A primary objective is to collect data on key clinical outcome endpoints, including changes in percent predicted forced expiratory volume in one second (ppFEV1) that are often used as endpoints in therapeutic trials to establish a repository of control data (e.g., in the absence of investigational drug use) in pwCF who are ineligible and/or not taking CFTR modulators. These data may be used in research or investigative efforts (e.g., for comparison with people exposed to experimental or new therapies in CF).

The purpose of this research is to analyze and confirm the parallel of stigma and masculinity in mental health and help-seeking intentions among college football players and Marines.

To implement and analyze validity evidence of a standardized readout assessment form for each of the subspecialties of radiology (nuclear medicine, pediatrics, abdomen, chest, musculoskeletal, breast, interventional radiology, neuroradiology, and emergency medicine).

We Yone Foundation and Georgina (Gina) Adatsi are carrying out this qualitative study on measuring the level of reproductive health knowledge that teenage boys and girls already have here in Freetown, Sierra Leone. Your child's participation in this study will help improve our understanding of gaps within reproductive health, how reproductive health is understood, understanding female/male anatomy, and the importance of family planning methods. It will also inform us on how gaps in knowledge lead to higher rates of teenage pregnancy. Researchers will use the results of this study to inform policy makers and actors working in the area of family planning and to reduce teenage pregnancy. We want to be sure that you understand the purpose of this research and your responsibilities in it before you decide if you want your child to participate in the study. Please ask us to explain any words or information you do not

This study aims to develop a blood test to track, locate, and diagnose aortic aneurysm disease.

To test if study drug can help improve well being of patients with heart failure

The purpose of the registry is to better characterize physical characteristics of patients with peripheral neuropathies and generate a group of well-studied patients.

To enhance community organizations knowledge of the research world

This study will use group model building methodologies to understand the dynamics preventing punitive policy change (de-implementation) for pregnant persons who use substances. We will be recruiting those involved in this process (e.g., policymakers, agency staff members, clinicians, and social workers, etc.).

The overarching aim of the broader research project is to evaluate health insurance enrollment assister (aka Navigator) programs in North Carolina and document the additional support Navigators provide clients beyond assistance with health insurance. This portion of the study involves interviewing health insurance navigators about their experiences, particularlly regarding: 1. Types of support (health insurance and non-health insurance-related) 2. Challenges and best practices of supporting members 3. Strategies for reaching marginalized communities