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ClinicalTrials.gov at UK: Guidelines for Investigators on Clinical Trials Registration and Results Reporting

Session objectives: Review the purpose of ClincalTrials.gov Review which studies need to be registered and discuss how to register your study Describe general requirements and your responsibilities after registration Describe the general requirements for results submission Summarize potential consequences of noncompliance Presented by:Ashley Walton-RobbinsClinical Trials Compliance Administrator 

Clinical Research Coordinator 101

Clinical Research Coordinator 101 is designed for clinical research coordinators, clinical research associates, and staff who function in this capacity. The course introduces the basics of coordinating clinical research at the University of Kentucky and is intended for early-career coordinators or those new to the field.

Power Analysis for Clinical Trials

Presented by:Chris McLouth, PhDAssistant ProfessorDepartment of Biostatistics

An LLM-Driven Robotic Healthcare Assistant with Multi-Modal Environmental Sensing

This presentation details how we enable the Temi robot to function as an autonomous healthcare assistant, exploring the challenges and implications of robotics in healthcare. Presented by:   Evan Damron, Software Developer at the Center for Applied AI, Computer Science Graduate Student, University of Kentucky Event page

UK researchers enrolling patients in trial to address rare pregnancy condition

Researchers at UK HealthCare are now enrolling patients in the phase 3 AZALEA trial to evaluate the safety and efficacy of an investigational medication in pregnancies at risk for severe hemolytic disease of the fetus and newborn (HDFN).

Translating Science to Policy in AppalTRUST: A Tobacco Center on Regulatory Science

This presentation will provide an overview of AppalTRUST, the University of Kentucky Tobacco Center on Regulatory Science. This integrated center is recruiting 2000 Appalachian adults to learn about tobacco product use patterns and provide the Food and Drug Administration with guidance on effective tobacco-related policies in this region.

Introducing Advarra eReg: CRSO's New Electronic Regulatory Management System

Objectives: To share key features and demonstrate functionality of the Advarra eReg system: 

BERD & CCTS Pilots: What You Need to Know before You Submit

Session Summary: In this session, CCTS members will present on BERD's role in the CCTS Pilot submission process. Dr. Joel Thompson will discuss the CCTS Pilot submission process and the incorporation of a BERD review with the proposal. Dr. Kelsey Karnik will discuss the process of the BERD review, including analytical tips when writing the proposal and how to incorporate BERD feedback. Dr. Emily Slade will discuss how to involve quantitative collaborators when a CCTS Pilot is awarded.   

REDCap Training Series: Advanced

This training is intended for those who are familiar with the basic features of REDCap. The session will cover building a longitudinal research project in REDCap.      Objectives:   Understand calculations   Import data   Explore new dashboard features   More information here.

REDCap Training Series: Intermediate

This training is designed for REDCap users who already know how to navigate the program and create a basic survey.    Objectives:   -Become familiar with arrangement of projects and set up in REDCap   -Create a multi-survey project   -Understand E-Consent and IRB considerations   -Use REDCap reports and reporting features More information here.