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IRB Information for Participants and Patient Advocacy Groups

Advarra’s institutional review board (IRB) strives to protect participant rights and welfare throughout the research process.

Advarra’s IRB reviews clinical research involving human participants. We help ensure participant rights and welfare are protected throughout the research process. As part of our mission to “advance clinical research – safer, smarter, and faster,” we partner with stakeholders throughout the research community to help improve the way researchers safeguard participants.

Advarra’s staff members are available to answer any questions you may have about your rights as a research subject and/or concerns or complaints regarding the research study.

Participant FAQ

Advarra believes in the importance of providing study participants and advocacy groups with the best information available to help them decide if a clinical study is right for them or their group members. Advarra assists clients worldwide in helping participants understand clinical research to more securely access and share information.

What is a clinical trial? Why are studies done?

Before a new treatment is approved and put on the market, it must undergo rigorous testing to ensure it is safe and effective. This testing is conducted as part of a clinical study, during which volunteers are given the prospective treatment — under strict guidelines and regulations that the researchers must follow. Besides safety and efficacy, clinical studies help researchers determine how much improvement the treatment offers participants, the proper dose and dosage form, how long the treatment takes to cause an improvement, and much more.

Without clinical research, there can be no new treatments. Clinical studies are essential to advance health care.

How are study participants protected?

Clinical studies and the study doctors who work in them are regulated by the US government. The law requires that every study be reviewed by an independent group of scientists and community members, whose job is to make sure that the study is as safe for the volunteers as possible. This group is called an institutional review board or IRB.

You might consider volunteering for an IRB — these boards need community members and always need help to review studies. The IRB looks at the plan for the study (called the research protocol) before anyone can join the study. They may ask for changes in the study to make it safer for the people who participate. The IRB also looks at the participants’ confidentiality and privacy. If you join a study, measures must be in place to protect your private health information as well as your name and contact information. Your information will not be in any of the reports about the study. If new information that may be important to you and your decision about the study — especially information about safety — is discovered during the research, you will be informed.

Why join a study?

People have many reasons for joining a study. Some people like the feeling that, by joining, they are helping make new treatments available for all. They may feel that they are helping to improve medical care for the next generation. Many studies include health education and medical tests, which some people like to have and join a study for this reason. Some studies need participants who are suffering from a disease or condition. In these cases, these people often participate in hopes of finding a better treatment.

What are the risks?

A study medicine is an untested or limited tested medicine. Clinical studies are done to test the study medicine or treatment. It is important to talk to your doctor and the study doctor about the study. Ask them what is known and what risks they see. And, when you have asked them all your questions, ask them what else you should ask.

All medicines have unpleasant side effects. Some people may experience the side effects, and others may not. Ask the study doctor about the kinds of side effects that may happen in the study.

The study likely will require appointments with the study doctor. Make sure that the schedule is convenient for you. If it isn’t convenient, ask the study doctor if it can be more flexible. These appointments are important for checking the effects of the study medicine on your health. Additionally, some studies may require overnight stays. Rest assured, researchers are required by law to tell what is required before you agree to participate.

What are placebos?

A placebo is an inactive substance. Studies use placebos to compare against a drug or treatment to check the effectiveness of that drug or treatment.

What are combination products?

If a proposed treatment has both a drug (or biologic) and device component, the FDA may consider it a combination product.

Examples of possible combination products are asthma inhalers, drug delivery patches, collagen implants, and drug-eluting stents. The FDA may decide to treat a combination product as a drug or as a device, and that determination will affect the IRB review.

How do I decide?

Talk with the study doctor and with your own doctor. Ask the study doctor to explain the study — including any details you would like to know. Be certain you ask all your questions. The study staff want you to feel comfortable with the study. Here are some questions you may want to ask:

  • What will I have to do in the study?
  • How long will it last?
  • How many times will I have to come for study appointments?
  • How long will the study appointments last?
  • Who will be watching out for my health?
  • What are the risks in the study?
  • Will my transportation and parking be reimbursed?

Again, once you have asked every question you have, ask the study doctor what else you should ask.

