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Division of Research
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    Streamlining research processes at UTRGV. Access tools and guidance for compliance, proposal submissions, funding, and more

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    The Division of Research at UTRGV is dedicated to advancing and supporting the university's research activities, benefiting students, faculty, and staff.

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    The Analytics Hub provides centralized access to key tools like ARGO, Control Tower, Data Pulse, DPM, and Academic Analytics, empowering data-driven decisions across research, academics, and operations at UTRGV.

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    Research Communications enhances the visibility and impact of research activities across UTRGV. Our mission is to ensure that UTRGV’s research reaches both internal and external audiences, enhancing the university’s research reputation.

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    Discover UTRGV’s Division of Research, supporting high-impact research and scholarship across all disciplines.

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  6. For Research Participants
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Institutional Review Board (IRB) Menu

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  • Researcher's FAQs
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  • Researcher Participants FAQs
  • IRB Education & Guidelines

Contact Us

Christy Richardson, CIP
Sr. IRB Coordinator
irb@utrgv.edu

Mariana Hernandez, MPA
IRB Coordinator
irb@utrgv.edu
956-665-3598

Quick Links

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For Research Participants

  1. What is the research about and why is it being done?
  2. What do researchers hope to learn and who might benefit from it?
  3. Who is funding the study?
  4. Who has reviewed and approved the study?
  5. Who is being asked to volunteer to be in the study?
  6. Why are you, specifically, being asked to participate?
  7. When is the study expected to be completed?
  8. How will the findings of the research be shared and would you be informed personally?
  9. What kind of study is this?
    1. Is it a clinical trial?
    2. How many groups (or arms) are there?
    3. Is assignment to groups randomized, or could you choose?
    4. Will any of the groups receive a placebo or an inactive treatment?

  1. What would you have to do? What kind of medications, procedures, or tests would you have?
  2. Will you have to go anywhere to participate in the study?
  3. Will the study involve a novel or untested intervention that is considered experimental?
  4. Would you be told if you are given the intervention being tested?
  5. How long would your participation last?
  6. Would you be given the results of any study tests or procedures that are done?
  7. If you have a disease or condition that is being studied in the research and you choose not to participate, what treatments or procedures are available to you? Would you still have access to the research intervention outside of the study?
  8. If you have a disease or condition that is being studied in the research, ask if your doctor is also a researcher on the study. If so, who would watch out for your best interests as a patient?
  9. How would being in this study affect your daily life?
  10. How would being in this study affect your current medical care?

  1. How much do the researchers know about the risks of the research intervention–especially if the intervention is novel or experimental? Does the intervention have FDA approval or oversight?
  2. What are the short- or long-term risks, discomforts, or unpleasant side effects?
  3. What are the researchers doing to minimize risks, discomforts, or unpleasant side effects?
  4. Is there anything you could do to minimize your risks during the study?

  1. How would your biological materials (such as blood samples), data (such as test results), or other personal information be used or shared?
  2. How would your privacy and identifiable private information be protected?
  3. What could happen to you if your identifiable private information were disclosed to others?

  1. Will participating in the study cost you anything? For example, would you have to pay for certain tests or procedures, or the study drug? If so, what is the estimated cost and would it be covered by health insurance?
  2. If you were harmed while participating in the study, who would pay for the necessary medical care?
  3. Will there be any travel or other study-associated costs (for example, child care) and will researchers provide any money to cover those costs?
  4. If the research offers financial compensation, how much is offered and when would you receive it?

  1. Would you, personally, benefit from participating in the research? If so, how?
  2. How much time will you have to think about your options before making a decision?
  3. If your doctor is also the researcher on the study and you decide not to participate, would this decision affect your current medical care?
  4. Who should you contact if you have questions about participating in the research?
  5. Who should you contact if you have concerns about the research itself?
  6. What happens if you volunteer to participate now, but decide to quit the study later?

The U.S.Department of Health & Human Services' (HHS) Office for Human Resource Protection (OHRP) has created a series of short videos with basic information about research. These videos are intended to help potential participants understand how research works, what questions they should consider asking, and things to think about when deciding whether to participate in a study.

video 1 - what is research Part 1: What is Research?
This video provides basic information about scientific research, the goals of research, and discusses how clinical research differs from medical care. (3:00)

video 2 - clinical trials Part 2: Clinical Trials
This video discusses types of human research with a focus on clinical trials, and explains common terms that potential participants should know. (4:20)

video 3 - ask questions Part 3: Questions to Ask
This video emphasizes that participating in research is voluntary and encourages potential participants to ask questions and get the information they need to decide whether to participate. (4:44)

video 4 - randomization Randomization
This video explains the concept of randomization in research studies and what potential participants need to know when volunteering for a study with a randomized design. (7:25)

video 5 - institutional review boards Institutional Review Boards (IRBs)
This video explains the concept of Institutional Review Boards (IRBs), which review certain research studies involving human volunteers to ensure that the studies meet ethical standards and regulatory requirements. (6:45)

video 6 - behavioral research Participating in Social & Behavioral Health Research
This video provides basic information about social and behavioral health research and what makes it different from clinical research. (6:05)


Research Match Banner

Research Match

ResearchMatch is a national volunteer research registry that brings together researchers and willing volunteers who want to get involved in research studies. It was developed by institutions affiliated with the Clinical and Translational Science Awards (CTSA) program and provides a secure, web-based approach to address a key barrier to advancing research: finding research participants.

Looking to volunteer for ResearchMatch? Check out more information here or register on their website.

Volunteers can register for ResearchMatch at researchmatch.org – it only takes 5 to 10 minutes to register. Volunteers of any age, race, ethnicity, and health status are invited to join. By registering in ResearchMatch individuals are not registering to participate in any study. They are showing interest to be contacted about studies that may be a good ‘match’ for them. The goal of ResearchMatch is to better connect volunteers with potential study opportunities.

Division of Research


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research@utrgv.edu
BBRHB 2.210

(956)-296-1549

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research@utrgv.edu
ESSBL 5.110

(956)-665-3883

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