Timely diagnosis and treatment for breast cancer was enhanced through $350,000 in grants from the Health Sciences Foundation. A new digital mammography unit purchased for the Linda Buchan Centre is capable of exact and accurate placement of the needle for the tissue sample for breast biopsy.
Clinical research plays an extremely important part in healthcare at the Thunder Bay Regional Health Sciences Centre. As an academic health sciences centre, we are literally a centre for learning for researchers, students, teachers, and other healthcare professionals.
But that’s not why we do it. We emphasize research and training at the Health Sciences Centre because it leads to better patient care, today as well as tomorrow. We’ve attracted researchers from around the world to Thunder Bay to work at the Health Sciences Centre and/or the Thunder Bay Regional Health Research Institute (TBRHRI), the research arm of the Health Sciences Centre (find out more at www.tbrhri.ca). Together, we’re partnering with other world-class researchers at Lakehead University, the Northern Ontario School of Medicine, and others, developing tomorrow’s healthcare techniques and equipment right now.
In turn, we’ve attracted some of the best physicians and other healthcare providers who want to work in our academic environment. Every year, we’re drawing students to Northwestern Ontario who want to train here, making them more likely to stay and practice here too.
Clinical trials in particular have a positive impact on patient care, and are an important part of any research program. Clinical trials are research studies investigating new treatment methods, medications, medical devices, equipment, and/or medical conditions themselves to improve care for future patients. There are dozens of clinical trials underway at the Health Sciences Centre at any given moment.
Patients may be asked if they are interested in participating in clinical research when they are admitted to the Thunder Bay Regional Health Sciences Centre. Alternatively, it may also be suggested to you by your primary care provider or specialist, or you may also actively search out a clinical trial on your own. No matter how you learn about these research studies, it’s important to note that you have the right to refuse participation in any clinical trial and you will not lose any of the benefits to which you would otherwise be entitled. Also, clinical trials have a screening process to ensure patients meet certain criteria or conditions, so you may not be accepted into a clinical trial in some cases. Common criteria for inclusion or exclusion include age, sex, type of medical condition, existence of other medical conditions, and current treatment plans.
Once you have indicated that you are open to participating in a clinical trial, a member of the research team will review your chart to see if you are eligible for an ongoing trial.
An important part of the clinical trials process is your informed consent, and you will have to sign a form for that clinical trial to join the study. A member of the research team will go over all the risks and benefits of participating in the study with you (some general risks and benefits are outlined below). This is also an opportunity for you to ask some of your own questions, including:
If you decide to join the trial, a member of the research team will describe the next steps with you, which vary depending on the study. For example, if the study is comparing two drugs, or the effects on patients with or without the drug, you will be randomly assigned to the test group or to a control group. After that, you simply have to follow the directions given to you and attend any appointments made for you. You will have the opportunity to contact the Clinical Research Services Department anytime with questions you may have.
Patients who enroll in a clinical trial may benefit directly, as you’ll read below. However, you will not be paid for joining a clinical trial except for the possible reimbursement of any expenses associated with the clinical trial.
Clinical trials have their own set of benefits and risks. A member of the research team and/or members from your own healthcare team will explain the specific benefits and risks of the clinical trial you are considering joining. Here are some general things to think about:
Your health always comes first. We do everything to ensure you get the best care possible during your participation in any clinical trial. However, there are some drawbacks to joining a clinical trial that you should consider as well:
Every clinical trial, whether it is developed here in Thunder Bay or is part of a larger national or international trial, is carefully reviewed by our Research Ethics Board to ensure that it is safe, offers potential benefit to patients, and is conducted in an ethical matter. For more information, please contact the Research Ethics Office directly at REO@tbh.net or (807) 684-6422.
Participating in a clinical trial is always voluntary, and you should never feel pressured to join any clinical trial. After you find out the information about the trial and consider your options, it is totally acceptable to say no.
For more information about clinical trials please contact the Clinical Research Services Department at (807) 684-7566. You can also find a list of most current clinical trials at the Health Sciences Centre here: http://clinicaltrials.gov/ct2/results?term=Thunder+Bay&recr=Open
(Note: some programs at the Health Sciences Centre are directly enrolled in certain clinical trials. Ask you specialist for more information.)
The Health Sciences Centre and the Health Research Institute work closely with industry partners. There are many benefits:
With a strong clinical trials infrastructure in place since the 1980s and our unique research opportunities, we continue to attract industry partners from around the world.