145 results on '"Gavigan, Kelly"'
Search Results
2. COVID‐19 Vaccine Uptake, Hesitancy, and Flare in a Large Rheumatology Practice Network
3. Correction: Experiences and Treatment Preferences in Patients With Psoriatic Arthritis: A Cross-Sectional Study in the ArthritisPower Registry
4. Which education topics and smartphone app functions are prioritized by U.S. rheumatology patients? A mixed-methods study
5. Cannabis for Rheumatic Disease Pain: a Review of Current Literature
6. Experiences and Treatment Preferences in Patients With Psoriatic Arthritis: A Cross-Sectional Study in the ArthritisPower Registry
7. Employment, Work Productivity, and Biologic Treatments in Self-Reported Axial Spondyloarthritis: a Cross-Sectional Study in a Female Predominant Population from the ArthritisPower Registry
8. Patient Perspectives on Biologics for Axial Spondyloarthritis in a Cross-sectional Study in a Predominantly Female Population: Treatment Satisfaction, Wear-off Between Doses, and Use of Supplemental Medication
9. Accessibility of adult immunizations in pharmacies compared to physician offices in low-income communities
10. Patient-Reported Nausea and Fatigue Related to Methotrexate: A Prospective, Self-Controlled Study in the ArthritisPower® Registry
11. Protocol for the pilot randomized trial of the CArdiovascular Risk assEssment for Rheumatoid Arthritis (CARE RA) intervention: a peer coach behavioral intervention
12. Patient Perceptions and Preferences Regarding Telemedicine for Autoimmune Rheumatic Diseases Care During the COVID‐19 Pandemic
13. Home‐Based Telemedicine in Rheumatology—A Scoping Review.
14. Medication Interruptions and Subsequent Disease Flares During the COVID‐19 Pandemic: A Longitudinal Online Study of Patients With Rheumatic Disease
15. Participant Engagement and Adherence to Providing Smartwatch and Patient-Reported Outcome Data: Digital Tracking of Rheumatoid Arthritis Longitudinally (DIGITAL) Real-World Study
16. Which patient-reported outcomes do rheumatology patients find important to track digitally? A real-world longitudinal study in ArthritisPower
17. COVID‐19 Vaccine Uptake, Hesitancy, and Flare in a Large Rheumatology Practice Network
18. Understanding Heterogeneity in Patients’ Conceptualisation of Treatment for Rheumatoid Arthritis: A Cluster Analysis
19. Patient Perceptions of Rheumatoid Arthritis Blood Work: A Cross‐Sectional Survey in the ArthritisPower Registry
20. Patient Perceptions of Unmet Medical Need in Rheumatoid Arthritis: A Cross-Sectional Survey in the USA
21. Real-World Patient Experience on the Path to Diagnosis of Ankylosing Spondylitis
22. Balancing COVID ‐19 Risk With Physical and Mental Wellness: Perspectives of Patients With Autoimmune Rheumatic Diseases Throughout the Pandemic
23. Engaging Multistakeholder Perspectives to Identify Patient‐Centered Research Priorities Regarding Vaccine Uptake Among Adults With Autoimmune Conditions
24. Barriers to treatment optimization and achievement of patients’ goals: perspectives from people living with rheumatoid arthritis enrolled in the ArthritisPower registry
25. Wearable Activity Tracker Study Exploring Rheumatoid Arthritis Patients’ Disease Activity Using Patient-Reported Outcome Measures, Clinical Measures, and Biometric Sensor Data (the Wear Study)
26. Participant engagement and adherence in a real-world study to capture smartwatch and patient-reported outcome data in rheumatoid arthritis. (Preprint)
27. Additional file 1 of Protocol for the pilot randomized trial of the CArdiovascular Risk assEssment for Rheumatoid Arthritis (CARE RA) intervention: a peer coach behavioral intervention
28. Additional file 2 of Protocol for the pilot randomized trial of the CArdiovascular Risk assEssment for Rheumatoid Arthritis (CARE RA) intervention: a peer coach behavioral intervention
29. Additional file 3 of Protocol for the pilot randomized trial of the CArdiovascular Risk assEssment for Rheumatoid Arthritis (CARE RA) intervention: a peer coach behavioral intervention
30. Additional file 4 of Protocol for the pilot randomized trial of the CArdiovascular Risk assEssment for Rheumatoid Arthritis (CARE RA) intervention: a peer coach behavioral intervention
31. Patient Perspectives on Biologics for Axial Spondyloarthritis in a Cross-sectional Study in a Predominantly Female Population: Treatment Satisfaction, Wear-off Between Doses, and Use of Supplemental Medication
32. Patient-Reported Nausea and Fatigue Related to Methotrexate: A Prospective, Self-Controlled Study in the ArthritisPower® Registry
33. Treatment Satisfaction and Decision‐making from the Patient Perspective in Axial Spondyloarthritis: Real‐World Data from a Descriptive Cross‐sectional Survey Study from the ArthritisPower Registry
34. Additional file 1 of Which patient-reported outcomes do rheumatology patients find important to track digitally? A real-world longitudinal study in ArthritisPower
35. Social Distancing, Health Care Disruptions, Telemedicine Use, and Treatment Interruption During the COVID‐19 Pandemic in Patients With or Without Autoimmune Rheumatic Disease
36. MOESM4 of Patient perspectives on the pathway to psoriatic arthritis diagnosis: results from a web-based survey of patients in the United States
37. MOESM1 of Barriers to treatment optimization and achievement of patients’ goals: perspectives from people living with rheumatoid arthritis enrolled in the ArthritisPower registry
38. Concerns, Healthcare Use, and Treatment Interruptions in Patients With Common Autoimmune Rheumatic Diseases During the COVID-19 Pandemic
39. Patient-Reported Nausea and Fatigue Related to Methotrexate: A Prospective, Self-Controlled Study in the ArthritisPower® Registry.
40. Treatment Satisfaction and Decision‐making from the Patient Perspective in Axial Spondyloarthritis: Real‐World Data from a Descriptive Cross‐sectional Survey Study from the ArthritisPower Registry.
41. EP30 Understanding which patient-reported outcomes are important to rheumatology patients: findings from ArthritisPower
42. Patient perspectives on the pathway to psoriatic arthritis diagnosis: results from a web-based survey of patients in the United States
43. Prevention literacy: community-based advocacy for access and ownership of the HIV prevention toolkit
44. Concerns, Healthcare Use, and Treatment Interruptions in Patients With Common Autoimmune Rheumatic Diseases During the COVID-19 Pandemic.
45. Digital Tracking of Rheumatoid Arthritis Longitudinally (DIGITAL) Using Biosensor and Patient-Reported Outcome Data: Protocol for a Real-World Study
46. THU0644 PATIENTS’ PERCEPTION AND USE OF MEDICAL MARIJUANA
47. AB1222 PATIENT PREFERENCES FOR THE USE OF DIGITAL TOOLS AND SOCIAL MEDIA IN DIET AND EXERCISE INTERVENTIONS
48. Digital Tracking of Rheumatoid Arthritis Longitudinally (DIGITAL) Using Biosensor and Patient-Reported Outcome Data: Protocol for a Real-World Study (Preprint)
49. Digital Interventions to Build a Patient Registry for Rheumatology Research
50. Effects of the COVID‐19 Pandemic on Patients Living With Vasculitis.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.