HIV Research

Active Research

 

HIV/AIDS Research

Research is vital to academic medicine for educating doctors and biomedical scientists, discovering the causes and cures of disease, and translating that knowledge to patient care.

-Immunopathogenesis of HIV/HCV coinfection with a focus on the innate immune response

-Basic immunologic mechanisms underlying EBV latency and EBV/HIV co-infection leading to tumorigenesis

-Immune response and latency during HIV infection

 

Questions about research participation?

• DO I QUALIFY TO PARTICIPATE IN THE RESEARCH?

  To participate, you must: 

  • Be 18 years old
  • Donate a blood sample
• WHAT IS THE STUDY ABOUT AND WHY ARE WE DOING IT?

  We are asking you to choose whether to volunteer for a research study that is unfunded and isintended to create a repository of human specimens for use in research. This initial informationis to give you key information to help you decide whether to participate. We have included detailed information after this information. Ask the research team questions. Taking part in this study is completely voluntary.

   

• WHAT IS THE STUDY ABOUT AND HOW LONG WILL IT LAST?

  By doing this study, we hope to establish a large repository of patient specimens related to human diseases for use in future research studies. Such specimens help us to learn how your body’s immune system deals with infections and inflammation. Your participation in this research will last only until you have provided a specimen to be placed in the repository.

• WHAT ARE KEY REASONS YOU MIGHT CHOOSE TO VOLUNTEER FOR THIS STUDY? 

  You will not directly benefit from this study, but the collection of your specimens may contribute to key research conducted in future health-related studies.

• WHAT ARE KEY REASONS YOU MIGHT CHOOSE NOT TO VOLUNTEER FOR THIS STUDY?

  You may not want to volunteer for this study if you do not want your specimens used for research. The alternative is not participating in this research study. 

• DO YOU HAVE TO TAKE PART IN THE STUDY?

  If you decide to take part in the study, it should be because you really want to volunteer. You will not lose any services, benefits or rights you would normally have if you choose not to volunteer.

• WHAT IS EXPECTED IF I TAKE PART IN THIS STUDY?

  For blood draws, less than 50mL of blood will be drawn and transferred into appropriate tubes. Any bleeding can usually be controlled with a chemical that stops bleeding and by applying pressure. The blood draw site is then covered with a bandage.

• WHAT POSSIBLE RISKS OR DISCOMFORTS MIGHT I HAVE IF I TAKE PART IN THIS STUDY?

  This study may involve collection of a blood specimen. This collection will almost always involve collecting the specimen at the time you are already having blood drawn so that there is not an additional needlestick. There may be some discomfort, bruising, or bleeding at the site where the blood is drawn. Rarely, fainting occurs because of drawing blood.

  *Risks of the usual care you receive are not risks of this study.

• HOW WILL MY PRIVATE INFORMATION BE PROTECTED?

  Every attempt will be made to see that my study results/data are kept confidential. A copy of the consent and data collection form will be stored on a HIPAA-compliant ETSU RedCap server in accordance with the record control schedule. Your medical records will be kept completely confidential according to current legal requirements, and will not be revealed unless required by law, or as described in this form.

 

Clinical Trials

The COE in HIV/AIDS is actively pursuing opportunities for clinical trials for our patients. At this time, we don't have active trials available. However, current opportunities exist here: https://clinicaltrials.gov/

 

For more information about research at CIIDI, contact: