This study seeks to explore the specific needs of alternatively licensed teachers in their first year of teaching.

We are recruiting 216 people at events in the community to look at different types of educational materials about genomics. We will survey them before and after to see if and how their knowledge and willingness to participate in research was affected. Then, we will ask 30 of those people to participate in a 45-60 minute interview over Zoom. This will help us to gather more information about their preferences and attitudes toward genomic research. We will be recruiting from a diverse group of people and offering materials in both English and Spanish. The purpose of this is to improve health literacy and willingness of participate in genomic research in order to improve health equity.

A survey about long-acting injectable medications will be sent to pharmacists in North Carolina who work in the community or outpatient settings.

This research will examine the variable ways that people have used and interpreted collections related to the Greensboro Massacre in Wilson Library, and how they conceptualize their research in relation to memory, history, and justice. This project will involve semi-structured interviews with five to eight researchers, working to understand how the interviewees interpret and disseminate their findings from the archive. Afterwards, I will compare interview responses, in order to trace common and divergent themes. I will interview both academic researchers, as well as community historians and activists.

The purpose of this project is to complete the complete CVI Range assessment (Roman-Lantzy, 2018) and the Communication Matrix (Rowland, 2011) on a group of children with Angelman syndrome. The results will increase understandings of Cortical Visual Impairment (CVI) and its relationship to symbolic communication in this population.

The research study seeks to improve the effectiveness of warnings for little cigars and cigarillos (LCCs) among youth who currently use, have ever used, or are susceptible to using LCCs

No guidelines or interventions for patients and their family caregivers exist to support patient adherence to a new medication (venetoclax) and their quality of life. Our research team seeks to understand the real experience and care needs of patients and their family caregivers with the new AML treatment. With the information we learn from this study, we will be able to develop an effective support program for patients with AML and their family caregivers to manage their symptoms at home and improve their quality of life.

Interviews are being conducted to establish a set of criteria for gauging the success or failure of corporate rebranding campaigns.

Screening tool to collect broader demographic and clinical data. Enhance understanding of site specific and trial specific accrual barriers.

In this study, we aim to assess patient, their partner, and provider understanding of a diagnosis of polycystic ovary syndrome (PCOS). An electronic survey investigating respondent's knowledge of the key clinical features of PCOS will be distributed to patients with PCOS and their partners, as well as to attending and resident physicians from various specialties and medical students. We believe that this study will highlight areas of clinical confusion to patients and areas where providers can improve upon counseling and patient education regarding features of the disease. We also believe that this study may highlight disparities in knowledge and understanding of key clinical features of PCOS among various providers, potentially highlighting an opportunity for improved training and education among physicians at various levels of training.