Participating in a clinical trial allows patients to receive potentially ground-breaking treatment or therapies that are currently in development, advancing the frontiers of scientific knowledge and treatment of disease. Clinical trials are important to develop new therapies and treatments. Most of the standard treatments accepted and used by doctors today are based on the results of previous clinical trials.
Clinical trials are strictly controlled research studies conducted on people. Each study is carefully designed to answer specific questions about a new treatment like a drug or a medical device to make sure it is safe and effective to use in people.
The details of the clinical trial, including all the tests and procedures used in the study, are outlined in a research plan, also called a protocol. The doctors, nurses and scientists who run the clinical trial must follow the protocol and run the tests according to the strict rules set by the Food and Drug Administration (FDA) and other government agencies. The rules ensure that people who participate in the clinical trial are treated as safely as possible.
A breadth of laws and regulations exist, as well as the ethical commitment of the research sponsors and institutions, to treat all patients with respect, beneficence and justice to protect any patient who participates in clinical research. An Institutional Review Board (IRB) is in place at St. Vincent to ensure that these commitments are upheld.
If you are currently enrolled in a clinical study at any St. Vincent location and you have questions about the study, please call the study's Principal Investigator (the physician managing your research care).
If you do not know how to contact the Principal Investigator, please call the St. Vincent Research and Regulatory Affairs office at 317-338-2194 or e-mail us at firstname.lastname@example.org
The US National Institutes of Health offers a comprehensive list of both open and closed studies at:
Search for only current open studies at St. Vincent
If you are interested in learning about studies underway at St. Vincent Health that are currently recruiting participants, please call our office at 317-338-2194 to discuss availability.
I have been asked to participate in a research study. Before I make a decision on whether or not I want to participate in this study, I have the right:
If you are interested in learning about studies underway at St. Vincent that are currently recruiting participants, we invite you to call our office at 317-338-2194 to discuss options available.
The US National Institutes of Health also offers a comprehensive list of both open and closed studies at its website:
There are many resources that contain valuable information and education about clinical research and ongoing clinical research trials. Below are links that will connect you with more information:
Volunteering to be in a research study is an important decision. Some common questions are listed below to help you get ready for the discussion you will have with the researchers. Not all of the questions apply to every study.
Remember: You have the right to get all your questions answered. If you do not understand the answer, ask the question again.
A clinical trial is a strictly controlled research study conducted in people. Each study is carefully designed to answer specific questions about a new treatment like a drug or a medical device to make sure it is safe and effective to use in people.
The details of the clinical trial, including all the tests and procedures used in the study, are outlined in a research plan, also called a protocol. The doctors, nurses, and scientists who run the clinical trial must follow the protocol and run the tests according to the strict rules set by the Food and Drug Administration (FDA) and other government agencies. The rules ensure that people who participate in the clinical trial are treated as safely as possible
Clinical trials are important to develop new therapies and treatments. Many of the standard treatments accepted and used by doctors today are based on the results of previous clinical trials.
Clinical trials are sponsored or funded by a variety of organizations or individuals such as medical institutions, foundations, voluntary groups, pharmaceutical companies and federal agencies such as the National Institutes of Health (NIH). Trials can take place in a variety of locations, such as hospitals, doctors´ offices, or community clinics.
A protocol is a study plan on which all clinical trials are based. The plan is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by the research staff to monitor their health and to determine the safety and effectiveness of their treatment.
Clinical trials are conducted in phases. The trials at each phase have a different purpose and help scientists answer different questions:
An Institutional Review Board, also called an IRB, is a committee of doctors, scientists, and people from the community where the clinical research is taking place. An IRB reviews the clinical research plan to make sure people in the research study will be treated fairly and that any risks will be explained to them.
Before a clinical research study can begin, the research plan must be approved by an IRB. IRB questions, questions about the research, questions about research participant rights, complaints or concerns can be directed to the Office of Research Protection at 713-441-7548.
People who volunteer to participate in research come from all walks of life. Volunteers may be healthy and participate in clinical research, or they may be patients or other people with health problems.
People with a specific type of medical condition or disease may be asked to volunteer for a research study because doctors want to learn more about their condition or there may be a promising new treatment being studied.
Because disease and life-threatening conditions affect everyone regardless of race, gender, age, and national origin, volunteers are needed for many types of research studies.
