A5043347658- Vaccine Coverage and Hesitancy
- SARS-CoV-2 and COVID-19 Research
- Multiple Sclerosis Research Studies
- Bacillus and Francisella bacterial research
- Systemic Lupus Erythematosus Research
- Rheumatoid Arthritis Research and Therapies
- Acute Lymphoblastic Leukemia research
- Health Literacy and Information Accessibility
- Ethics in medical practice
- Polyomavirus and related diseases
- Health Systems, Economic Evaluations, Quality of Life
- Mental Health and Patient Involvement
- Peripheral Neuropathies and Disorders
- Healthcare Policy and Management
Mammoth Hospital
2021
International AIDS Vaccine Initiative
2021
National Multiple Sclerosis Society
2021
Massachusetts General Hospital
2021
Accelerated Cure Project for Multiple Sclerosis
2021
Quest Diagnostics (United States)
2021
Yale University
2021
University of Dayton
2013-2015
Research Network (United States)
2015
Pragmatic research that compares interventions to improve the organization and delivery of health care may overlap, in both goals methods, with quality improvement activities. When activities have attributes improvement, confusion often arises about what ethical oversight is, or should be, required. For routine which is modified minor ways create only minimal risks, by local clinical administrative leaders utilizing institutional policies be sufficient. However, additional consideration...
There are limited data on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine reactogenicity in persons with multiple sclerosis (PwMS) and how is affected by disease-modifying therapies (DMTs). The objective of this retrospective cross-sectional study was to generate real-world sclerosis-specific safety information, particularly the context specific DMTs, provide information mitigate concerns hesitant PwMS.Between 3/2021 6/2021, participants iConquerMS, an online...
Patient-Powered Research Networks (PPRNs) are US-based registry infrastructures co-created by advocacy groups, patient research partners, academic investigators, and other healthcare stakeholders. collect information directly from patients to conduct disseminate the results of patient-centered/powered that helps make more informed decisions about their healthcare. gather utilize real-world data patient-reported outcomes comparative effectiveness, safety, research, leverage Internet...