What is informed consent?

The US government oversees medical studies that include people. One law ensures that no person can be forced to be in a clinical study or join against their will. Another law requires researchers to make sure that the people who join understand what to expect. Any person who joins a research study must consent to join, and that consent must be “informed.”

The study staff or doctor will give you an informed consent form to explain the study. Please take your time to read and understand it and be sure to ask about anything you don’t understand. If you like, you may take it home and have a family member or your doctor look at the form. If you decide to join the study, the study staff or doctor will ask you to sign the form to show that you understand what has been explained about the study. You will also be given a copy of the informed consent form to take home and keep.

Responsibilities

Everyone who joins a clinical study has responsibilities to the study. These are some of the important responsibilities that study volunteers have:

  • Come to the study appointments on time. If you have a conflict, please call and reschedule.
  • You may be asked to take a medication or fill out forms at home. Please try to do this on schedule and follow the study doctor’s instructions.
  • Always try to be honest when answering questions. If you had a headache, it is important for the study staff to know. If you don’t feel better, tell them. They want to know the truth. Ask the study staff what other responsibilities you may have in the study.

Rights

Everyone who joins a clinical study has rights. Ask the study staff about your rights in the study. The informed consent form will also tell you about your rights. Some important rights are:

  • You do not have to join a study.
  • If you join, you can change your mind. You may leave a study at any time.
  • You have a right to ask questions and have them answered to your satisfaction.
  • Some studies reimburse volunteers for their time and transportation costs.
  • You have a right to confidentiality and privacy. Your name and contact information will not be on any study report.

You may have questions about a specific study, an injury that you think might be related to research, the instructions you received, or a payment. Ask the study doctor or staff all your questions. If you have questions about your rights, or if you have complaints, you can also contact the IRB listed on your copy of the informed consent form.

What should I do if someone asks me to consider a study for my child?

Talk to your child’s doctor. No one knows your child’s health better than their doctor. If your child’s doctor is not the study doctor, they may want to consult with the study doctor. Get all the information you need to help you decide whether the study may be a good idea for your child.

Where do I go if I am looking for a study for my child?

Ask your doctor. Search the internet. If your child has a chronic or serious disease, you may be able to find information from a support group for that disease.

Will my child be safe in a study?

Government regulations require that studies including children receive special scrutiny. The IRB will carefully evaluate a study of children to assess the risks compared to potential benefits.

What else should I consider about potentially enrolling my child in a study?

Ask your child. Explain the reasons for the study and what they will have to do. If you have questions, ask the study doctor, and ask them to speak with both you and your child. If your child doesn’t want to be in the study, don’t try to persuade them. No one should ever feel forced to join a study — including your child.

How do I learn more about clinical research?

Visit the links below for more information:

  • The Center for Information and Study on Clinical Research Participation is a nonprofit organization that works to help the public understand clinical research. ciscrp.org

To find lists of US clinical research studies:

  • Clinical studies are listed on a website run by the US government. You can use this site to find a study. clinicaltrials.gov
  • The National Cancer Institute lists cancer studies on its site. cancer.gov/clinicaltrials
  • The US Department of Veterans Affairs also works to educate veterans about clinical studies. research.va.gov/default.cfm
  • The National Health Council is a group that works to improve health across the country. Its membership represents a breadth of disease-specific participant advocacy groups. nationalhealthcouncil.org

To find lists of Canadian clinical research studies:

  • Health Canada’s Clinical Trial Database provides a public listing of Phase I, II, and III clinical trials. health-products.canada.ca/ctdb-bdec/index-eng.jsp
  • Health Canada encourages sponsors to register studies on ClinicalTrials.gov (run by US NIH).  clinicaltrials.gov
  • The Canadian Institute for Military and Veteran Health Research (CIMVHR) works to educate veterans about clinical studies and research. cimvhr.ca

Most medical schools offer information on clinical studies. You can also find information about research studies by searching the web for the participant support groups that meet your specific needs.

Need to contact the IRB with a question or concern as a subject participating in a study? Want to know more about your rights as a research participant?