To assess how the Medical Staff of UNC view interventions to prevent COVID acquisition

This study explores the physical features and everyday use of shared water, sanitation, and energy services in informal settlement, Nairobi. It looks at what these shared facilities are like, how people use and take care of them, and how they deal with problems such as flooding or damage. By learning from people's experiences, the study hopes to find better ways to improve these shared facilities in crowded urban areas.

The purpose of this study is to determine the association of one or more fall-risk assessments tools and joint ROM data to fall, near fall, injurious fall, and fear of falling in the hemophilia population

This study explores how nursing faculty in Saudi Arabia perceive the integration of genetics and genomics into undergraduate curricula. The goal is to understand faculty preparedness, institutional support, and barriers to implementation.

This registry will collect data on the strategies used to achieve a diagnosis of Idiopathic Pulmonary Fibrosis (IPF) and Chronic Fibrosing Interstitial Lung Disease with Progressive Phenotype (ILD) and the treatment and management efforts applied throughout study follow-up, clinical outcome events and patient reported outcome data. Blood samples will be collected periodically throughout the study for use in future research efforts. For participants with non-IPF, chronic fibrosing ILD with progressive phenotype, HRCT images will be collected throughout the study for use in future research efforts.

We are studying the effects of early antibiotic use on the bacteria in the gut and how this effects the lung mucus

The purpose of this research study is to understand better how to involve children and parents during medical visits.

To support Indigenous peoples who wish to better govern data produced about them by developing an Amazonian-centered approach to digital governance that can support Indigenous conceptions of the world and help reduce the risks of imposing non-local theories of value that serve interests elsewhere.

Now called the Pediatric Heart Transplant Society (PHTS), the Pediatric Heart Transplant Study Registry was established in 1993 by a group of physicians who wanted to improve the lives of children who needed a heart transplant. The primary purposes of the organization was to establish and maintain a prospective, event driven database for heart transplantation, to encourage and stimulate basic and clinical research in the field of pediatric heart transplantation, and to promote new therapeutic strategies. The ultimate goal was to improve the lives of pediatric heart transplant recipients.

To examine the relationship of queer culture, body neutrality/positivity, and exercise-related stigma and anxiety in a specialized yoga setting.