This study aims to understand how rural women experience the expansion of oil palm crops, particularly in the Colombian Llanos region. The research will delve into the work women performed in the plantations and on their own farms. The study also wants to address how women interact with their environment (their practices, what they know about nature, how they use nature) and if that has changed because of the expansion of oil palm. Finally, the research will also explore how the government is helping those women and their families to achieve their dreams. This research is important because there is very little information about rural women living in this region in Colombia. My research will contribute to know more about their stories and highlight their important contribution to the country.

The purpose of this study is to collect data from patients, caregivers, and VAD coordinators to ascertain the stressors associated with having a Ventricular Assist Device (VAD) and use that data to create support groups.

To create digital tools to support young adult cancer survivors completing active treatment and transitioning into survivorship care.

The purpose of this research study is to collect data about attitudes towards social topics in the news.

The purpose of this research study is to test a set of interventions designed to improve HIV care and prevention among girls and young women in Zambia.

The United States is facing a worsening physician shortage that particularly affects people living in rural or underserved communities. One strategy used to address this problem is clinical exposure programs for students in high school, college, and/or medical school. Research currently suggests that these programs could influence participants' interest in medicine, specialty choice, and practice location preferences. Mentoring in Medicine is a summer clinical exposure program that targets college students in the Johnstown area of Pennsylvania. This region of the state is socioeconomically disadvantaged and medically underserved. No formal follow-up has been conducted on the participants since the program began in 2004. We plan on surveying these past participants to examine their academic and career interests and outcomes. We will also use physician databases to determine career outcomes. This data will help contribute to the body of evidence regarding educational interventions to improve medical shortages in the United States.

To collect research samples from CF patients already having a clinically indicated colonoscopy. We're collecting a few additional samples on top of what is collected for clinical purposes to give to researchers for future projects. This will increase your time of procedure around 5 minutes.

The study is designed to look at Crohn's disease over a period time, from before a surgery to 12 months after the surgery has taken place. The role bacteria in the gut plays in Crohn's disease (CD) is not well understood. Which particular microbes contribute to disease remain unknown. In CD, ~70% of patients will end up requiring surgery due to chronic unrelenting complications, and ~50% require additional surgery. We hope to identify key microbes at the time of surgery in stool and tissue and correlate it over time with data collected at timepoints after surgery. We will use this data with clinical information to determine if specific microbes are associated with disease recurrence.

Why have our societies become so polarized? How deeply are we divided? And what is the role of social networks in bridging as well as deepening these divides? This study focuses on local communities in North Carolina to understand political change in America and beyond. In particular, we are interested in how people in their church congregation experience political and social change. This is because churches are pillars of local community life in North Carolina. We reach out to local faith leaders across the spectrum of Christian churches to get their take on how their congregation grapples with the issues of our time. This is part of a comparative study across several Western societies.

The purpose of this Heart Failure Research Registry is to collect relevant patient-level demographic, clinical, laboratory and hemodynamic data from CardioMEMS patients to advance scientific knowledge about pulmonary hemodynamics and heart failure therapies.