In Aim 1, we will use existing research and expert review to develop new text and pictorial LCC warnings and test the new warnings using online experiments to identify warnings that adult LCC users perceive as most effective. The proposed study will fill critical gaps regarding which characteristics make LCC warning labels most effective and provide needed evidence on how LCC warnings influence LCC behavioral intentions. Our overarching goal is to develop effective LCC warnings that reduce cancer and other health risks.

he purpose of Parents and Infants Inter(X)action Intervention (PIXI) is to study ways of supporting the early development of infants diagnosed with rare neurogenetic disorders in their first year of life. PIXI is funded by the John Merck Fund and is led by RTI International (RTI) in collaboration with researchers at the University of North Carolina Chapel Hill. The team includes neurodevelopmental psychologists, early interventionists, and experts in neurogenetic conditions (e.g., fragile X syndrome, Angelman syndrome), autism spectrum disorder, and early childhood development. The goal of PIXI is to provide developmental and behavioral support for infants with rare neurogenetic disorders through a two-phase targeted parent-mediated intervention program.

This research study aims to identify the national need of family medicine residency educators regarding point-of-care ultrasound (POCUS) education and resources. The study will collect data on the state of POCUS education and resources at medical universities across the country through an optional survey sent to faculty who are members of the Society of Teachers of Family Medicine. The questions in the survey focus on the respondee's level of POCUS training, use of POCUS in their day-to-day practice, and desire for different forms of POCUS content to integrate into their residency programs. The data will be collected and evaluated using Qualtrics.

The purpose of this study is to measure different immmune markers in the nasal lining in healthy patients taking Flonase, an over-the-counter steroid nasal spray.

Some female cancers may be genetic, meaning they are passed down from a parent through DNA (our genetic code or roadmap). In people with certain types of ovarian and uterine cancer, it may be helpful to test their DNA for any errors that can cause cancer. There are lots of important pieces of information to share when someone is diagnosed with cancer, and we are exploring a new way to share information. Patients with certain types of ovarian or uterine cancers will watch a short video that explains what genetic testing is and why it is so important. They will fill out a survey about what they think about the video and if the information is helpful.

The purpose is to recruit potential subjects for ongoing active research projects within the PRIME Lab

The purpose of the study will be to explore the perceptions surrounding parental support and rejection through surveying Chinese or Taiwanese-American young adults that identify as LGBTQ+ (lesbian, gay, bisexual, transgender, queer/questioning, or other non-heterosexual or non-cisgender identity).

We are interested in how people react to offers of help from potential relationship partners.

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.