic arthritis

8. Improving social justice in observational studies: protocol for the development of a global and Indigenous STROBE-equity reporting guideline

9. Developing an Outcome Measures in Rheumatology (OMERACT) Core set of Outcome Measures for FOot and ankle disorders in RheumaTic and musculoskeletal diseases (COMFORT): core domain set study protocol

10. Prioritising Cochrane reviews to be updated with health equity focus

11. Key issues for stakeholder engagement in the development of health and healthcare guidelines

17. Defining domains: developing consensus-based definitions for foundational domains in OMERACT core outcome sets

19. Establishing a Core Outcome Measure for Peritoneal Dialysis-related Peritonitis: A Standardized Outcomes in Nephrology—Peritoneal Dialysis Consensus Workshop Report

20. Presenting Evidence to Patients Online: What Do Web Users Think of Consumer Summaries of Cochrane Musculoskeletal Reviews?

21. Motivations for investigating health inequities in observational epidemiology: a content analysis of 320 studies

22. Methods proposed for monitoring the implementation of evidence-based research: a cross-sectional study

23. Evolving and evaluating the OMERACT fellows program: insights and implications from OMERACT 2023 fellows

24. The Sjögren's Working Group: The 2023 OMERACT meeting and provisional domain generation

25. Consensus on the definitions and descriptions of the domains of the OMERACT Core Outcome Set for shared decision making interventions in rheumatology trials

26. Generating a list of potentially important contextual factors covering randomized trials, cohorts, and measurement property studies: An OMERACT initiative

27. OMERACT Core outcome measurement set for shared decision making in rheumatic and musculoskeletal conditions: a scoping review to identify candidate instruments

28. Patient outcomes in longitudinal observational studies (POLOS) of rheumatoid arthritis: Determining the OMERACT core domain set

30. Developing consensus on core outcome sets of domains for acute, the transition from acute to chronic, recurrent/episodic, and chronic pain: results of the INTEGRATE-pain Delphi process

31. Stakeholder endorsement advancing the implementation of a patient-reported domain for harms in rheumatology clinical trials: Outcome of the OMERACT Safety Working Group

33. Factors to Consider During Identification and Invitation of Individuals in a Multi-stakeholder Research Partnership

35. Equity issues rarely addressed in the development of COVID-19 formal recommendations and good practice statements: a cross-sectional study

36. Improving the quality of toxicology and environmental health systematic reviews: What journal editors can do.

37. Developing a core outcome set for foot and ankle disorders in rheumatic and musculoskeletal diseases: A scoping review and report from the OMERACT 2022 foot and ankle special interest group session

38. A scoping review establishes need for consensus guidance on reporting health equity in observational studies

39. Outcome reporting in randomized trials in gout: A systematic scoping review from the OMERACT gout working group assessing the uptake of the core outcome set

41. Geographical and Gender Diversity in Cochrane and non-Cochrane Reviews Authorship: A Meta-Research Study

42. Reporting of equity in observational epidemiology: A methodological review

43. Considering health equity when moving from evidence-based guideline recommendations to implementation : a case study from an upper-middle income country on the GRADE approach

47. Implementing core outcomes in kidney disease: report of the Standardized Outcomes in Nephrology (SONG) implementation workshop

48. A multistakeholder development process to prioritize and translate COVID-19 health recommendations for patients, caregivers and the public. A case study of the COVID-19 recommendation map

49. An evaluation of the COVID-19 recommendation map identified diverging clinical and public health guidance

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