The goal of the ABACUS-HIV Study is to learn about things that make it easier or more difficult for people with HIV to take their cholesterol medication consistently. WHAT WILL YOU BE ASKED TO DO? Be interviewed for 60-75 minutes in clinic or by phone; All your responses will be confidential; Participants will be compensated $50. WHO CAN JOIN? People living with HIV; At least 18 years old; Prescribed a cholesterol medication called a statin; Can speak English; Have agreed to be in the HIV clinic database at UNC. Patients interested in participating should contact the study team at (919) 843-2532.
To enhance community organizations knowledge of the research world
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).
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).
The purpose of this study is to collect feedback and guidance from parents, healthcare providers, and therapists in the development of a pediatric feeding clinic for autistic patients. The goal is to create feeding services that are responsive to the unique needs of this populaiton.
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 compare the effect of bilateral ovarian vein and pelvic vein embolization versus placebo (venography alone) in women with symptoms and signs suggesting venous origin chronic pelvic pain, at least one dilated and incompetent ovarian vein (≥6mm with reflux on any imaging modality) and pelvic varices (≥1 veins, >5 mm diameter) on reducing pain symptoms as measured by difference in visual analog scale (VAS) pain score at 6 months in treatment group vs. control group.
The purpose of this study to understand employee reactions to observations about their work environment, specifically emotions experienced from their coworker's behavior.
Evaluating the processes and impacts of a multi-year research project
This is a Phase 2 Crossover Study of On Demand PrEP Formulations Comparing Rectal and Oral TFV-Based PrEP