Yes. Just like for studies with adults, there are guidelines explaining who can take part. The child´s parent or guardian needs to give permission for their child to participate. If the child is an adolescent or old enough to understand what the study is about, the child will also be asked to give their assent to take part in the study.
Each study is different. The amount of time a study takes depends on the research questions the study is designed to answer. A study may take a few hours, a few months, or even years to finish.
Participation in a clinical research study has several potential benefits:
Along with benefits, there are potential risks and drawbacks of participating in a clinical research study:
If you think you might want to volunteer for a clinical research study, tell the researchers you are interested in learning more. Someone from the research team, usually the principal investigator (the physician in charge of the study) or a trained staff member will explain the details of the study to you. The information must include the following:
During this discussion you should ask as many questions as you want in order to fully understand the details of the study. Take as much time as you need to make your decision. You may want to ask family members or friends to read the consent form.
If you decide to participate in the research study, you will be asked to sign the consent form.
If you agree to participate, and after you sign the consent form, you may be asked to take part in screening tests to make sure you qualify for the research study. Researchers use a set of guidelines to help them select volunteers for the clinical research study. They want to make sure it is okay for volunteers to participate.
Informed consent is a process of learning the important facts about the clinical trial to help people decide whether to participate. Informed consent is a process throughout the study to provide ongoing information for participants. After learning about the study, participants will be able to ask the researcher or his/her research staff questions. People should only agree to take part in a study if they clearly understand the study and feel comfortable. If they agree to take part in the study, they will be asked to read and sign an "informed consent form". Signing the form does not require patients to stay in the study. Participants can leave the study at any time during the study or the follow-up period.
Volunteering to be in a clinical research study is an important decision. For a list of general questions about taking part in clinical research, see below. Not all the questions on the list will apply to the clinical study you are thinking about.
|Questions That Apply to Most Research Studies||Questions That Apply to Most Treatment Studies|
|What is the purpose of the study?||Has the study treatment been tested in humans?
If so, what was learned?
Who is conducting the study?
|How long will the study last?||Is there a real and fake (placebo) treatment?
Will I know what I´m getting?
|Who has reviewed and approved the study?||Who has reviewed and approved the study?
What are the possible effects of the treatment?
|How will this study affect my daily life?
What will happen to me?
|What is the standard of care for my condition?|
|Will I be paid to be in the study?||Who will be in charge of my care?|
|Will I be reimbursed for any expenses?||Will my health insurance cover any of the costs?
What will I have to pay?
|Who will know I am taking part in this study?
Who will see my medical record?
|Are there other treatments available for my condition?|
|If I change my mind how do I end my participation in the study?||How long will I receive the treatment?|
|What will happen to me at the end of the study?||Can I choose to stay on the treatment after the study ends?|
|Will I be told the results of the study?||What happens if I am harmed by the study treatment?|
|Whom do I contact for questions and information about the study?||Will I be able to take my regular medications?|
YES. If you decide to be in a study now and you change your mind later, that is okay. You just have to tell the study doctor or the study staff as soon as you change your mind. They may ask you to come back for a final visit to check your health.
It is always your choice to participate, or not to participate in a research study. Whether you are a healthy volunteer or you have an illness, you will want to find out all the details of the study before deciding to participate or not.
Financial arrangements are different for every research study. Research costs, such as the cost of hiring personnel and managing data, are covered by the organization paying for the clinical study. Some research studies will pay you for joining the trial, but many will not pay you for participating. Some studies will reimburse some of your expenses, such as transportation and parking fees.
Costs for some studies, like clinical trials for drugs and implantable medical devices, may be charged to you or your medical insurance. You should seek more information about the financial arrangements from the clinical research team and from your insurance provider.
Information about you and your participation in a research study will be kept as confidential as possible. Information will be given only to those who have permission to see your records. This may include the group sponsoring the study and those who make sure the study is safe and carried out according to the research plan. Some studies are reviewed by the Food and Drug Administration (FDA).
Researchers review and analyze data collected during the research study. Results of clinical studies are sometimes published in medical journals, but your identity will not be revealed.
A single research study may take place at many different medical centers at the same time. After the study has been completed, all the information is send to one central place to be analyzed. If the study was sponsored by a government agency, such as the National Institutes of Health, officials from the agency will review the study information.
If the clinical study was conducted to get FDA approval for a new drug or medical device, the completed data will be submitted to the FDA for review. If the FDA fids the treatment to be safe and effective, the agency may approve the treatment for use in the general public.